NUCLEIC ACID MODIFICATION WITH TOOLS FROM OXYTRICHA

Abstract

The present disclosure provides, inter alia, methods for treating a disease characterized by an abnormal level of m6dA in a subject, such as cancer, methods of modifying a nucleic acid from a cell, methods for identifying protein binding sites on DNA, methods of mediating DNA N6-adenine methylation, methods of modulating nucleosome organization and/or transcription in a cell, using MTA1c or any components thereof. The present disclosure also provides methods of generating a synthetic chromosome and synthetic chromosomes made by such methods. Pharmaceutical compositions comprising MTA1c or any components thereof and kits containing such compositions or for carrying out such processes are further provided. Eukaryotic cells, vectors and transgenic organisms comprising MTA1c or any components thereof are also provided. Synthetic chromosomes and methods of making same are also provided.

Claims

1. A method of treating or ameliorating the effects of a disease characterized by an abnormal level of m6dA in a subject, comprising administering to the subject an amount of MTA1c or any components thereof effective to modulate m6dA levels in the subject.

2. The method according to claim 1, wherein the modulation comprises restoring m6dA levels to normal or near-normal ranges in the subject.

3. The method according to claim 1, wherein the disease is a cancer.

4. The method according to claim 3, wherein the cancer is gastric cancer or liver cancer.

5. The method according to claim 4, further comprising administering to the subject one or more of anti-gastric cancer and anti-liver cancer drugs.

6. The method according to claim 1, furthering comprising co-administering to the subject an epigenetic agent.

7. The method according to claim 6, wherein the epigenetic agent is selected from the group consisting of methylation inhibiting drugs, Bromodomain inhibitors, histone acetylase (HAT) inhibitors, protein methyltransferase inhibitors, histone methylation inhibitors, histone deacetlyase (HDAC) inhibitors, histone acetylases, histone deacetlyases, and combinations thereof.

8. A pharmaceutical composition comprising MTA1c or any components thereof that is effective to modulate m6dA levels in a subject in need thereof and a pharmaceutically acceptable carrier, diluent, adjuvant or vehicle.

9. A method of modifying a nucleic acid from a cell, the cell derived from a multicellular eukaryote, comprising the steps of: (a) obtaining the nucleic acid from the cell; and (b) contacting the nucleic acid with MTA1c or any components thereof under conditions effective to methylate the nucleic acid.

10. The method according to claim 9, wherein the methylated nucleic acid is effective to modulate nucleosome organization and transcription.

11. The method according to claim 9, wherein the modification is a DNA N6-adenine methylation.

12. The method according to claim 11, wherein the DNA N6-adenine methylation is one or more of dimethylated AT (5′-A*T-3′/3′-TA*-5′), dimethylated TA (5′-TA*-3′/3′-A*T-5′), dimethylated AA (5′-A*A*-3′/3′-TT-5′), methylated AT (5′-A*T-3′/3′-TA-5′), methylated AA (5′-A*A-3′/3′-TT-5′), methylated AC (5′-A*C-3′/3′-TG-5′), methylated AG (5′-A*G-3′/3′-TC-5′), methylated TA (5′-TA*-3′/3′-AT-5′), methylated AA (5′-AA*-3′/3′-TT-5′), methylated CA (5′-CA*-3′/3′-GT-5′), and methylated GA (5′-GA*-3′/3′-CT-5′).

13. The method according to claim 9, wherein the MTA1c or any components thereof comprises a mutation effective to abrogate dimethylation of the nucleic acid.

14. The method according to claim 13, wherein the mutation comprises loss of a C-terminal methyltransferase domain.

15. The method according to claim 9, wherein the MTA1c or any components thereof is obtained from ciliates, algae, or basal fungi.

16. The method according to claim 9, wherein the MTA1c or any components thereof is obtained from Oxytricha or Tetrahymena.

17. A cell line obtained from a multicellular eukaryote comprising a nucleic acid encoding MTA1c or any components thereof and/or an MTA1c protein complex or any components thereof.

18. The eukaryotic cell according to claim 17, wherein the nucleic acid encoding MTA1c or any components thereof is operably linked to a recombinant expression vector.

19. A method of identifying protein binding sites on DNA comprising the steps of: (a) providing DNA; (b) contacting the DNA with MTA1c or any components thereof under conditions effective to methylate the DNA; (c) contacting the DNA with one or more proteins; (d) contacting the DNA with an enzyme effective to hydrolyze the DNA in positions where no protein binding occurs; (e) removing the DNA bound protein; and (f) isolating and sequencing the DNA fragments.

20. The method according to claim 19, wherein the one or more proteins comprise histone octamers.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0023] The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

[0024] The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present disclosure. The disclosure may be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.

[0025] FIGS. 1A-1E show epigenomic profiles of Oxytricha chromosomes.

[0026] FIG. 1A shows meta-chromosome plots of chromatin organization at Oxytricha macronuclear chromosome ends. Heterodimeric telomere end-binding protein complexes (orange ovals) protect each end in vivo. Horizontal red bar: promoter. The 5′ chromosome end is proximal to TSSs. Nucleosome occupancy, normalized Mnaseseq coverage; 6 mA, total 6 mA number; Transcription start sites, total number of called TSSs.

[0027] FIG. 1B shows histograms of the total number of 6 mA marks within each linker in Oxytricha chromosomes. Distinct linkers are depicted as horizontal blue lines.

[0028] FIG. 1C shows that poly(A)-enriched RNA-seq levels positively correlate with 6 mA. Genes are sorted according to the total number of 6 mA marks 0-800 bp downstream of the TSS. FPKM, fragments per kilobase of transcript per million mapped RNA-seq reads. Notch in the boxplot denotes median, ends of boxplot denote first and third quartiles, upper whisker denotes third quantile+1.5× interquartile range (IQR), and lower whisker denotes data quartile 1-1.5×IQR.

[0029] FIG. 1D shows that composite analysis of 65,107 methylation sites reveals that 6 mA (marked with 1 occurs within a 5′-ApT-3′ dinucleotide motif.

[0030] FIG. 1E provides the distribution of various 6 mA dinucleotide motifs across the genome. Asterisk, 6 mA.

[0031] FIGS. 2A-2G show purification and characterization of the ciliate 6 mA methyltransferase.

[0032] FIG. 2A provides phylogenetic analysis of MT-A70 proteins. Bold MTA1 and MTA9 genes are experimentally characterized in this study. Paralogs of MTA1 and MTA9 are labeled as “-B.” Posterior probabilities >0.65 are shown. Gray triangle represents outgroup of bacterial sequences. The complete phylogenetic tree is shown in FIG. 9G. Gene names are in Table 5. Tth, Tetrahymena thermophila; Otri, Oxytricha trifallax.

[0033] FIG. 2B shows the phylogenetic distribution of the occurrence of ApT 6 mA motifs and MT-A70 protein families. Filled square denotes its presence in a taxon. The basal yeast clade is comprised of L. transversale, A. repens, H. vesiculosa, S. racemosum, L. pennispora, B. meristosporus, P. finnis, and A. robustus.

[0034] FIG. 2C is an experimental scheme depicting the partial purification of DNA methyltransferase activity from Tetrahymena nuclear extracts.

[0035] FIG. 2D show gene expression and protein abundance of candidate genes in partially purified Tetrahymena nuclear extracts. UniProt IDs are listed in Table 5. RNA-seq data are from (Xiong et al. 2012). FPKM, fragments per kilobase of transcript per million mapped RNA-seq reads. Low, Mid, and High DNA methylase activity correspond to fractions eluting from the Nuvia cPrime and Superdex 200 columns in FIG. 2C. Total spectrum counts, total number of LC-MS/MS fragmentation spectra that match peptides from a target protein.

[0036] FIG. 2E shows DNA methyltransferase assay using [3H]SAM. Vertical axis represents scintillation counts. Error bars represent SEM (n=3).

[0037] FIG. 2F shows dot blot assay using cold SAM.

[0038] FIG. 2G shows DNA methyltransferase assay performed on different nucleic acid substrates in the presence of MTA1, MTA9, p1, and p2. Sense ssDNA are 5′.fwdarw.3′; antisense are 3′.fwdarw.5′. ApT dinucleotides are labeled in bold red. Horizontal blue lines in hemimethylated dsDNA substrates denote possible locations where 6 mA may be installed by EcoGII (prior to this assay). Relative activity denotes scintillation counts normalized against the unmethylated 27 bp dsDNA substrate with two ApT motifs (top-most dsDNA substrate). An enlarged bar plot of relative activity on 27 bp unmethylated dsDNA substrates is included in FIG. 10K. Error bars represent SEM (n=3).

[0039] FIGS. 3A-3E show genome-wide loss of 6 mA in mta1 mutants.

[0040] FIG. 3A shows schematic depicting the disruption of Oxytricha MTA1 open reading frame. Flanking dark blue bars: 5′ and 3′ UTR; yellow, open reading frame; red, retention of 62 bp ectopic DNA segment; gray bar, intron; Internal light blue bar, annotated MT-A70 domain; ATG, start codon; TGA, stop codon. Agarose gel analysis shows PCR confirmation of ectopic DNA retention.

[0041] FIG. 3B shows dot blot analysis of RNase-treated genomic DNA.

[0042] FIG. 3C shows histogram of 6 mA counts near 5′ and 3′ Oxytricha chromosome ends. Inset depicts histogram of fold change in total 6 mA in each chromosome, between mutant and wild-type cell lines.

[0043] FIG. 3D shows that chromosomes are sorted into 10 groups according to total 6 mA in wild-type cells (blue boxplots). For each group, the total 6 mA per chromosome in mutants and the difference in total 6 mA per chromosome are plotted below. Boxplot features are as described in FIG. 1C.

[0044] FIG. 3E shows motif distribution in wild-type and mta1 mutants. Loss of ApT dimethylated motif is underlined.

[0045] FIGS. 4A-4E show effects of 6ma on nucleosome organization in vitro and in vivo.

[0046] FIG. 4A shows the experimental workflow for the generation of mini-genome DNA.

[0047] FIG. 4B shows agarose gel analysis of Oxytricha gDNA (Native) and mini-genome DNA before chromatin assembly.

[0048] FIG. 4C shows that methylated regions exhibit lower nucleosome occupancy in vitro but not in vivo. Overlapping 51 bp windows were analyzed across 98 chromosomes. For each window, the change in nucleosome occupancy in the absence versus presence of 6 mA was calculated. Boxplot features are as described in FIG. 1C. p values were calculated using a two-sample unequal variance t test. N.S., non-significant, with p>0.05.

[0049] FIG. 4D shows the reduction in nucleosome occupancy at methylated loci in vitro (black arrowheads). For in vitro MNase-seq, +6 mA refers to chromatin assembled on Oxytricha gDNA, while −6 mA denotes chromatin assembled on mini-genome DNA. The vertical axis for SMRT-seq data denotes confidence score [−10 log(p value)] of detection of 6 mA, while that for in vitro MNase-seq data denotes nucleosome occupancy.

[0050] FIG. 4E shows no change in nucleosome occupancy in linker regions despite loss of 6 mA in mta1 mutants. Vertical axes are the same as FIG. 4D.

[0051] FIGS. 5A-5C show modular synthesis of full-length Oxytricha chromosomes.

[0052] FIG. 5A shows features of the chromosome selected for synthesis. Gray boxes represent exons. All data tracks represent normalized coverage except for SMRT-seq, which represents the confidence score [−10 log(p value)] of detection of each methylated base.

[0053] FIG. 5B shows the schematic of chromosome construction. Different colors denote DNA building blocks ligated to form the full-length chromosome. Precise 6 mA sites (bold red) represent cognate 6 mA positions revealed by SMRT-seq in native genomic DNA. These are introduced via oligonucleotide synthesis. For chromosome 5, 6 mA sites (non-bold red) represent possible locations ectopically installed by a bacterial 6 mA methyltransferase, EcoGII. Intervening sequence within chromosomes 5 and 6 is represented as “ . . . ”.

[0054] FIG. 5C shows native polyacrylamide gel analysis and anti-6 mA dot blot analysis of building blocks and purified synthetic chromosomes.

[0055] FIGS. 6A-6E show quantitative modulation of nucleosome occupancy by 6 mA.

[0056] FIG. 6A shows the experimental workflow. Chromatin is assembled using either salt dialysis or the NAP1 histone chaperone. Italicized blue steps are selectively included.

[0057] FIG. 6B shows the tiling qPCR analysis of synthetic chromosome with cognate 6 mA sites. Horizontal gray box represents annotated gene, and vertical black lines depict native 6 mA positions. Horizontal blue bars span −100 bp regions amplified by qPCR. Red horizontal lines represent the region containing 6 mA. Hemi methyl chromosomes contain 6 mA on the antisense and sense strands, respectively, while the Full methyl chromosome has 6 mA on both strands. Black arrowheads: decrease in nucleosome occupancy specifically at the 6 mA cluster.

[0058] FIG. 6C shows the tiling qPCR analysis of ectopically methylated synthetic chromosome. Vertical black lines illustrate possible 6 mA sites installed enzymatically. Red arrowheads: decrease in nucleosome occupancy in the ectopically methylated region. Black arrowheads: position of cognate 6 mA sites (not in this construct).

[0059] FIG. 6D shows the tiling qPCR analysis of chromatin from FIG. 6B that is subsequently incubated with ACF and/or ATP. ACF equalizes nucleosome occupancy between the 6 mA cluster and flanking regions in the presence of ATP (black line). Nucleosome occupancy at the methylated region is not restored to the same level as the unmethylated control (black arrowheads).

[0060] FIG. 6E shows that MNase-seq analysis of chromatin is assembled on native gDNA (“+” 6 mA) and mini-genome DNA (“−” 6 mA) using NAP1±ACF and ATP. p values were calculated using a two-sample unequal variance t test.

[0061] FIGS. 7A-7F show effects of 6 mA on gene expression and cell viability in vivo.

[0062] FIG. 7A shows the following: Horizontal axis: the mean RNA-seq counts across all biological replicates from wild-type and mta1 mutant data for each gene. Vertical axis: log 2(fold change) in gene expression (mutant/wild type).

[0063] FIG. 7B shows that upregulated genes tend to be sparsely methylated compared to randomly subsampled genes (gray lines).

[0064] FIG. 7C shows RNA-seq analysis of MTA1 expression during the sexual cycle of Oxytricha. RNA-seq time course data are from Swart et al. (2013). The total duration of the sexual cycle is ˜60 h.

[0065] FIG. 7D shows survival analysis of Oxytricha cells during the sexual cycle. The total cell number at each time point is normalized to 27 h data to obtain the percentage survival. Error bars represent SEM (n=4).

[0066] FIG. 7E is a model illustrating the impact of 6 mA methylation by MTA1c on nucleosome organization and gene expression.

[0067] FIG. 7F shows the comparison of DNA and RNA N6-adenine methyltransferases. Blue denotes catalytic subunit; yellow denotes subunit with predicted DNA or RNA binding domain.

[0068] FIGS. 8A-8B show MS analysis of 6 mA in ciliate DNA.

[0069] FIG. 8A shows that Oxytricha and Tetrahymena genomic DNA were digested into nucleosides using degradase enzyme mix, followed by analysis using reverse-phase HPLC and mass spectrometry. Isotopically labeled dA and 6 mA standards (.sup.15N5-dA and D3-6 mA) were mixed with each sample to allow quantitative measurement of endogenous dA and 6 mA concentrations. MS/MS analysis of labeled dA and 6 mA standards confirmed the mass of the nucleobase. Fluted peaks with expected masses of dA and 6 mA, and with highly similar retention times (RT) to internal standards are detected in Oxytricha and Tetrahymena nucleosides.

[0070] FIG. 8B shows the quantitation of dA and 6 mA levels in Oxytricha and Tetrahymena gDNA using internal isotopically labeled nucleoside standards. The detected level of 6 mA in Tetrahymena gDNA agrees with earlier reports (Gorovsky et al., 1973; Pratt and Hallman, 1981). The calculated abundance of 6 mA relative to (dA+6 mA) in Oxytricha is ˜0.71%, which is similar to the estimate from SMRT-seq base calls (0.78-1.04%). Note that the calculation from SMRT-seq data is expected to be an overestimate because 6 mA is scored at being present or absent at each site in the genome for this purpose. In actual fact, 6 mA sites may be partially methylated (FIG. 11A). Neither 6 mA nor dA was detected from LC-MS analysis of Oxytricha culture media, arguing against spurious signal arising from contamination or overall technical handling. The PacBio and LC-MS measurements of % 6 mA in Oxytricha are both similar to thin layer chromatography analysis of nucleotides (0.6-0.7%) from a distinct but closely related species, Oxytricha fallax (Rae and Spear, 1978).

[0071] FIGS. 9A-9K show analysis of 6 mA and methyltransferase components in Tetrahymena.

[0072] FIG. 9A shows Tetrahymena MNase-seq data from (Beh et al., 2015), while SMRT-seq data were generated in the present disclosure. Meta-chromosome plots overlaying in vivo MNase-seq (nucleosome occupancy) and SMRT-seq (6 mA), relative to annotated transcription start sites. 6 mA lies mainly within nucleosome linker regions, between the +1, +2, +3, and +4 nucleosomes.

[0073] FIG. 9B shows histograms of the total number of 6 mA marks within each linker in Tetrahymena genes. Calculations are performed as described in FIG. 1B. Distinct linkers are highlighted with horizontal bold blue lines.

[0074] FIG. 9C shows the relationship between transcriptional activity and total number of 6 mA marks in Tetrahymena genes. Analysis is performed as in FIG. 1C. RNA-seq data was obtained from (Xiong et al., 2012).

[0075] FIG. 9D shows that composite analysis of 441,618 methylation sites reveals that 6 mA occurs within a 5′-ApT-3′ dinucleotide motif in Tetrahymena, consistent with previous experiments (Bromberg et al., 1982; Wang et al., 2017) and similar to Oxytricha.

[0076] FIG. 9E shows distribution of various 6 mA dinucleotide motifs across the genome.

[0077] FIG. 9F shows organization of transcription (mRNA-seq), nucleosome organization (MNase-seq), and 6 mA (SMRT-seq) in a Tetrahymena gene.

[0078] FIG. 9G shows that all sequences used for phylogeny construction are listed in Table 1. Abbreviations: Cel: Caenorhabditis elegans; Ath: Arabidopsis thaliana; Sra: Syncephalastrum racemosum; Hve: Hesseltinella vesiculosa; Are: Absidia repens; Dre: Danio redo; Has: Homo sapiens; Ssc: Sus scrota; Mmu: Mus musculus; Xla: Xenopus laevis; Dme: Drosophila melanogaster; Cre: Chlamydomonas reinhardtii; Ltr: Lobosporangium transversale; Lpe: Linderina pennispora; Bme: Basidiobolus meristosporus; Pfi: Piromyces finnis; Aro: Anaeromyces robustus; Tth: Tetrahymena thermophila; Otri: Oxytricha trifallax. This Bayesian phylogenetic tree of MT-A70 proteins is the same as in FIG. 2A, except that all sequences are now included and labeled. TAMT-1 proteins are named according to (Luo et al., 2018).

[0079] FIG. 9H shows Bayesian phylogenetic tree of p1 proteins.

[0080] FIG. 9I shows Bayesian phylogenetic tree of p2 proteins. Dashed box depicts outgroup consisting of vertebrate SNAPC4 genes. These genes bear weak similarity to the homeobox-like domain of p2 proteins, but do not group phylogenetically with them and are therefore unlikely to be functionally homologs.

[0081] FIG. 9J shows phylogenetic distribution of ApT 6 mA motif and various proteins, as depicted in FIG. 2B, but now also including TAMT-1, p1, and p2 proteins. Filled boxes denote the presence of a particular protein in a taxon. Open dashed boxes indicate the presence of SNAPC4 genes in vertebrates.

[0082] FIG. 9K shows the gene expression profiles of Tetrahymena MTA1, MTA9, p1 and p2. Microarray counts represent poly(A)′ expression levels, and are obtained from TetraFGD (Miao et al., 2009; Xiong et al., 2011). MTA1, MTA9, p1 and p2 were found in our study to co-elute with 6 mA methylase activity. On the other hand, TAMT-1 is a putative DNA methyltransferase described by (Luo et al., 2018). The horizontal axis categories beginning with “S” and “C” represent the number of hours since the onset of starvation and conjugation (mating), respectively. “Low,” “Med,” and “High” denote relative cell densities during log-phase growth. Blue and orange traces represent data from two biological replicates. Green and red shaded regions show the peaks in poly(A)* RNA expression in vegetative growth and conjugation, respectively, for MTA1, MTA9, p1 and p2. Note that their expression pattern differs from TAMT-1.

[0083] FIGS. 10A-10N show further characterization of 6 mA methyltransferase activity and MTA1c.

[0084] FIG. 10A shows that fractionation of nuclear extracts on a Q Sepharose column results in two distinct peaks of DNA methyltransferase activity, denoted as “Low Salt sample” and “High Salt sample” by black horizontal bars. FT denotes column flow-through. The DNA methyltransferase assay is performed as in FIG. 2E. The salt concentration at which individual fractions elute from the column is plotted against DNA methyltransferase activity of each fraction (counts per minute). Inset shows DNA methyltransferase activity of the input nuclear extract, flowthrough from the Q Sepharose column, and blank control (nuclear extract buffer). Orange and blue plots denote replicates derived from independent preparations of nuclear extract.

[0085] FIG. 10B is DNA methyltransferase assay showing that the activity from nuclear extracts is heat-sensitive and requires addition of DNA and SAM. Error bars represent s.e.m. (n=3).

[0086] FIG. 10C is dot blot showing that nuclear extracts mediate 6 mA methylation. Note that the low salt sample has substantial DNase activity, resulting in a lower amount of DNA available for dot blot analysis. DNA substrate, nuclear extract, and SAM cofactor were mixed as in panels A and B. The DNA was subsequently purified and used for dot blot analysis.

[0087] FIG. 10D shows domain organization of Tetrahymena MTA1, MTA9, p1, and p2. Protein domains are predicted using hmmscan on the EMBL-EBI webserver (Finn et al., 2015). “aa” denotes amino acids. Start and end coordinates of each domain are stated below each polypeptide.

[0088] FIG. 10E shows the sequence alignment of human (Hsa) METTL3 with Tetrahymena (Tth) and Oxytricha (Otri) MTA1/MTA9, within the MT-A70 domain. Horizontal black bars underscore the DPPW catalytic motif, and the N549/0550 residues in human METTL3 that interact with the ribose moiety of the SAM cofactor. Note that the DPPW catalytic motif is conserved in MTA1 but not MTA9.

[0089] FIG. 10F shows dot blot analysis of hemimethylated dsDNA substrates. Sense or antisense oligonucleotides were first individually methylated using the EcoGII bacterial 6 mA methyltransferase. Each methylated ssDNA was subsequently purified and annealed with an unmethylated complementary strand to form hemimethylated constructs.

[0090] FIG. 10G shows SDS-PAGE analysis of recombinant proteins. Full length proteins were expressed and purified from E. coli. Bands of expected size are indicated with a black arrowhead.

[0091] FIG. 10H is methyttransferase assay using radiolabeled SAM on DNA and RNA substrates, coupled with gel analysis of nucleic acid integrity. ssRNA and dsRNA were produced by in vitro transcription from the 350 bp dsDNA template using 17 RNA polymerase, and subsequently purified before use in this assay. Methyltransferase activity on equimolar amounts of each substrate was measured after incubation at 37° C. for 6 hr, and depicted as either scintillation counts (Counts per minute), or normalized to the 350 bp dsDNA sample (Relative activity). Only dsDNA, and not dsRNA or ssRNA, was methylated. Activity measurements are represented as scintillation counts (counts per minute). In addition, aliquots from each reaction containing DNA or RNA substrate and recombinant MTA1c (ie. MTA1, MTA7, p1 and p2 proteins) were withdrawn at 0, 1, 2, 3, or 6 hr during the 37° C. incubation, purified using phenol:chloroform extraction and ethanol precipitation, and subsequently analyzed on a non-denaturing agarose gel. Both dsDNA and dsRNA substrates remained intact after 6 hr. The ssRNA migrates more diffusely on a nondenaturing agarose gel, with some decrease in size over time, suggesting partial degradation and/or RNA folding; however, there is no detectable methylation of ssRNA despite a significant presence on the agarose gel after 6 hr at 37° C. It is unlikely that this species is too short to be methylated, since MTA1c can methylate significantly shorter substrates such as 27 bp dsDNA (FIGS. 2G, 10I, 10J, and 10K). Error bars represent s.e.m. (n=3).

[0092] FIG. 10I is DNA methyltransferase assay using radiolabeled SAM, on ssDNA oligonucleotides or annealed dsDNA substrates. All four recombinant MTA1c protein components—MTA1, MTA9, p1, and p2—were included in each sample. Activity measurements are represented as scintillation counts (counts per minute). dsDNA substrates were prepared by annealing ssDNA oligonucleotides, as in FIG. 2G. Sense ssDNA nucleotide sequences are depicted in the 5′ 3′ direction, while antisense ssDNA is depicted as 3′ 5′. Error bars represent s.e.m. (n=3).

[0093] FIG. 10J is control [.sup.3H]SAM assay using hemimethylated dsDNA. Reactions depicted in red represent hemimethylated dsDNA incubated with [3H]SAM in the absence of recombinant MTA1c (MTA1, MTA9, p1, and p2 proteins). These reactions showed no methyltransferase activity, verifying that there is no contaminating EcoGII methyltransferase in hemimethylated dsDNA preparations. Activity measurements are shown as scintillation counts, or as “Relative Activity” (normalized against the sample containing unmethylated DNA substrate, [3H]SAM, and MTA1c protein). Hemimethylated dsDNA substrates in this panel are the same as those used in FIG. 2G. The unmethylated dsDNA substrate used in this panel is the same as the top-most dsDNA substrate in FIG. 2G, with two uninterrupted ApT dinucleotides. Error bars represent s.e.m. (n=3).

[0094] FIG. 10K is DNA methyltransferase assay using radiolabeled SAM, on dsDNA substrates with disrupted ApT dinucleotides. All four recombinant MTA1c protein components—MTA1, MTA9, p1, and p2—were included in each sample. Activity measurements are normalized against the parent dsDNA construct with two uninterrupted ApT dinucleotides (top-most construct in this panel). ApT dinucleotide positions are labeled in bold red. Note that the parent dsDNA construct is identical to that in FIG. 10L. Error bars represent s.e.m. (n=3).

[0095] FIG. 10L is DNA methyitransferase assay using radiolabeled SAM, on dsDNA substrates with shifted ApT dinucleotides. All four recombinant MTA1c protein components—MTA1, MTA9, p1, and p2—were included in each sample. Activity measurements are normalized against the parent dsDNA construct with two uninterrupted ApT dinucleotides (top-most construct in this panel). The parent construct is identical to that in FIG. 10K. ApT dinucleotides are labeled in bold red. The adjacent nucleotides are labeled in bold black to highlight the 4-mer sequence that contains each ApT dinucleotide. Error bars represent s.e.m. (n=3).

[0096] FIG. 10M shows motif frequencies of all 4-mer sequences containing methylated ApT dinucleotides in the Tetrahymena and Oxytricha genomes. A′ denotes 6 mA. The 4-mers TA′TA and CKTT are colored in red and blue, respectively, to highlight their large difference in genomic frequencies.

[0097] FIG. 10N shows motif frequencies of 4-mer sequences—regardless of methylation state—in Tetrahymena and Oxytricha. These were calculated from genomic sequence between the 5′ chromosome end and the +4 nucleosome peak (Oxytricha), or between the TSS and the +4 nucleosome peak (Tetrahymena). Analysis was restricted to these regions in order to serve as “background” frequencies for comparison to A′T methylated 4-mers, which are also mainly found downstream of TSSs. The 4-mers TATA and GATT are colored in red and blue, respectively, to facilitate comparison with methylated TA′TA and CA*TT in panel M.

[0098] FIGS. 11A-11D show supplemental SMRT-seq data analyses.

[0099] FIG. 11A shows the following: Top two panels depict PacBio coverage (horizontal axis) plotted against fractional methylation at each called 6 mA site (vertical axis). Bottom left panel is a histogram of fractional methylation of all 6 mA sites. Bottom right panel is a histogram of IPD ratios of all 6 mA sites. Mutant datasets show significantly lower fractional methylation and IPD ratios at 6 mA sites than wild-type data.

[0100] FIG. 11B shows that wild-type SMRT-seq data are randomly subsampled 15 times, such that the resulting coverage is lower than ‘Mal mutant data. The difference in PacBio coverage between mutant and subsampled wild-type data is calculated for each chromosome, and is collectively represented as an olive boxplot (top panel). This set of calculations is repeated 15 times for each subsampled dataset, resulting in a series of 15 boxplots. The difference in PacBio coverage between mutant and fully sampled wild-type data is represented as a violet boxplot. Separately, the difference in total 6 mA marks per chromosome is calculated for respective datasets, and boxplots are shown in the bottom panel. Mutant datasets consistently yield lower numbers of called 6 mA marks than subsampled wild-type, despite the former having higher coverage than the latter.

[0101] FIG. 11C shows the scatterplot of total number of 6 mA marks per chromosome in wild-type versus mutant data. PacBio cutoffs for calling 6 mA marks are varied as shown. A greater number of 6 mA marks per chromosome are consistently detected in wild-type than mutant data.

[0102] FIG. 11D shows the boxplot of PacBio chromosome coverage in individual wild-type and mutant biological replicates (left panel). Only chromosomes with 100-150× PacBio coverage are shown. The total number of 6 mA marks in each of these chromosomes are plotted in the right panel. Wild-type replicates show consistently higher numbers of 6 mA marks per chromosome than mutant replicates.

[0103] FIGS. 12A-12H show analysis of nucleosome organization and confirmation of ectopic DNA insertion in mta1 mutants. Description of analysis in panels A-G: Nucleosomes are grouped according to their “starting” 6 mA level, defined as the total number of 6 mA marks±200 bp from the nucleosome dyad in wild-type cells (WT). The dyad is assigned to be the peak position of MNase-seq reads. Similarly, linkers are grouped according to their “starting” methylation level, defined as the total number of 6 mA marks between two flanking nucleosome dyads (or between the 5′ chromosome end and the terminal nucleosome) in wild-type cells. Loci with high starting 6 mA have methylation greater than or equal to the 90th percentile of starting 6 mA levels, and show greater changes in methylation between mutant and wild-type cells (FIG. 3D). Those with low starting 6 mA are in the lowest 10th percentile. if 6 mA impacts nucleosome organization in vivo, then loci with high starting 6 mA should show a greater change in nucleosome organization. Possible effects are illustrated in panels A-C. Vertical green lines depict 6 mA marks, while blue and red peaks denote nucleosome occupancy. The plots shown in panels A-C illustrate the idealized result if 6 mA disfavors nucleosomes in vivo. Actual effects are shown in panels D-G. “Wild type” is abbreviated as WT. Analyses are restricted to the 5′ chromosome end.

[0104] FIG. 12A shows that 6 mA loss may result in an increase in nucleosome fuzziness (highlighted with bold red double-sided arrow). The effect should be greater for nucleosomes with high starting 6 mA due to greater change in 6 mA between mutant and wild-type cells (“Change in nucleosome fuzziness” Box). Nucleosomes should, in turn, exhibit lower occupancy near the peak position, and higher occupancy in flanking regions (“Change in Nucleosome occupancy” Box; highlighted with red arrowheads and plotted ±73 bp from the dyad). Nucleosome fuzziness is calculated as the standard deviation of MNase-seq read locations ±73 bp from the dyad.

[0105] FIG. 12B shows that 6 mA loss from nucleosome linker regions may result in a decrease in linker length (highlighted with bold red bracket). If so, the magnitude of decrease in linker length should be greater for linkers with high starting 6 mA (“Change in linker length” Box).

[0106] FIG. 12C shows that 6 mA loss may result in an increase in occupancy directly over the methylated linker region (highlighted with bold red bracket). If so, the magnitude of increase in linker occupancy should be greater for regions with high starting 6 mA (“Change in linker occupancy” Box). Linker occupancy denotes the average MNase-seq coverage ±25 bp from the midpoint between flanking nucleosome dyads or chromosome end. As an example, for the +1/+2 nucleosome linker, occupancy is calculated ±25 bp from the midpoint of the +1 and +2 nucleosome dyad positions. Since nucleosome linker length in Oxytricha is ˜200 bp (FIG. 12F, bottom panels), the genomic window used to calculate linker occupancy has minimal overlap with that for calculating nucleosome fuzziness and occupancy in panel A.

[0107] FIG. 12D shows the impact of 6 mA loss on nucleosome fuzziness. For each nucleosome, the change in fuzziness between mutant and wild-type cells is calculated. Boxplots represent the distribution of changes in fuzziness scores. “MNase-seq” denotes sequencing of nucleosomal DNA obtained from Oxytricha chromatin in vivo, while “Control gDNA-seq” represents sequencing of MNase-digested, naked genomic DNA in vitro. Boxplot features are as described in FIG. 1C. Distributions are compared using a Wilcoxon rank-sum test. N.S denotes “non-significant,” with p>0.01.

[0108] FIG. 12E shows the impact of 6 mA loss on nucleosome occupancy. For each nucleosome, the difference in nucleosome occupancy between mutant and wild-type cells is calculated at individual basepairs±73 bp around the nucleosome dyad. Data are averaged and depicted as line plots. The change in occupancy at the dyad is compared between nucleosomes with high and low starting 6 mA using a Wilcoxon rank-sum test.

[0109] FIG. 12F shows the impact of 6 mA loss on linker length. Three types of linkers are analyzed: between the 5′ chromosome end and +1 nucleosome dyad, between the +1 and +2 nucleosome dyads, and between the +2 and +3 nucleosome dyads. For each linker, the difference in its length between mutant and wild-type cells is calculated. The resulting distribution of linker length differences is plotted as a histogram (top-most row of this panel). Distributions of linker length differences are compared using two-sample unequal variance t test. N.S. indicates “not significant,” with p>0.01. Separately, the respective distributions of linker lengths in mutant and wild-type cells are plotted in the bottom two rows of this panel. The median linker length from each group is included as an inset.

[0110] FIG. 12G shows the impact of 6 mA loss on linker occupancy. Linkers are binned as in panel F. For each linker, the difference in occupancy between mutant and wild-type cells is calculated. The resulting distribution of changes in linker occupancy is represented as a boxplot. Distributions are compared using two-sample unequal variance t test. N.S. indicates “not significant,” with p>0.01. Boxplot features are as described in FIG. 1C.

[0111] FIG. 12H shows poly(A).sup.+ RNaseq analysis of wild-type and mta1 mutants. “ATG” denotes start codon of MTA1 gene. A 62 bp ectopic DNA insertion results in a frameshift mutation in the MTA1 coding region. Three wild-type (WTI, WT2, wr3) and mutant (mta1′, mta12, mta13) biological replicates are analyzed. Short horizontal bars represent RNaseq reads, which are, −.75 nt in length and mapped to the reference sequence. For a read to be successfully mapped, it must have no more than 2 mismatches relative to the reference sequence. Unmapped reads are discarded. Blue and red bars denote RNaseq reads that map to native and ectopic regions, respectively. RNaseq reads overlapping the ectopic region are detected in mutant but not wild-type replicates. These reads span junctions between the ectopic and flanking coding regions, confirming the site of ectopic insertion.

[0112] FIGS. 13A-13I show gel analysis of histone octamers and assembled chromatin. Description for panels A-D: Xenopus unmodified core histones were recombinantly expressed. Oxytricha histones were acid-extracted from vegetative nuclei. Oxytricha and Xenopus histones were subsequently refolded into octamers and purified through size exclusion chromatography. Description for panels E-I: Xenopus or Oxytricha histone octamers were assembled on DNA and subsequently digested with MNase to obtain ˜150 bp mononucleosome-sized fragments (labeled with red arrowheads). The resulting products were visualized by agarose gel electrophoresis. Mononucleosomal DNA was gel-excised and analyzed using Illumina sequencing or tiling qPCR analysis in FIGS. 4A-4E, 6A—6E, and 14A—14F.

[0113] FIG. 13A shows reverse-phase HPLC purification of acid-extracted Oxytricha histones. Fractions 1-5 were individually collected and analyzed by Coomassie staining and western blotting.

[0114] FIG. 13B shows SDS-PAGE analysis of purified Oxytricha histone fractions.

[0115] FIG. 13C shows Western blot analysis of Oxytricha histone fractions 1-5. The fraction that is most enriched in each type of histone is colored in red. Arrowheads indicate likely histone bands.

[0116] FIG. 13D shows SDS-PAGE analysis of purified Oxytricha and Xenopus histone octamers.

[0117] FIG. 13E shows that chromatin was assembled on PCR-amplified Oxytricha mini-genome DNA, digested with MNase, and analyzed by agarose gel electrophoresis.

[0118] FIG. 13F shows that chromatin was assembled on native Oxytricha genomic DNA, digested with MNase, and analyzed by agarose gel electrophoresis.

[0119] FIG. 13G shows that chromatin was assembled with synthetic chromosome DNA, digested with MNase, and visualized by agarose gel electrophoresis. All assemblies with synthetic chromosomes were performed in the presence of an approximately 100-fold mass excess of buffer DNA relative to synthetic chromosome (see Example 1). This applies to panels G, H, and I. Representative assemblies with the unmethylated chromosome are shown. Methylated chromosome assemblies were separately performed in place of the unmethylated variant.

[0120] FIG. 13H shows that chromatin was assembled on unmethylated synthetic chromosomes by salt dialysis and subsequently incubated with ACF and/or ATP. The resulting mixture was digested with MNase and visualized by agarose gel electrophoresis. Regularly spaced nucleosomes (labeled with red dots) are observed only when chromatin was incubated with both ACF and ATP.

[0121] FIG. 13I shows chromatin assembled on unmethylated synthetic chromosomes using the NAP1 histone chaperone in the presence of ACF and/or ATP. The resulting mixture was digested with MNase and visualized by agarose gel electrophoresis. Nucleosomes are regularly spaced (labeled with red dots) in the presence of both ACF and ATP, although less apparent than in panel H.

[0122] FIGS. 14A-14F show control MNase-Seq and tiling qPCR analysis.

[0123] FIG. 14A is the same analysis as FIG. 4C, showing that 6 mA quantitatively disfavors nucleosome occupancy in vitro but not in vivo. Here, the extent of MNase digestion was 40% of that in FIG. 4C. P-values were calculated using a two-sample unequal variance t test. N.S denotes “non-significant,” with p>0.05.

[0124] FIG. 14B is the same analysis as FIG. 6E, showing that the ACF complex restores nucleosome occupancy over methylated DNA in an ATP-dependent manner in vitro. Here, the extent of MNase digestion was 25% of that in FIG. 6E. P-values were calculated using a two-sample unequal variance t test. N.S denotes “non-significant,” with p>0.05.

[0125] FIG. 14C is the same analysis as FIG. 12D, showing that nucleosomes with high starting 6 mA show larger changes in fuzziness. Here, the extent of MNase digestion was 40% of that in FIG. 12D. Distributions are compared using a Wilcoxon rank-sum test. N.S denotes “non-significant,” with p>0.01.

[0126] FIG. 14D is the same analysis as FIG. 12E, showing that nucleosomes with high starting 6 mA exhibit characteristic changes in nucleosome occupancy at and around the nucleosome dyad. Here, the extent of MNase digestion was 40% of that in FIG. 12E. The change in dyad occupancy is compared between nucleosomes with high and low starting 6 mA using a Wilcoxon rank-sum test. N.S denotes “non-significant,” with p>0.01.

[0127] FIG. 14E shows tiling qPCR analysis of nucleosome occupancy in spike-in and homogeneous synthetic chromosome preparations. The blunt, unmethylated synthetic chromosome (construct #1 in FIG. 5B) was used for chromatin assembly with (“Spike-in”) or without (“Homogeneous”) a 100-fold excess of buffer DNA. In the latter case, an equivalent mass of synthetic chromosome was added in place of buffer DNA to maintain the same DNA concentration for chromatin assembly. The tiling qPCR assay was performed as in FIG. 6B. Shaded red bars depict the regions where 6 mA modulates nucleosome occupancy in separate methylated chromosomes analyzed in FIGS. 6B and 6C. Note that methylated chromosomes were not used to generate qPCR data for this figure. Black arrowheads indicate no decrease in nucleosome occupancy in these regions when buffer DNA is used. Thus, the decrease in nucleosome occupancy in methylated chromosomes reported in FIGS. 6A-6E cannot be attributed to spike-in versus homogeneous addition of DNA for chromatin assembly. Error bars in all panels represent s.e.m. (n=3-4).

[0128] FIG. 14F shows that chromatin was assembled on synthetic chromosomes using the NAP1 histone chaperone in the presence of ACF and/or ATP, instead of set dialysis. qPCR analysis was performed as in FIG. 6B. Methylated chromosomes used in this experiment contain 6 mA in native sites. The addition of ACF and ATP results in a partial restoration of nucleosome occupancy over the methylated region. These results are similar to FIG. 6D, where chromatin was assembled by sat dialysis instead of NAP1.

[0129] FIG. 15 shows that ciliate methyltransferase MTA1c mediates DNA N6-adenine methylation (6 mA) in vivo and 6 mA directly disfavors nucleosome occupancy in vitro.

DETAILED DESCRIPTION OF THE DISCLOSURE

[0130] DNA N6-adenine methylation (6 mA) has recently been described in diverse eukaryotes, spanning unicellular organisms to metazoa. In the present disclosure, it's reported a DNA 6 mA methyltransferase complex in ciliates, termed MTA1c. It consists of two MT-A70 proteins and two homeobox-like DNA-binding proteins and specifically methylates dsDNA. Disruption of the catalytic subunit, MTA1, in the ciliate Oxytricha leads to genome-wide loss of 6 mA and abolishment of the consensus ApT dimethylated motif. Mutants fail to complete the sexual cycle, which normally coincides with peak MTA1 expression. The present disclosure investigates the impact of 6 mA on nucleosome occupancy in vitro by reconstructing complete, full-length Oxytricha chromosomes harboring 6 mA in native or ectopic positions. It's shown that 6 mA directly disfavors nucleosomes in vitro in a local, quantitative manner, independent of DNA sequence. Furthermore, the chromatin remodeler ACF can overcome this effect. The present disclosure identifies a diverged DNA N6-adenine methyltransferase and defines the role of 6 mA in chromatin organization.

[0131] One embodiment of the present disclosure is a method of modifying a nucleic acid from a cell, the cell derived from a multicellular eukaryote. This method comprises the steps of: (a) obtaining the nucleic acid from the cell; and (b) contacting the nucleic acid with MTA1c or any components thereof under conditions effective to methylate the nucleic acid.

[0132] In some embodiments, the nucleic acid is RNA or DNA. In some embodiments, the eukaryotic cell is mammalian. In some embodiments, the multicellular eukaryote is a human. In some embodiments, the modification is a DNA N6-adenine methylation including one of more of the following motifs: dimethylated AT (5′-A*T-3′/3′-TA*-5′), dim ethylated TA (5′-TA*-3′/3′-A*T-5′), dim ethylated AA (5′-A*A*-3′/3′-TT-5′), methylated AT (5′-A*T-3′/3′-TA-5′), methylated AA (5′-A*A-3′/3′-TT-5′), methylated AC (5′-A*C-3′/3′-TG-5′), methylated AG (5′-A*G-3′/3′-TC-5′), methylated TA (5′-TA*-3′/3′-AT-5′), methylated AA (5′-AA*-3′/3′-TT-5′), methylated CA (5′-CA*-3′/3′-GT-5′), and methylated GA (5′-GA*-3′/3′-CT-5′). In certain embodiments, the MTA1 or an ortholog thereof comprises a mutation effective to abrogate dimethylation of the nucleic acid. Preferably, the mutation comprises loss of a C-terminal methyltransferase domain. In some embodiments, the MTA1c or any components thereof is obtained from ciliates, algae, or basal fungi. Preferably, the MTA1c or any components thereof is obtained from Oxytricha or Tetrahymena.

[0133] As used herein, an “ortholog,” or orthologous gene, is a gene with a sequence that has a portion with similarity to a portion of the sequence of a known gene, but found in a different species than the known gene. An ortholog and the known gene originated by vertical descent from a single gene of a common ancestor. As used herein an ortholog encodes a protein that has a portion of at least about 50%, such as at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80% or at least about 80% of the total length of the sequence of the encoded protein that is similar to a portion of a length of at least about 50%, such as at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80% or at least about 80% of a known protein. The respective portion of the ortholog and the respective portion of the known protein to which it is similar may be a continuous sequence or be fragmented a number, for example, into 1 to about 3, including 2, individual regions within the sequence of the respective protein. For example, the 1 to about 3 regions are arranged in the same order in the amino acid sequence of the ortholog and the amino acid sequence of the known protein. Such a portion of an ortholog has an amino acid sequence that has at least about 40%, at least about 45%, such as at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75% or at least about 80% sequence identity to the amino acid sequence of the known protein encoded by a MTA1 gene.

[0134] As used herein, an asterisk “*” indicates the presence of a methylated base. For example, “A*” represents a methylated adenine.

[0135] The modified base, m6dA, has been discovered in a wide range of eukaryotes, including humans. m6dA levels are significantly reduced in gastric and liver cancer tissues, and disruption of m6dA promotes tumor formation (Xiao et al. 2018). As disclosed herein, MTA1 is a novel m6dA “writer”, paving the way for cost-effective methods to understand mechanisms of m6dA function in biomedically relevant models.

[0136] Accordingly, another embodiment of the present disclosure is a method of treating or ameliorating the effects of a disease characterized by an abnormal level of m6dA in a subject. This method comprises administering to the subject an amount of MTA1c or any components thereof effective to modulate m6dA levels in the subject. In some embodiments, the modulation comprises restoring m6dA levels to normal or near-normal ranges in the subject.

[0137] In some embodiments, the subject is a mammal that can be selected from the group consisting of humans, veterinary animals, and agricultural animals. Preferably, the subject is a human.

[0138] In some embodiments, the disease is a cancer, e.g., gastric cancer or liver cancer. In certain embodiments, the method further comprises administering to the subject one or more of anti-gastric cancer and anti-liver cancer drugs. Non-limiting examples of anti-liver cancer drugs include Nexavar™ (Sorafenib Tosylate) and Stivarga™ (Regorafenib). Non-limiting examples of anti-gastric cancer drugs include Cyramza™ (Ramucirumab), Doxorubicin Hydrochloride, 5-FU (Fluorouracil Injection), Fluorouracil Injection, Herceptin™ (Trastuzumab), Mitomycin C, Taxotere™ (Docetaxel), Trastuzumab, Afinitor™ (Everolimus), Somatuline Depot™ (Lanreotide Acetate), FU-LV, TPF, and XELIRI.

[0139] In some embodiments, the method furthering comprises co-administering to the subject an epigenetic agent that is selected from the group consisting of methylation inhibiting drugs, Bromodomain inhibitors, histone acetylase (HAT) inhibitors, protein methyltransferase inhibitors, histone methylation inhibitors, histone deacetlyase (HDAC) inhibitors, histone acetylases, histone deacetlyases, and combinations thereof.

[0140] Another embodiment of the present disclosure is a pharmaceutical composition comprising MTA1c or any components thereof that is effective to modulate m6dA levels in a subject in need thereof and a pharmaceutically acceptable carrier, diluent, adjuvant or vehicle.

[0141] Yet another embodiment of the present disclosure is a kit for treating or ameliorating the effects of a disease characterized by an abnormal level of m6dA in a subject, such as, e.g., cancer, comprising an effective amount of MTA1c or any components thereof, packaged together with instructions for its use.

[0142] Another embodiment of the present disclosure is a cell line obtained from a multicellular eukaryote comprising a nucleic acid encoding MTA1c or any components thereof and/or an MTA1c protein complex or any components thereof. As used herein, a “cell line” refers to all types of cell lines such as, e.g., immortalized cell lines and primary cell lines. In certain embodiments, the nucleic acid encoding MTA1c or any components thereof is operably linked to a recombinant expression vector.

[0143] Another embodiment of the present disclosure is a recombinant expression vector comprising a polynucleotide encoding MTA1c or any components thereof.

[0144] Still another embodiment of the present disclosure is a transgenic organism whose genome comprises a transgene comprising a nucleotide sequence encoding MTA1c or any components thereof. Non-limiting examples of possible organism include an archaea, a bacterium, a eukaryotic single-cell organism, algae, a plant, an animal, an invertebrate, a fly, a worm, a cnidarian, a vertebrate, a fish, a frog, a bird, a mammal, an ungulate, a rodent, a rat, a mouse, and a non-human primate.

[0145] The present disclosure also provides a method of identifying protein binding sites on DNA. This method comprises the steps of: (a) providing DNA; (b) contacting the DNA with MTA1c or any components thereof under conditions effective to methylate the DNA; (c) contacting the DNA with one or more proteins; (d) contacting the DNA with an enzyme effective to hydrolize the DNA in positions where no protein binding occurs; (e) removing the DNA bound protein; and (f) isolating and sequencing the DNA fragments. In certain embodiments, the one or more proteins in step (c) comprise histone octamers.

[0146] Another embodiment of the present disclosure is a method of mediating DNA N6-adenine methylation. This method comprises the steps of: (a) providing DNA; and (b) contacting the DNA with MTA1c or any components thereof under conditions effective to methylate the DNA.

[0147] Another embodiment of the present disclosure is a method of modulating nucleosome organization and/or transcription in a cell, comprising providing to the cell an agent that is effective to modulate the expression of MTA1c or any components thereof.

[0148] The present disclosure also provides a method of generating a synthetic chromosome. This method comprises the steps of: (a) generating chromosome segments containing terminal restriction sites, wherein the chromosome segments comprise one or more m6dA bases; (b) digesting the chromosome segments with a restriction enzyme; and (c) purifying and ligating the digested chromosome segments to form a synthetic chromosome. In some embodiments, the method further comprises enriching the synthetic chromosome. A synthetic chromosome made by the method above is also provided.

[0149] The following examples are provided to further illustrate certain aspects of the present disclosure. These examples are illustrative only and are not intended to limit the scope of the disclosure in any way.

EXAMPLES

Example 1

Materials and Methods

[0150]

TABLE-US-00001 KEY RESOURCES TABLE REACIENT or RESOURCE SOURCE IDENTIFIER Antibodies Anti-H2A Active Motif Cat #: 39111 Anti-H2B Abcam Cat #: 1790 Anti-H3 Abcam Cat #: 1791 Anti-H4 Active Motif Cat #: 39269 Anti-N6-methyladenosine Cedarlane Cat #: 202003(SY) antibody Labs/Synaptic Systems Goat Anti-Rabbit IgG Bio-Rad 1706515 (H + L)-HRP Conjugate Bacterial and Virus Strains One Shot TOP10 chemically Thermo Fisher Cat #: C404006 competent E. coli BL21(DE3) pLysS Thermo Fisher Cat #: 70-236-4 SHuffle T7 Express NEB Cat #: C3029J Competent E. coli Lemo21 (DE3) Competent NEB Cat #: C2S28J E. coli Chemicals, Peptides, and Recombinant Proteins Micrococcal nuclease NEB Cat #: M0247S Q5 Site-Directed NEB Cat #: E0554S Mutagenesis Kit ProBlock Gold bacterial GoldBio Cat #: GB-330-5 protease inhibitor cocktail Proteinase K Roche Cat #: 3113879001 Phenol:Chloroform:IAA, Thermo Fisher Cat #: AM9732 25:24:1 TRIzol reagent Thermo Fisher Cat #: 15596026 DNA Polymerase I, Large NEB Cat #: M0210S (Klenow) Fragment Klenow Fragment NEB Cat #: M0212S (3′ .fwdarw. 5′ exo-) Bsal NEB Cat #: R3535S EcoGII NEB Cat #: M0603S T4 DNA ligase NEB Cat #: M0202M Phusion DNA polymerase NEB Cat #: M0530L S-adenosyl-L-methionine NEB Cat #: B9003S Mouse NAP1 This study N/A Drosophila ACF complex Active Motif Cat #: 31509 Xenopus histones This study N/A Polyvinyl alcohol Sigma Aldrich Cat #: P8136 Polyethylene glycol 8000 Sigma Aldrich Cat #: P2139 Adenosine Sigma Aldrich Cat #: A6559-25UMO 5′-triphosphate (ATP) Creatine phosphate Sigma Aldrich Cat #: 10621714001 Creatine kinase Sigma Aldrich Cat #: 10127566001 Power SYBR Green PCR master Thermo Fisher Cat #: 4367659 mix Gum Arabic Sigma Aldrich Cat #: G9752-1KG 3H-labeled PerkinElmer Cat #: NET155V250UC S-adenosyl-L-methionine ([3H]SAM) Ultima Gold PerkinElmer Cat #: 6013326 DNA degradase plus enzyme Zymo Research Cat #: E2020 .sup.15N.sub.5-dA nucleoside Cambridge Cat #: NLM-3895-25 Isotope Laboratories D.sub.3-6mA Synthesized N/A in this study Critical Commercial Assays QIAquick gel extraction kit QIAGEN Cat #: 28706 NEBNext Poly(A) mRNA NEB Cat #: E7490S Magnetic Isolation Module ScriptSeq v2 RNA-Seq Illumina Cat #: SSV21124 Library Prep Kit Nucleospin Tissue Kit Takara Bio Cat #: 740952.250 USA MinElute Reaction Cleanup QIAGEN Cat #: 28206 Kit NEBNext Ultra II DNA NEB Cat #: E7645S Library Prep Kit Hi-Scribe T7 High Yield NEB Cat #: E2040S RNA Synthesis Kit Dynabeads Protein A Thermo Fisher Cat #: 10001D TOPO TA cloning kit Thermo Fisher Cat #: K457501 Deposited Data Oxytricha trifallax This study SRA: SRX2335608 and SMRT-seq SRX2335607 Tetrahymena thermophila This study GEO: GSE94421 SMRT-seq Oxytricha trifallax, all This study GEO: GSE94421 Illumina data (RNA- seq, 6mA-IP-seq, MNase-seq, gDNA-seq) Experimental Models: Organisms/Strains Oxytricha trifallax cells, Lab collection N/A strain JRB310 Oxytricha trifallax cells, Lab collection N/A strain JRB510 Oxytricha trifallax cells, Lab collection N/A mtal mutant Tetrahymena thermophila Tetrahymena Cat #: SD00703 cells, strain SB210 stock center Oligonucleotides All are listed in Table S4 IDT N/A Recombinant DNA pET-His-NAP1 (expression This study N/A vector for recombinant NAP1) pET-XenH2A (expression This study N/A vector for recombinant Xenopus histone H2A) pET-XenH2B (expression This study N/A vector for recombinant Xenopus histone H2B) pET-XenH3 (expression This study N/A vector for recombinant Xenopus histone H3) pET-XenH4 (expression This study N/A vector for recombinant Xenopus histone H4) pET-HisSUMO-MTA1 This study N/A (expression vector for recombinant Tetrahymena MTA1) pET-HisSUMO-MTA7 This study N/A (expression vector for recombinant Tetrahymena MTA7) pET-HisSUMO-p1 This study N/A (expression vector for recombinant Tetrahymena p1) pET-HisSUMO-p2 This study N/A (expression vector for recombinant Tetrahymena p2) pCR-TOPO- This study N/A syntheticChromosome (cloned synthetic chromosomes to verify accuracy of ligation of component DNA building blocks) Software and Algorithms Galaxy Galaxy https://usegalaxy.org/ Community Hub Bowtie2 Langmead and http://bowtie-bio.sourceforge.net/bowtie2/index.shtml Salzberg, 2012 TopHat2 TopHat2 https://ccb.jhu.edu/software/tophat/index.shtml (Mortazavi et al., 2008) Python 2.7.10 Python Software https://www.python.org/download/releases/2.7/ Foundation CAGEr Haberle et https://bioconductor.org/packages/release/bioc/html/CAGEr.html al.. 2015 SMRT Analysis 2.3.0 Pacific https://www.pacb.com/documentation/smrt-analysis-software-installation-v2-3-0/ Biosciences PSI-BLAST NCBI/NIH https://blast.ncbi.nlm.nih.gov/ Blast.cgi?CMD=Web&PAGE-Proteins&PROGRAM-blastp&RUN_PSIBLAST=on CD-HIT Huang et al., http://weizhong-lab.ucsd.edu/cdhit-web-server/cgi-bin/index.cgi 2010 MAFFT Katoh et al., https://mafft.cbrc.jp/alignment/software/ 2017; Kuraku et al., 2013 MrBayes/CIPRES Science Miller et al., https://www.phylo.org/ Gateway 2010 R (v3.2.5) The R Foundation https://www.r-project.org/ hmmscan Finn et al., https://www.ebi.ac.uk/Tools/hmmer/search/hmmscan 2015 Other Agencourt Ampure XP beads Beckman Coulter Cat #: A63880 Acid-extracted Oxytricha This study N/A histones Slide-A-Lyzer 3.5K MWCO Thermo Fisher Cat #: PI66110 cassette Amersham Hybond-XL membrane GE Healthcare Cat #: RPN303S Amersham Hybond-N+ GE Healthcare Cat #: RPN119B membrane Volvic water Amazon https://www.amazon.com/Volvic-500m1-6-Pack/dp/B013PCK8M4/ ref=sr_1_1_a_it?_ie=UTF8&qid=1538873999&sr=8- 1&keyword_s=volvic&dpID=418qEyu6yrUpreST=_SY300 QL70 &dpSrc=srch
Oxytricha trifallax

[0151] Vegetative Oxytricha trifallax strain J RB310 was cultured at a density of 1.5×10.sup.7 cells/L to 2.5×10.sup.7 cells/L in Pringsheim media (0.11 mM Na.sub.2HPO.sub.4, 0.08 mM MgSO.sub.4, 0.85 mM Ca(NO.sub.3).sub.2, 0.35 mM KCl, pH 7.0) and fed daily with Chlamydomonas reinhardtii. Cells were filtered through cheesecloth to remove debris and collected on a 10 pm Nitex mesh for subsequent experiments.

Tetrahymena thermophila

[0152] Stock cultures of vegetative Tetrahymena thermophila strain SB210 were maintained in Neff medium (0.25% w/v proteose peptone, 0.25% w/v yeast extract, 0.5% glucose, 33.3 pM FeCl.sub.3). These cultures were inoculated into SSP medium (2% w/v proteose peptone, 0.1% w/v yeast extract, 0.2% w/v glucose, 33 pM FeCl.sub.3) and grown to log-phase (˜3.5×10.sup.5 cells/mL) through constant shaking at 125 rpm/30° C.

In Vivo MNase-Seq

[0153] 3×10.sup.5 vegetative Oxytricha cells were fixed in 1% w/v formaldehyde for 10 min at room temperature with gentle shaking, and then quenched with 125 mM glycine. Cells were lysed by dounce homogenization in lysis buffer (20 mM Tris pH 6.8, 3% w/v sucrose, 0.2% v/v Triton X-100, 0.01% w/v spermidine trihydrochloride) and centrifuged in a 10%-40% discontinuous sucrose gradient (Lauth et al., 1976) to purify macronuclei. The resulting macronuclear preparation was pelleted by centrifugation at 4000×g, washed in 50 ml TMS buffer (10 mM Tris pH 7.5, 10 mM MgCl.sub.2, 3 mM CaCl.sub.2), 0.25M sucrose), resuspended in a final volume of 300 μL, and equilibriated at 37° C. for 5 min. Chromatin was then digested with MNase (New England Biolabs) at a final concentration of 15.7 Kunitz Units/μL at 37° C. for 1 min 15 s, 3 min, 5 min, 7 min 30 sec, 10 min 30 s, and 15 min respectively. Reactions were stopped by adding ½ volume of PK buffer (300 mM NaCl, 30 mM Tris pH 8, 75 mM EDTA pH 8, 1.5% w/v SDS, 0.5 mg/mL Proteinase K). Each sample was incubated at 65° C. overnight to reverse crosslinks and deproteinate samples. Subsequently, nucleosomal DNA was purified through phenol:chloroform:isoamyl alcohol extraction and ethanol precipitation. Each sample was loaded on a 2% agarose-TAE gel to check the extent of MNase digestion. The sample exhibiting −80% mononucleosomal species was selected for MNase-seq analysis, in accordance with previous guidelines (Zhang and Pugh, 2011). Mononucleosome-sized DNA was gel-purified using a QIAquick gel extraction kit (QIAGEN). Illumina libraries were prepared using an NEBNext Ultra II DNA Library Prep Kit (New England Biolabs) and subjected to paired-end sequencing on an Illumina HiSeq 2500 according to manufacturer's instructions. All vecietative Tetrahymena MNase-sea data were obtained from (Beh et al., 2015).

Poly(A).SUP.+ RNA-Seq and TSS Sequencing

[0154] Oxytricha cells were lysed in TRIzol reagent (Thermo Fisher Scientific) for total RNA isolation according to manufacturer's instructions. Poly(A).sup.+ RNA was then purified using the NEBNext Poly(A) mRNA Magnetic Isolation Module (New England Biolabs). Oxytricha poly(A).sup.+ RNA was prepared for RNA-seq using the ScriptSeq v2 RNA-Seq Library Preparation Kit (Illumina). Tetrahymena poly(A).sup.+ RNA-seq data was obtained from (Xiong et al., 2012). The 5′ ends of capped RNAs were enriched from vegetative Oxytricha total RNA using the RAMPAGE protocol (Batut et al., 2013), and used for library preparation, Illumina sequencing and subsequent transcription start site determination (ie. “TSS-seq”). These data were used to plot the distribution of Oxytricha TSS positions in FIG. 1A. TSS positions used for analysis outside of FIG. 1A were obtained from (Swart et al., 2013) and (Beh et al., 2015). For RNaseq analysis of genes grouped according to “starting” methylation level level: total 6 mA was counted between 100 bp upstream to 250 bp downstream of the TSS. Genes with high starting methylation have total 6 mA in the 90th percentile and higher. Genes with low starting methylation have total 6 mA at or below the 10th percentile.

Immunoprecipitation and Illumina Sequencing of Methylated DNA (6 mA IP-Seq)

[0155] Genomic DNA was isolated from vegetative Oxytricha cells using the Nucleospin Tissue Kit (Takara Bio USA, Inc.). DNA was sheared into 150 bp fragments using a Covaris LE220 ultra-sonicator (Covaris). Samples were gel-purified on a 2% agarose-TAE gel, blunted with DNA polymerase I (New England Biolabs), and purified using MinElute spin columns (QIAGEN). The fragmented DNA was dA-tailed using Klenow Fragment (3′->5′ exo-) (New England Biolabs) and ligated to Illumina adaptors following manufacturer's instructions. Subsequently, 2.2 μg of adaptor-ligated DNA containing 6 mA was immunoprecipitated using an anti-N6-methyladenosine antibody (Cedarlane Labs) conjugated to Dynabeads Protein A (Invitrogen). The anti-6 mA antibody is commonly used for RNA applications, but has also been demonstrated to recognize 6 mA in DNA (Fioravanti et al., 2013; Xiao and Moore, 2011). The immunoprecipitated and input libraries were treated with proteinase K, extracted with phenol:chloroform, and ethanol precipitated. Finally, they were PCR-amplified using Phusion Hot Start polymerase (New England Biolabs) and used for Illumina sequencing.

Sample Preparation for SMRT-Seq

[0156] Vegetative Oxytricha macronuclei were isolated as described in the subheading “in vivo MNase-seq” of this study. Vegetative Tetrahymena macronuclei were isolated by differential centrifugation (Beh et al., 2015). Oxytricha and Tetrahymena cells were not fixed prior to nuclear isolation. Genomic DNA was isolated from Oxytricha and Tetrahymena macronuclei using the Nucleospin Tissue Kit (Macherey-Nagel). Alternatively, whole Oxytricha cells instead of macronuclei were used. SMRT-seq according to manufacturer's instructions, using P5-C3 and P6-C4 chemistry, as in (Chen et al., 2014). Oxytricha and Tetrahymena macronuclear DNA were used for SMRT-seq in FIGS. 1A-1E and 9A-9F, while Oxytricha whole cell DNA was used for all other Figures. Since almost all DNA in Oxytricha cells is derived from the macronucleus (Prescott, 1994), similar results are expected between the use of purified macronuclei or whole cells.

Illumina Data Processing

[0157] Reads from all biological replicates were merged before downstream processing. All Illumina sequencing data were quality trimmed (minimum quality score=20) and length-filtered (minimum read length=40nt) using Galaxy (Blankenberg et al., 2010; Giardine et al., 2005; Goecks et al., 2010). MNase-seq and 6 mA IP-seq reads were mapped to complete chromosomes in the Oxytricha trifallax JRB310 (August 2013 build) or Tetrahymena thermophila SB210 macronuclear reference genomes (June 2014 build) using Bowtie2 (Langmead and Salzberg, 2012) with default settings, while poly(A). RNA-seq and TSS-seq reads were mapped using TopHat2 (Mortazavi et al., 2008) with August 2013 Oxytricha gene models or June 2014 Tetrahymena gene models, with default settings.

[0158] MNase-seq datasets were generated by paired-end sequencing. Within each MNase-seq dataset, the read pair length of highest frequency was identified. All read pairs with length±25 bp from this maximum were used for downstream analysis. On the other hand, 6 mA IP-seq datasets were generated by single-read sequencing. 6 mA IP-seq single-end reads were extended to the mean fragment size, computed using cross-correlation analysis (Kharchenko et al., 2008). The per-basepair coverage of Oxytricha MNase-seq read pair centers and extended 6 mA IP-seq reads were respectively computed across the genome. Subsequently, the per-basepair coverage values were normalized by the average coverage within each chromosome to account for differences in DNA copy number (and hence, read depth) between Oxytricha chromosomes (Swart et al., 2013). The per-basepair coverage values were then smoothed using a Gaussian filter of standard deviation=15. This smoothed data is denoted as “normalized coverage” or “nucleosome occupancy.” Tetrahymena MNase-seq data were processed similarly to Oxytricha, except that DNA copy number normalization was omitted as Tetrahymena chromosomes have uniform copy number (Eisen et al., 2006).

[0159] For the MNase-seq analysis in FIGS. 4C, 6E, 14A, and 14B, nucleosome occupancy and 6 mA IP-seq coverage were calculated within overlapping 51 bp windows across the 98 assayed chromosomes. Windows were binned according to the number of 6 mA residues within. The in vitro MNase-seq coverage from chromatinized native gDNA (“+” 6 mA) was divided by the corresponding coverage from chromatinized mini-genome DNA (“−” 6 mA) to obtain the fold change in nucleosome occupancy in each window. Alternatively, a subtraction was performed on these datasets to obtain the difference in nucleosome occupancy in vitro. Identical DNA sequences were compared for each calculation. These data are labeled as (“+” histones) in FIGS. 4C and 14A. Naked native gDNA and mini-genome DNA were also MNase-digested, sequenced and analyzed in the same manner to control for Mnase sequence preferences (“−” histones). Nucleosome occupancy in vivo corresponds to normalized MNase-seq coverage from wild type and mta1 mutant cells.

[0160] Nucleosome positions were iteratively called as local maxima in normalized MNase-seq coverage, as previously described (Beh et al., 2015). “Consensus”+1, +2, +3 nucleosome positions downstream of the TSS were inferred from aggregate MNase-seq profiles across the genome (FIG. 1A for Oxytricha and FIG. 9A for Tetrahymena). Each gene was classified as having a +1, +2, +3 and/or +4 nucleosome if there is a called nucleosome dyad within 75 bp of the consensus nucleosome position.

[0161] RNA-seq and TSS-seq read coverage were calculated without normalization by DNA copy number since there is no correlation between Oxytricha DNA and transcript levels (Swart et al., 2013).

[0162] Oxytricha TSSs were called from TSS-seq data using CAGEr (Haberle et al., 2015); with clusterCTSS parameters (threshold=1.6, thresholdlsTpm=TRUE, nrPassThreshold=1, method=“paraclu,” removeSingletons=TRUE, keepSingletonsAbove=5). Only TSSs with tags per million counts>0.1 were used for downstream analysis. Tetrahymena TSSs were obtained from (Beh et al., 2015).

SMRT-Seq Data Processing

[0163] We processed SMRT-seq data with SMRTPipe v1.87.139483 in the SMRT Analysis 2.3.0 environment using, in order, the P Fetch, P Filter (with minLength=50, minSubreadLength=50, readScore=0.75, and artifact=−1000), P FilterReports, P Mapping (with gff2Bed=True, pulsemetrics=DeletionQV, IPD, InsertionQV, PulseWidth, QualityValue, MergeQV, SubstitutionQV, DeletionTag, and load PulseOpts=byread), P_MappingReports, P_GenomicConsensus (with algorithm=quiver, outputConsensus=True, and enableMapQVFilter=True), P_ConsensusReports, and P Mod ificationDetection (with identifyModifcations=True, enableMapQVFilter=False, and mapQvThreshold=10) modules. All other parameters were set to the default. The Oxytricha August 2013 reference genome build was used for mapping Oxytricha SMRT-seq reads, with Contig10040.0.1, Contig1527.0.1, Contig4330.0.1, and Contig54.0.1 removed, as they are perfect duplicates of other Contigs in the assembly. Tetrahymena SMRT-seq reads were mapped to the June 2014 reference genome build. Only chromosomes with high SMRT-seq coverage (>=80× for Oxytricha; >=100× for Tetrahymena) were used for all 6 mA-related analyses.

Chromosome Synthesis

[0164] Synthetic Contig1781.0 chromosomes were constructed from “building blocks” of native chromosome sequence (FIGS. 5B and 5C). The dark blue building block in FIG. 5B was prepared by annealing synthetic oligonucleotides, while all other building blocks were generated by PCR-amplification from genomic DNA using Phusion DNA polymerase (New England Biolabs). All oligonucleotides used for annealing and PCR amplification are listed in Table 2. The PCR-amplified building blocks contain terminal restriction sites for BsaI (New England Biolabs), a type IIS restriction enzyme that cuts distal from these sites. BsaI cleaves within the native DNA sequence, generating custom 4nt 5′ overhangs and releasing the non-native BsaI restriction site as small fragments that are subsequently purified away. The BsaI-generated overhangs are complementary only between adjacent building blocks, conferring specificity in ligation and minimizing undesired by-products. After BsaI digestion, PCR building blocks were purified by phenol:chloroform extraction and ethanol precipitation. Building blocks were then sequentially ligated to each other using T4 DNA ligase (New England Biolabs) and purified by phenol:chloroform extraction and ethanol precipitation. Size selection after each ligation step was performed using polyethylene glycol (PEG) precipitation or Ampure XP beads (Beckman Coulter) to enrich for the large ligated product over its smaller constituents. The size of individual building blocks and their corresponding order of ligation were designed to maximize differences in size between ligated products and individual building blocks. This increases the efficiency in size selection of products over reactants. Chromosomes 1 and 6 in FIG. 5B was generated by full length PCR from genomic DNA. To prepare chromosomes 2-4 in FIG. 5B, the red, dark blue, and purple blocks were first ligated in a 3-piece reaction and purified from the individual components. This product was subsequently ligated with the turquoise building block to obtain the full length chromosome. To prepare chromosomes 5 in FIG. 5B, the red, orange, and emerald building blocks were ligated in a 3-piece reaction and subsequently purified. All chromosomes were subjected to Sanger sequencing to verify ligation junctions. 6 mA was installed in synthetic chromosomes using annealed oligonucleotides, or by incubation of DNA building blocks with EcoGII methyltransferase (New England Biolabs).

Verification of Synthetic Chromosome Sequences

[0165] All chromosomes were dA-tailed using Klenow Fragment (3′->5′ exo-) (New England Biolabs), cloned using a TOPO TA cloning kit (Thermo Fisher) or StrataClone PCR Cloning Kit (Agilent Technologies), transformed into One Shot TOP10 chemically competent E. coli, and sequenced using flanking T7, T3, M13F, or M13R primers.

Preparation of Oxytricha Histones

[0166] Vegetative Oxytricha trifallax strain JRB310 was cultured as described in the subheading: “Experimental model and subject details” of this study. Cells were starved for 14 hr and subsequently harvested for macronuclear isolation as described in the subheading: “in vivo MNase-seq” of this study. However, formaldehyde fixation was omitted. Purified nuclei were pelleted by centrifugation at 4000×g, resuspended in 0.421 mL 0.4N H.sub.2SO.sub.4 per 10.sup.6 input cells, and nutated for 3 hr at 4° C. to extract histones. Subsequently, the acid-extracted mixture was centrifuged at 21,000× a for 15 min to remove debris. Proteins were precipitated from the cleared supernatant using trichloroacetic acid (TCA), washed with cold acetone, then dried and resuspended in 2.5% v/v acetic acid. Individual core histone fractions were purified from crude acid-extracts using semi-preparative RP-HPLC (Vydac C18, 12 micron, 10 mM×250 mm) with 40%-65% HPLC solvent B over 50 min (FIG. 13A). The identity of each purified histone fraction was verified by western analysis (FIG. 13C) using antibodies: anti-H2A (Active Motif #39111), anti-H2B (Abcam #ab1790), anti-H3 (Abcam #ab1791), anti-H4 (Active Motif #39269).

Preparation of Recombinant Xenopus Histones

[0167] All RP-HPLC analyses were performed using 0.1% TFA in water (HPLC solvent A), and 90% acetonitrile, 0.1% TFA in water (HPLC solvent B) as the mobile phases. Wild-type Xenopus H4, H3 C110A, H2B and H2A proteins were expressed in BL21(DE3) pLysS E. coli and purified from inclusion bodies through ion exchange chromatography (Debelouchina et al., 2017). Purified histones were characterized by ESI-MS using a MicrOTOF-Q II ESI-Qq-TOF mass spectrometer (Bruker Daltonics). H4: calculated 11,236 Da, observed 11,236.1 Da; H3 C110A: calculated 15,239 Da, observed 15,238.7 Da; H2A: calculated 13,950 Da, observed 13,949.8 Da; H2B: calculated 13,817 Da, observed 13,816.8 Da.

Preparation of Histone Octamers

[0168] Oxytricha and Xenopus histone octamers were respectively refolded from core histones using established protocols (Beh et al., 2015; Debelouchina et al., 2017). Briefly, lyophilized histone proteins (Xenopus modified or wild-type; Oxytricha acid-extracted) were combined in equimolar amounts in 6 M guanidine hydrochloride, 20 mM Tris pH 7.5 and the final concentration was adjusted to 1 mg/mL. The solution was dialyzed against 2M NaCl, 10 mM Tris, 1 mM EDTA, and the octamers were purified from tetramer and dimer species using size-exclusion chromatography on a Superdex 200 10/300 column (GE Healthcare Life Sciences). The purity of each fraction was analyzed by SDS-PAGE. Pure fractions were combined, concentrated and stored in 50% v/v glycerol at −20° C.

Preparation of Mini-Genome DNA

[0169] 98 full-length chromosomes were individually amplified from Oxytricha trifallax strain JRB310 genomic DNA using Phusion DNA polymerase (New England Biolabs). Primer pairs are listed in Table 2. Amplified chromosomes were separately purified using a MinElute PCR purification kit (QIAGEN), and then mixed in equimolar ratios to obtain “mini-genome” DNA. The sample was concentrated by ethanol precipitation and adjusted to a final concentration of ˜1.6 mg/mL.

Preparation of Native Genomic DNA for Chromatin Assembly Starry

[0170] Macronuclei were isolated from vegetative Oxytricha trifallax strain JRB310 as described in the subheading “in vivo MNase-seq” of this study. However, cells were not fixed prior to nuclear isolation. Genomic DNA was purified using the Nucleospin Tissue kit (Macherey-Nagel). Approximately 200 μg of genomic DNA was loaded on a 15%-40% linear sucrose gradient and centrifuged in a SW 40 Ti rotor (Beckman Coulter) at 160,070×g for 22.5 hr at 20° C. Sucrose solutions were in 1M NaCl, 20 mM Tris pH 7.5, 5 mM EDTA. Individual fractions from the sucrose gradient were analyzed on 0.9% agarose-TAE gels. Fractions containing high molecular weight DNA that migrated at the mobility limit were discarded as such DNA species were found to interfere with downstream chromatin assembly. All other fractions were pooled, ethanol precipitated, and adjusted to 0.5 mg/mL DNA.

Chromatin Assembly and Preparation of Mononucleosomal DNA

[0171] Chromatin assemblies were prepared by salt gradient dialysis as previously described (Beh et al., 2015; Luger et al., 1999), or using mouse NAP1 histone chaperone and Drosophila ACF chromatin remodeler as previously described (An and Roeder, 2004; Fyodorov and Kadonaga, 2003). Details of each chromatin assembly procedure are listed below. To reduce sample requirements while maintaining adequate DNA concentrations for chromatin assembly, synthetic chromosomes were first mixed with a hundred-fold excess of “buffer” DNA (PCR-amplified Oxytricha Contig17535.0). We verified that nucleosome occupancy in the methylated region (qPCR primer pairs 6 and 7) of the synthetic chromosome is unaffected by the presence of buffer DNA (FIG. 14E). Native and mini-genome DNA were not mixed with buffer DNA prior to chromatin assembly.

[0172] For chromatin assembly through salt dialysis: histone octamers and (synthetic chromosome+buffer) DNA were mixed in a 0.8:1 mass ratio, while histone octamers and (native or mini-genome) DNA were mixed in a 1.3:1 mass ratio, each in a 50 μL total volume. Samples were first dialyzed into start buffer (10 mM Tris pH 7.5, 1.4M KCl, 0.1 mM EDTA pH 7.5, 1 mM DTT) for 1 hr at 4° C. Then, 350 mL end buffer (10 mM Tris pH 7.5, 10 mM KCl, 0.1 mM EDTA, 1 mM DTT) was added at a rate of 1mUmin with stirring. The assembled chromatin was dialyzed overnight at 4° C. into 200 mL end buffer, followed by a final round of dialysis in fresh 200 mL end buffer for 1 hr at 4° C. The assembled chromatin was then adjusted to 50 mM Tris pH 7.9, 5 mM CaCl.sub.2) and digested with MNase (New England Biolabs) to mainly mononucleosomal DNA as previously described (Beh et al., 2015).

[0173] For chromatin assembly using mouse NAP1 and Drosophila ACF: NAP1 was recombinantly expressed and purified as described in (An and Roeder, 2004). ACF was purchased from Active Motif. 0.49 μM NAP1 and 58 nM histone octamer were first mixed in a 302p1 reaction volume containing 62 mM KCl, 1.2% w/v polyvinyl alcohol (Sigma Aldrich), 1.2% w/v polyethylene glycol 8000 (Sigma Aldrich), 25 mM HEPES-KOH pH 7.5, 0.1 mM EDTA-KOH, 10% v/v glycerol, and 0.01% v/v NP-40. The NAP1-histone mix was incubated on ice for 30 min. Meanwhile, “AM” mix was prepared, consisting of 20 mM ATP (Sigma Aldrich), 200 mM creatine phosphate (Sigma Aldrich). 33.3 mM MgCl.sub.2, 33.3 μg/μl creatine kinase (Sigma Aldrich) in a 56u1 reaction volume. After the 30 min incubation. 5.29 μl of 1.7 μM ACF complex (Active Motif) and the “AM” mix were sequentially added to the NAP1-histone mix. Then, 10.63 μl of native or mini-genome DNA (2.66 μg) was added, resulting in a 374 μl reaction volume. The final mixture was incubated at 27° C. for 2.5 hr to allow for chromatin assembly. Subsequently, CaCl.sub.2 was added to a final concentration of 5 mM, and the chromatin was digested with MNase (New England Biolabs) to mainly mononucleosomal DNA as previously described (Beh et al., 2015).

[0174] Mononucleosome-sized DNA from MNase-digested chromatin was gel-purified and used for tiling qPCR on a Viia 7 Real-Time PCR System with Power SYBR Green PCR master mix (Thermo Fisher), or in vitro MNase-seq on an Illumina HiSeq 2500, according to the manufacturer's instructions. qPCR primer sequences are listed in Table 2.

Tiling qPCR Analysis of Nucleosome Occupancy

[0175] qPCR data were analyzed using the ΔΔCt method (Livak and Schmittgen, 2001). At each locus along the synthetic chromosome, ΔCt=(Ct at locus of interest)−(Ct at qPCR primer pair 22, far from the methylated region). See FIG. 6B for location of qPCR primer pair 22. Separate ΔCt values were calculated from mononucleosomal DNA and the corresponding naked, undigested synthetic chromosome. The ΔΔCt value was calculated from this pair of ΔCt values. This controls for potential variation in PCR amplification efficiency, especially over methylated regions. The fold change in mononucleosomal DNA relative to naked chromosomal DNA at a particular locus is calculated as 2.sup.−ΔΔCt, and denotes ‘nucleosome occupancy’ for all presented qPCR data.

ACF Spacing Assay

[0176] ATP-dependent nucleosome spacing was performed in accordance with a previous study (Lieleg et al., 2015). Chromatin was assembled by salt gradient dialysis as described above, and then adjusted to 20 mM HEPES-KOH pH 7.5, 80 mM KCl, 0.5 mM EGTA, 12% v/v glycerol, 10 mM (NH.sub.4).sub.2SO.sub.4, 2.5 mM DTT. Samples were then incubated for 2.5 hr at 27° C. with 3 mM ATP, 30 mM creatine phosphate, 4 mM MgCl.sub.2, 5 ng/0 creatine kinase, and 11 ng/μL ACF complex (Active Motif). Remodeled chromatin was then adjusted to 5 mM CaCl.sub.2) and subjected to MNase digestion, mononucleosomal DNA purification, and qPCR analysis as described above.

Phylogenetic Analysis

[0177] The MTA1 amino acid sequence (UniProt ID: J9IF92 9SPIT) was queried against the NCBI nr database using PSI-BLAST (Altschul et al., 1997; Schaffer et al., 2001) (maximum e-value=1e.sup.−4; enable short queries and filtering of low complexity regions). Retrieved hits were collapsed using CD-HIT (Huang et al., 2010) with minimum sequence identity=0.97 to remove redundant sequences. The resulting sequences were added to existing MT-A70 alignments from (Greer et al., 2015) using MAFFT (-add) (Katoh et al., 2017; Kuraku et al., 2013). Gaps and duplicate sequences were removed from the merged alignment. Only sequences corresponding to the taxa in FIG. 2B were retained. The alignment was then used for phylogenetic tree construction using MrBayes in the CIPRES Science Gateway (Miller et al., 2010) with 5×10.sup.6 generations. Protein sequences used for MrBayes analysis are given in Table 1.

[0178] The above procedure was also used for constructing phylogenetic trees from p1 (UniProt ID: Q22VV9 TETTS) and p2 (UniProt ID: I7M8B9 TETTS). However, protein sequences were aligned using MAFFT without adding to an existing alignment.

Preparation of Nuclear Extracts with DNA Methyltransferase Activity

[0179] Vegetative Tetrahymena cells were grown in SSP medium to log-phase (˜3.5×10.sup.6 cells/mL) and collected by centrifugation at 2,300×g for 5 min in an SLA-3000 rotor. The supernatant was discarded, and cells were resuspended in medium B (10 mM Tris pH 6.75, 2 mM MgCl.sub.2, 0.1M sucrose, 0.05% w/v spermidine trihydrochloride, 4% w/v gum Arabic, 0.63% w/v 1-octanol, and 1 mM PMSF). Gum arabic (Sigma Aldrich) is prepared as a 20% w/v stock and centrifuged at 7,000×g for 30 min to remove undissolved clumps. For each volume of cell culture, one-third volume of medium B was added to the Tetrahymena cell pellet. Cells were resuspended and homogenized in a chilled Waring Blender (Waring PBB212) at high speed for 40 s. The resulting lysate was subsequently centrifuged at 2,750×g for 5 min in an SLA-3000 rotor to pellet macronuclei. The nuclear pellet was washed twice with medium B and then five times in MM medium (10 mM Tris-HCl pH 7.8, 0.25M sucrose, 15 mM MgCl.sub.2, 0.1% w/v spermidine trihydrochloride, 1 mM DTT, 1 mM PMSF). Macronuclei were pelleted between wash steps by centrifuging at 2,500×g for 5 min in an SLA-3000 rotor. Finally, the total number of washed macronuclei was counted with a hemocytometer using a Zeiss ID03 microscope. Nuclear proteins were extracted by vigorously resuspending the pellet in M M salt buffer (10 mM Tris-HCl pH 7.8, 0.25M sucrose, 15 mM MgCl2, 350 mM NaCl, 0.1% w/v spermidine trihydrochloride, 1 mM DTT, 1 mM PMSF). 1 mL M M salt buffer was added per 2.33×108 macronuclei. The viscous mixture was nutated for 45 min at 4° C., and then cleared at 175,000×g for 30 min at 4° C. in a SW 41 Ti rotor. Following this, the supernatant was dialyzed in a Slide-A-Lyzer 3.5K MWCO cassette (Thermo Fisher) overnight at 4° C. against two changes of MM minus medium (10 mM Tris-HCl pH 7.8, 15 mM MgCl.sub.2, 1 mM DTT, 0.5 mM PMSF). The dialysate was then centrifuged at 7,197×g for 1 hr at 4″C to remove precipitates, and dialyzed overnight in a Slide-A-Lyzer 3.5K MWCO cassette (Thermo Fisher) at 4° C. against two changes of MN3 buffer (30 mM Tris-HCl pH 7.8, 1 mM EDTA, 15 mM NaCl, 20% v/v glycerol, 1 mM DTT, 0.5 mM PMSF). The final dialysate was cleared by centrifugation at 7,197 g for 1.5 hr at 4° C., flash frozen, and stored at −80° C. This nuclear extract was used for all subsequent biochemical fractionation and 6 mA methylation assays.

Partial Purification of MTA1c from Nuclear Extracts

[0180] Tetrahymena nuclear extracts were passed through a HiTrap O HP column (GE Healthcare) and eluted using a linear aradient of 15 mM to 650 mM NaCl in 30 mM Tris-HCl pH 7.8, 1 mM EDTA, 20% v/v glycerol, 1 mM DTT, 0.5 mM PMSF, over 30 column volumes. Each fraction was assayed for DNA methyltransferase activity using radiolabeled SAM as described in the next section. The DNA methyltransferase activity eluted in two peaks, at ˜60 mM and ˜365 mM NaCl, termed the “low salt sample” and “high salt sample.” Fractions corresponding to each peak were pooled and passed through a HiTrap Heparin HP column (GE Healthcare). Bound proteins were eluted using a linear gradient of 60 mM to 1M NaCl (for the low salt sample) or 350 mM to 1M NaCl (for the high salt sample) over 30 column volumes. Fractions with DNA methyltransferase activity were respectively pooled and dialyzed into 10 mM sodium phosphate pH 6.8, 100 mM NaCl, 10% v/v glycerol, 0.3 mM CaCl.sub.2), 0.5 mM DTT (for the low salt sample); or 30 mM Tris-HCl pH 7.8, 1 mM EDTA, 200 mM NaCl, 10% v/v glycerol, 1 mM DTT, 0.2 mM PMSF (for the high salt sample). The dialyzed low salt sample was passed through a Nuvia cPrime column (Bio-Rad) and eluted using a linear gradient of 100 mM to 1M NaCl in 50 mM sodium phosphate pH 6.8, 10% v/v glycerol, 0.5 mM DTT. Separately, the dialyzed high salt sample was fractionated using a Superdex 200 10/300 GL column (GE Healthcare) in 30 mM Tris-HCl pH 7.8, 1 mM EDTA, 200 mM NaCl, 10% v/v glycerol, 1 mM DTT. Fractions from the Nuvia cPrime and Superdex 200 columns were dialyzed into 30 mM Tris-HCl pH 7.8, 1 mM EDTA, 15 mM NaCl, 20% v/v glycerol, 1 mM DTT, 0.5 mM PMSF and assayed for DNA methyltransferase activity. Those with qualitatively low, medium, and high activity were subjected to mass spectrometry to identify candidate methyltransferase proteins (FIG. 2D; Table 6). This experiment identified four proteins that co-purify with DNA methyltransferase activity—MTA1, MTA9, p1, and p2—and are collectively termed as “MTA1c” in the present disclosure. All four proteins are necessary for 6 mA methylation in vitro.

Recombinant Expression of MTA1, MTA9, p1, and p2 Proteins

[0181] Full length MTA1, MTA9, p1, and p2 open reading frames were codon-optimized for bacterial expression and cloned into a pET-His6-SUMO vector using ligation independent cloning. Protein sequences are listed in Table 3. The vector was a gift from Scott Gradia (Addgene plasmid #29659; http://addgene.org/29659; RRID: Addgene 29659). Mutations in the MTA1 open reading frame was introduced using the OS® Site-Directed Mutagenesis Kit (New England Biolabs). For recombinant expression, pET-His6-SUMO-MTA1 (wild-type and mutant) was transformed into SHuffle T7 competent E. co/i (New England Biolabs); pET-His6-SUMO-MTA9 was transformed into Lemo (DE3) competent E. coli (New England Biolabs); pET-His6-SUMO-p1 and pET-His6-SUMO-p2 were transformed into BL21(DE3) competent E. coli (New England Biolabs). IPTG induction was performed at 16′C overnight. Induced cells were resuspended in 25 ml of lysis buffer B (50 mM Tris pH 7.8, 300 mM NaCl, 5% v/v glycerol, 10 mM imidazole, 5 mM BME, 1 mM PMSF, 0.5× ProBlock Gold Bacterial protease inhibitor cocktail [GoldBio]). The cells were sonicated at 35% amplitude for a total of 4 minutes, with a 10 s off, 10 s cycle using a Model 505 Sonic Dismembrator (Fisherbrand). Lysates were cleared by centrifugation at 30,000 g for 30 min at 4° C., mixed with pre-washed Ni-NTA agarose (Invitrogen), and nutated for 45 min at 4° C. The resin was subsequently washed with lysis buffer and eluted in 50 mM Tris pH 7.8, 300 mM NaCl, 5% v/v glycerol, 400 mM glycerol, 5 mM BME, lx ProBlock Gold bacterial protease inhibitor cocktail [GoldBio]). Eluates were dialyzed into lysis buffer B and then digested with TEV protease (gift from S.H. Sternberg) at 4° C. overnight. The resulting mixture was passed through a fresh batch of Ni-NTA agarose (Invitrogen) to remove cleaved affinity tags. The flow-through containing each recombinant protein was flash frozen and used for all downstream methyltransferase assays.

Methyltransferase Assays

Generation of DNA and RNA Substrates

[0182] A 954 bp dsDNA PCR product was used in all assays involving Tetrahymena nuclear extract. This substrate was amplified by PCR from Tetrahymena thermophila strain SB210 macronuclear SB210 genomic DNA using PCR primers metGATC F2 and metGATC_R2 (Table 2). The resulting product was purified using Ampure XP beads (Beckman Coulter). This 954 bp region of the genome contains a high level of 6 mA in vivo. Thus, the underlying DNA sequence may be intrinsically amenable to methylation by Tetrahymena MTA1. Note that the amplified 954 bp product is devoid of DNA methylation as unmodified dNTPs were used for PCR. Separately, a 350 bp dsDNA PCR product was used in all assays involving recombinant MTA1, MTA9, p1 and p2. This sequence lacks 5′-NATC-3′ motifs, and was used to reduce background DNA methylation from contaminating Dam methyltransferase in recombinant protein preparations. The 350 bp dsDNA PCR product was amplified from Tetrahymena thermophila strain SB210 macronuclear SB210 genomic DNA using the PCR primers noGATC2 F and noGATC2_R (Table 2), and purified using Ampure XP beads (Beckman Coulter).

[0183] For short DNA substrates (<50 bp), oligonucleotides were purchased from Integrated DNA Technologies and either directly used as ssDNA, or annealed with its complementary sequence to obtain dsDNA. To prepare hemimethylated 27 bp dsDNA in FIG. 2G, either strand was methylated using EcoGII methyltransferase (New England BioLabs) before annealing with the complementary sequence.

[0184] To generate ˜350nt ssRNA and −350 bp dsRNA, the aforementioned 350 bp dsDNA was first PCR-amplified using primers containing T7 overhangs (primer pairs T7noGATC2_F2/noGATC2_R and T7noGATC2_F2/T7noGATC2_R2 respectively; see Table 2 for primer sequences). Each PCR product was used as a template for in vitro transcription using the HiScribe T7 High Yield RNA Synthesis Kit (New England Biolabs). The synthesized RNA was rigorously treated with DNase (ThermoFisher) purified using acid phenol:chloroform extraction, followed by two rounds of chloroform extraction. Each sample was subsequently ethanol precipitated and resuspended in water for use in methyltransferase assays.

Radioactive Methyltransferase Assay

[0185] For experiments involving nuclear extract, 2.18 μg of 954 bp dsDNA substrate was mixed with 4-8 μl nuclear extract and 0.64 μM 3H-labeled S-adenosyl-L-methionine ([.sup.3H]SAM) in 33 mM Tris-HCl pH 7.5. 6 mM EDTA. 4.3 mM BME. in a 15p1 reaction volume. For experiments involving recombinant MTA1c protein components (ie. MTA1, MTA9, p1, and/or p2), ˜3 μM oligonucleotide ssDNA/annealed dsDNA is used. Alternatively, 1.3 μg of 350 bp dsDNA substrate (or an equimolar amount ˜350nt ssRNA, or ˜350 bp dsDNA) was used in place of DNA oligonucleotide substrates. ssRNA was heated at 90° C. for 2 min and snap cooled to minimize secondary structures before mixing with other components of the methyltransferase assay. All samples were incubated overnight at 37° C., and subsequently spotted onto 1 cm×1 cm squares of Hybond-XL membrane (GE Healthcare). Membranes were then washed thrice with 0.2M ammonium bicarbonate, once with distilled water, twice with 100% ethanol, and finally air-dried for 1 hr. Each membrane was immersed in 5 mL Ultima Gold (PerkinElmer) and used for scintillation counting on a TriCarb 2910 TR (Perkin Elmer).

Non-Radioactive Methyltransferase Assay

[0186] For assays involving nuclear extract: 5.5 pg of 954 bp DNA substrate was mixed with 20 nuclear extract and 0.2 mM S-adenosyl-L methionine (NEB) in 33 mM Tris-HCl pH 7.5, 6 mM EDTA, 4.3 mM BME in a 15p1 reaction volume. For assays involving recombinant MTA1c protein components (ie. MTA1, MTA9, p1, and/or p2), 2.6 μg of 350 bp DNA substrate was mixed with 540 nM MTA1, 90 nM MTA9, 1.5 μM p1, 1.0 μM p2 proteins. The band of expected size in each recombinant protein preparation was compared against a series of BSA standards to calculate protein concentration. All methylation reactions were incubated at 37° C. overnight, then purified using a MinElute purification kit (QIAGEN), denatured at 95° C. for 10 min, and snap cooled in an ice water bath. Samples were spotted on a Hybond N+ membrane (GE Healthcare), air-dried for 5 min and UV-cross-linked with 120,000 μJ/cm.sup.2 exposure using an Ultra-Lum UVC-515 Ultraviolet Multilinker. The cross-linked membrane was blocked in 5% milk in TBST (containing 0.1% v/v Tween) and incubated with 1:1,000 anti-N6-methyladenosine antibody (Synaptic Systems) at 4° C. overnight. The membrane was then washed three times with TBST, incubated with 1:3,000 Goat anti-rabbit HRP antibody (Bio-Rad) at room temperature for 1 hr, washed another three times with 1×TBST, and developed using Amersham ECL Western Blotting Detection Kit (GE Healthcare). This dot blot assay was used to measure 6 mA levels in FIGS. 2F, 3B, 5C, and 10C.

Quantitative Mass Spectrometry Analysis of dA and 6 mA

[0187] 10.5 μg Oxytricha or Tetrahymena macronuclear genomic DNA was first digested to nucleosides by mixing with 14p1 DNA degradase plus enzyme (Zymo Research) in a 262.5 μl reaction volume. Samples were incubated at 37° C. overnight, then 70° C. for 20 min to deactivate the enzyme.

[0188] The internal nucleoside standards .sup.15N.sub.5-dA and D.sub.3-6 mA were used to quantify endogenous dA and 6 mA levels in ciliate DNA. .sup.15N.sub.5-dA was purchased from Cambridge Isotope Laboratories, while D.sub.3-6 mA was synthesized as described in the following section. Nucleoside samples were spiked with 1 ng/μl .sup.15N.sub.5-dA and 200 pg/μl D.sub.3-6 mA in an autosampler vial. Samples were loaded onto a 1 mm×100 mm C18 column (Ace C18-AR, Mac-Mod) using a Shimadzu HPLC system and PAL auto-sampler (20 μl/injection) at a flow rate of 70 μl/min. The column was connected inline to an electrospray source couple to an LTQ-Orbitrap XL mass spectrometer (Thermo Fisher). Caffeine (2 pmol/μl in 50% Acetonitrile with 0.1% FA) was injected as a lock mass through a tee at the column outlet using a syringe pump at 0.5p1/min (Harvard PHD 2000). Chromatographic separation was achieved with a linear gradient from 10% to 99% B (A: 0.1% Formic Acid, B: 0.1% Formic Acid in Acetonitrile) in 5 min, followed by 5 min wash at 100% B and equilibration for 10 min with 1% B (total 20 min program). Electrospray ionization was achieved using a spray voltage of 4.50 kV aided by sheath gas (Nitrogen) flow rate of 18 (arbitrary units) and auxiliary gas (Nitrogen) flow rate of 2 (arbitrary units). Full scan MS data were acquired in the Orbitrap at a resolution of 60,000 in profile mode from the m/z range of 190-290. A parent mass list was utilized to acquire MS/MS spectra at a resolution of 7500 in the Orbitrap. LC-MS data were manually interpreted in Xcalibur's Qual browser (Thermo, Version 2.1) to visualize nucleoside mass spectra and to generate extracted ion chromatograms by using the theoretical [M+H] within a range of ±2 ppm. Peak areas were extracted in Skyline (Ver. 3.5.0.9319).

Synthesis of D.SUB.3.-6 mA Nucleoside

[0189] 2′-Deoxyadenosine and CD3I were purchased from Sigma Aldrich. Flash chromatography was performed on a Biotage Isolera using silica columns (Biotage SNAP Ultra, HP-Sphere 25 pm). Semi-preparative RP-HPLC was performed on a Hewlett-Packard 1200 series instrument equipped with a Waters XBridge BEH C18 column (5 μm, 10×250 mm) at a flow rate of 4 mL/min, eluting using A (0.1% formic acid in H.sub.2O) and B (0.1% formic acid in 9:1 MeCN/H.sub.2O). .sup.1H NMR spectra were recorded on a Bruker UltraShield Plus 500 MHz instrument. Data for .sup.1H NMR are reported as follows: chemical shift (8 ppm), multiplicity (s=singlet, br=broad signal, d=doublet, dd=doublet of doublets) and coupling constant (Hz) where possible. .sup.13C NMR spectra were recorded on a Bruker UltraShield Plus 500 MHz.

[0190] D.sub.3-6 mA (2′Deoxy-6-[D3]-methyladenosine) were synthesized and purified according to (Schiffers et al., 2017). After an initial purification by flash column chromatography, the methylated compounds were further purified by semipreparative RP-HPLC (linear gradient of 0% to 20% B over 30 min) affording the desired compounds in 14% and 10% yields respectively after lyophilization.

2Deoxy-6-[D3]methyladenosine

[0191] .sup.1H NMR (500 MHz, D.sub.2O) δ 7.98 (s, 1H), 7.77 (s, 1H), 6.17 (m, 1H), 4.54 (m, 1H), 4.10 (m, 1H), 3.79 (dd, J=12.7, 3.2 Hz, 1H), 3.71 (dd, J=12.7, 4.3 Hz, 1H), 2.60 (m, 1H), 2.44 (ddd, J=14.0, 6.3, 3.3 Hz, 1H).

[0192] .sup.13C NMR (126 MHz, D.sub.2O) δ 154.0, 151.5, 146.1, 138.9, 118.4, 87.3, 84.3, 71.1, 61.6, 39.2, 26.4 ppm. (Peak at 26.4 ppm appears as a broad signal. C-D coupling is not resolved).

[0193] HR-MS (ESI+): m/z calculated for [C.sub.11H.sub.13D.sub.3N.sub.5O.sub.3].sup.+ ([M+Hr): 269.1436. found 269.1421.

Mass Spectrometry Analysis of Proteins in Tetrahymena Nuclear Extracts

[0194] Samples where topped up to 200p1 with 50 mM ammonium bicarbonate pH 8. TCEP was added to 5 mM final concentration and left to incubate at 60° C. for 10 min. 15 mM chloroacetamide was then added and left to incubate in the dark at room temperature for 30 min. 1 μg of Trypsin Gold (Promega) was added to each sample and incubated end-over-end at 37° C. for 16 hr. An additional 0.25 μg of Trypsin Gold was added and incubated end-over-end at 37° C. for 3 hr. Samples were acidified by adding TFA to 0.2% final concentration, and desalted using SDB stage-tips (Rappsilber et al., 2007). Samples were dried completely in a speedvac and resuspended in 20p1 of 0.1% formic acid pH 3.5 μl was injected per run using an Easy-nLC 1200 UPLC system. Samples were loaded directly onto a 45 cm long 75 pm inner diameter nano capillary column packed with 1.9 μm C18-AQ (Dr. Maisch, Germany) mated to metal emitter in-line with an Orbitrap Fusion Lumos (Thermo Scientific, USA). The mass spectrometer was operated in data dependent mode with the 120,000 resolution MS1 scan (AGC 4e5, Max IT 50 ms, 400-1500 m/z) in the Orbitrap followed by up to 20 MS/MS scans with CID fragmentation in the ion trap. Dynamic exclusion list was invoked to exclude previously sequenced peptides for 60 s if sequenced within the last 30 s, and maximum cycle time of 3 s was used. Peptides were isolated for fragmentation using the quadrupole (1.6 Da window). Ns was utilized. Ion-trap was operated in Rapid mode with AGC 2e3, maximum IT of 300 msec and minimum of 5000 ions.

[0195] Raw files were searched using Byonic (Bern et al., 2012) and Sequest HT algorithms (Eng et al., 1994) within the Proteome Discoverer 2.1 suite (Thermo Scientific, USA). 1 Oppm MS1 and 0.4 Da MS2 mass tolerances were specified. Caramidomethylation of cysteine was used as fixed modification, while oxidation of methionine, pyro-Glu from Gln and deamidation of asparagine were specified as dynamic modifications. Trypsin digestion with maximum of 2 missed cleavages were allowed. Files were searched against the Tetrahymena themophila macronuclear reference proteome (June 2014 build), supplemented with common contaminants (27,099 total entries).

[0196] Scaffold (version Scaffold 4.8.7, Proteome Software Inc., Portland, Oreg.) was used to validate MS/MS based peptide and protein identifications. Peptide identifications were accepted if they could be established at greater than 93.0% probability. Peptide Probabilities from Sequest and Byonic were assigned by the Scaffold Local FDR algorithm. Protein identifications were accepted if they could be established at greater than 99.0% probability to achieve an FDR less than 1.0% and contained at least 3 identified peptides. Protein probabilities were assigned by the Protein Prophet algorithm (Nesvizhskii et al., 2003). Proteins that contained similar peptides and could not be differentiated based on MS/MS analysis alone were grouped to satisfy the principles of parsimony.

Generation of Mta1 Mutant Lines

[0197] A frameshift mutation in the MTA1 gene was created by inserting a small non-coding DNA segment immediately downstream of the MTA1 start codon (FIGS. 3A and 12H). This non-coding DNA segment belongs to a class of genetic elements that are normally eliminated during the sexual cycle (Chen et al., 2014). When ssRNA homologous to such DNA segments is injected into Oxytricha cells undergoing sexual development, the DNA is erroneously retained (Khurana et al., 2018). This results in disruption of the MTA1 open reading frame. The ectopic DNA segment is propagated through subsequent cell divisions after completion of the sexual cycle. RNaseq analysis confirmed the presence of the ectopic insertion in mta1 mutant transcripts but not wild-type controls (FIG. 12H).

[0198] ssRNA was generated by in vitro transcription using a Hi-Scribe T7 High Yield RNA Synthesis Kit (New England Biolabs). The DNA template for in vitro transcription consists of the ectopic DNA segment flanked by 100-200 bp cognate MTA1 sequence. Following DNase treatment, ssRNA was acid-phenol:chloroform extracted and ethanol precipitated. After precipitation, ssRNA was resuspended in nuclease-free water (Ambion) to a final concentration of 1 to 3 mg/mL for injection.

ssRNA Microinjections

[0199] Oxytricha cells were mated by mixing 3 mL of each mating type, JRB310 and JRB510, along with 6 mL of fresh Pringsheim media. At 10 to 12 hr post mixing, pairs were isolated and placed in Volvic water with 0.2% bovine serum albumin (Jackson ImmunoResearch Laboratories) (Fang et al., 2012). ssRNA constructs were injected into the macronuclei of paired cells under a light microscope as previously described with DNA constructs (Nowacki et al., 2008). After injection, cells were pooled in Volvic water. At 60 to 72 hr post mixing, the pooled cells were singled out to grow clonal injected cell lines. As clonal population size grew, lines were transferred to 10 cm Petri dishes and grown in Pringsheim media. Only water from the “Volvic” brand has been empirically tested in our laboratory to support Oxytricha growth. Similar products from other vendors have not been tested.

Survival Analysis of Oxytricha Mta1 Mutants

[0200] This experiment was performed in FIG. 7D. Wild-type or mutant Oxytricha cells were mixed at 0 hr to induce mating. Since not all cells enter the sexual cycle, mated cells are separated from unmated vegetative cells at 15 hr and transferred into a separate dish. The cells are allowed to rest for 12 hr to account for cell death during transfer. The number of surviving mated cells is counted from 27 hr onward. The total cell number at each time point is normalized to 27 hr data to obtain the percentage survival. An increase in survival at 108 hr is observed in wild-type samples because the cells have completed mating and reverted to the vegetative state, where they can proliferate and increase in number.

Quantification and Statistical Analysis

[0201] All statistical tests were performed in Python (v2.7.10) or R (v3.2.5), and described in the respective Figure and Table legends.

Data and Software Availability

[0202] Oxytricha SMRT-seq data are deposited in SRA under the accession numbers SRA: SRX2335608 and SRX2335607, and GEO: GSE94421. Tetrahymena SMRT-seq and all Oxytricha Illumina data are deposited in NCBI GEO under accession number GEO: GSE94421.

TABLE-US-00002 TABLE 1 Protein sequences for phylogenetic tree construction. Protein sequences for phylogenetic analysis of MT-A70 proteins (including MTA1 and MTA9) >NP_495127.1 DNA N6-methyl methyltransferase [Caenorhabditis elegans] (SEQ ID No: 1) MDTEFAILDEEKYYDSVFKELNLKTRSELYEISSKFMPDSQFEAIKRRGISNRKRKIKETSENSNRMEQMALKIKNVG TELKIFKKKSILDNNLKSRKAAETALNVSIPSASASSEQIIEFQKSESLSNLMSNGMINNWVRCSGDKPGIIENSDGTK FYIPPKSTFHVGDVKDIEQYSRAHDLLFDLIIADPPWFSKSVKRKRTYQMDEEVLDCLDIPVILTHDALIAFWITNRIGI EEEMIERFDKWGMEVVATWKLLKITTQGDPVYDFDNQKHKVPFESLMLAKKKDSMRKFELPENFVFASVPMSVHS HKPPLLDLLRHFGIEFTEPLELFARSLLPSTHSVGYEPFLLQSEHVFTRNISL >NP_564080.1 Methyltransferase MT-A70 family protein [Arabidopsis thaliana] (SEQ ID No: 2) MAKTDKLAQFLDSGIYESDEFNWFFLDTVRITNRSYTRFKVSPSAYYSRFFNSKQLNQHSSESNPKKRKRKQKNSS FHLPSVGEQASNLRHQEARLFLSKAHESFLKEIELLSLTKGLSDDNDDDDSSLLNKCCDDEVSFIELGGVWQAPFYE ITLSFNLHCDNEGESCNEQRVFQVFNNLVVNEIGEEVEAEFSNRRYIMPRNSCFYMSDLHHIRNLVPAKSEEGYNLI VIDPPWENASAHQKSKYPTLPNQYFLSLPIKQLAHAEGALVALWVTNREKLLSFVEKELFPAWGIKYVATMYWLKV KPDGTLICDLDLVHHKPYEYLLLGYHFTELAGSEKRSDFKLLDKNQIIMSIPGDFSRKPPIGDILLKHTPGSQPARCLE >ORY94237.1 MT-A70-domain-containing protein [Syncephalastrum racemosum] (SEQ ID No: 3) MIVASSDTCDIVDCEAAFGIDGTVRLRPGDFSLGTPYFTSRLGQKRPRPDDDTLDNTPSDTIHAIVQQLPVMAPDY WHDRPMEAVVMNAHVHFPSLVSLAEASLRFDPDNDEDEDNRQILRPDMALESLQVFYRHFEHPKDSPILIRVQDAY YWIPPRTAFMMGSLENIHLPTLGKFDCIVMDPPWPNKSVRRSAHYETQEDIYDLFAIPLPQLAQPNCLVAVWVTNK PKFIRFVQKLFAAWDVEPLTTWYWLKVTTHGEPVCPIDSPHRKPYEHLILGRKRPVKININDPPALPRVLVSVPSKH HSRKPPLNDILMRYLPSDARRLELFARCLTPGWTSWGNECLKFQHVDYFYDTNEAMEEGKQK >ORX58127.1 MT-A70-domain-containing protein [Hesseltinella vesiculosa] (SEQ ID No: 4) MANAARRFAQQDELPLDVSQDLQDLPLLDLFNRKVINDSDQCSSLHVASFGQYLVPRHTKFVMSDLDNIDLLRSEN DVFDLIVMDPPWPNKSVHRSTDYETQDIYDLFHLPIKSLIKNQGLVAVWVTNKPKYRRFILDKLFKAWQMTCVGEW LWLKVTSSGEPVFPLDSPHRKPYEQLILGRYQPDDTSPTLPNPPQQHVLISVPSIRHSRKPPLGEVLADFLPKQPAC LELFARCLTPGWTSWGNECLKFQHESYFISNDTPHSPSAS >ORZ15132.1 MT-A70-like protein, partial [Absidia repens] (SEQ ID No: 5) YDLVVMDPPWPNKSVHRSSHYETQDIYDLYQIPLTSLVHKNSLVAVWITNKPKYRRFVMDKLFKSWHVDCVAEWT WLKVTNDGEPVFPLNSTHRKPYEQLIIGRYNGGSGGGNDNNDSIQEESEVKPIPYQHSIVSVPSKRHSRKPPLQDL LQPYLPAKPRCLELFARCLTPGWSSWGNECLKFQNEYYYTRIENPLHIDRSDV >XP_021679935.1 MT-A70-domain-containing protein [Lobosporangium transversale] (SEQ ID No: 6) MLHESTVSVLDRLILISHISLQTYLLAKDREGFDIIVMDPPWQNASVDRMSHYRTMDLYELFKIPIPDLLKANGSNVG GIVAVWITNKAKVKRVVVEKLFPAWGLDLVAHWFWLKVTTKGEPVLSLSNSHRRAYEGVLIGRQRQGSKLSNKTM HETSASNPVNRLLVSIPAQHSRKPSLNALIEEEFFTSKLESRADRDRNAYVDSEALVKKPLYRLELFARNLEEGVLS WGNEPLRYQYCGRGASNSQVVQDGYLIPCPIQSELVSQ >XP_689178.3 methyltransferase-like protein 4 isoform X1 [Danio rerio] (SEQ ID No: 7) MSVVCCNSWGWLLDSSSHIDKDFQRCVCYNEANGLEENTHFTCCFKRQYFNILMPHMQQSTAMSGFPLDSGKH DSAEHEKIELQTRKKRKRKHHDLNTGEIEANIYHDKVRSVVLEGSRALLEAGRQCGYFTEALTESQTISTPSESTSA HECQLAAFCDLAKQLPLSEESPVHTLSRDGQNPALDLFSSITENPFDCACEITFMRERYLLPPRCRFLLSDVTRMDP LVNSGDKFDLIVLDPPWENKSVKRSNRYSSLPSSQLKKLPVPALAAPGGLVVTWVTNRAKHRRFVREELYPHWAV EVLAEWLWVKVTRSGEFVFPLDSQHKKPYEVLVLGRCRSTSDHTDRCSAVNELPDQRLLVSVPSTLHSHKPSLAA VLKPYIRREPRCLELFARSLQSDWSCWGNEVLKFQHCSYFSRHTDQEPTSDTLQRTHSHLQSTGLLETPETAR >NP_073751.3 methyltransferase-like protein 4 isoform 1 [Homo sapiens] (SEQ ID No: 8) MSVVHQLSAGWLLDHLSFINKINYQLHQHHEPCCRKKEFTTSVHFESLQMDSVSSSGVCAAFIASDSSTKPENDDG GNYEMFTRKFVFRPELFDVTKPYITPAVHKECQQSNEKEDLMNGVKKEISISIIGKKRKRCVVFNQGELDAMEYHTKI RELILDGSLQLIQEGLKSGFLYPLFEKQDKGSKPITLPLDACSLSELCEMAKHLPSLNEMEHQTLQLVEEDTSVTEQD LFLRVVENNSSFTKVITLMGQKYLLPPKSSFLLSDISCMQPLLNYRKTFDVIVIDPPWQNKSVKRSNRYSYLSPLQIQ QIPIPKLAAPNCLLVTWVTNRQKHLRFIKEELYPSWSVEVVAEWHWVKITNSGEFVFPLDSPHKKPYEGLILGRVQE KTALPLRNADVNVLPIPDHKLIVSVPCTLHSHKPPLAEVLKDYIKPDGEYLELFARNLQPGWTSWGNEVLKFQHVDY FIAVESGS >XP_020951799.1 methyltransferase-like protein 4 isoform X1 [Sus scrofa] (SEQ ID No: 9) MSVVHQLSSGWLLDHLSFINKISYELHQHHEPCCSKNEPTSVHLDSLHKDSVFSFGASPAFIASSSKPENDDGGNR EMSMQKYVFRSELFDVTKPYITSAIHKECQQSNEKEDLANDVKKEASISIKRKKRKRCVVFNQGELDAMEYHTKIRG LILDGSSQLIQEGLKSGFLHPLSEKCDKCSKPVTLPLDTCSLSELCEMAKHVPSLNEMELQTLQLMEDDISVTEQDLF SRIVENNSSFTKMITLMGQKYLLPPKSSFLLSDISCIYPLLNCRKTYDVIVIDPPWQNKSVKRSNRYSYLSPLQIKQIPI PKLAAPNCLVVTWVTNRQKHLRFVKEELYPSWSVEIVAEWHWVKITNSGEFVFPIDSPHKKPYEVLVLGRVRERAA LLLSRNAEVKELSIPDRKLIVSVPCILHSHKPPLAEVLKDYIKPEGEYLELFARNLQPGWTSWGNEVLKFQHMDYFVA LESRS >XP_011245012.1 PREDICTED: methyltransferase-like protein 4 isoform X2 [Mus musculus] (SEQ ID No: 10) MSVVHHLPPGWLLDHLSFINKVNYQLCQHQESFCSKNNPTSSVYMDSLQLDPGSPFGAPAMCFAPDFTTVSGND DEGSCEVITEKYVFRSELFNVTKPYIVPAVHKERQQSNKNENLVTDYKQEVSVSVGKKRKRCIAFNQGELDAMEYH TKIRELILDGSSKLIQEGLRSGFLYPLVEKQDGSSGCITLPLDACNLSELCEMAKHLPSLNEMELQTLQLMGDDVSVI ELDLSSQIIENNSSFSKMITLMGQKYLLPPQSSFLLSDISCMQPLLNCGKTFDAIVIDPPWENKSVKRSNRYSSLSPQ QIKRMPIPKLAAADCLIVTWVTNRQKHLCFVKEELYPSWSVEVVAEWYWVKITNSGEFVFPLDSPHKKPYECLVLG RVKEKTPLALRNPDVRIPPVPDQKLIVSVPCVLHSHKPPLTGYLNSSFATLIPRVSNNMEYCRVVRTAFIA >XP_018079135.1 PREDICTED: methyltransferase-like protein 4 [Xenopus laevis] (SEQ ID No: 11) MSVVCETSAGWLVDELSLLRKWYQHSTSCQDAAHKKQLYDIKEDLFLILRPHIPVQSTPAPLPILCPETNPGTINQR KKRKRSCAFNQGELDAMEYHKKIIDFIMEGTQPLLQEGFKRLFLRPVLVNDDDHSQTEPRLCNNPCQLAELCNMAK CMPLLNPGEHAVQVLERGIYLPQETNVLSCITENKSECPEVIQFMGEKYIIPPKSTFLMSDVSCMEPLLHYKRYNIIVM DPPWENKSVKRSKRYSSLSPNEIQQLPVPVLAAPDCLVITWVTNKQKHLRFVKEDLYPHWSVKTLGEWHWVKITR SGEFVFPLDSTHKKPYEVLIIGRFKGAGNSTARKSEICLPPIPERKLIVSVPCKLHSHKPPLSEILKEYVKPDLECLELF ARNLQPGWTSWGNEVLKFQHIDYFTPVDVED >NP_650573.1 uncharacterized protein Dmel_CG14906 [Drosophila melanogaster] (SEQ ID No: 12) MLKLQKKTEDSKFAVFLDHKTLINEAYDEFKLKSELFQFHAKKTDKGIEEDKTRKRKRKAGVEDASSLEDLHLVNEY LELLSKPVEPEDSSPMKRHWEDGYNVPQLHGANESGRMQRFLRVDGSRGVYLIPNQSRFFNHNVDNLPALLHQLL PAYDLIVLDPPWRNKYIRRLKRAKPELGYSMLSNEQLSHIPLSKLTHPRSLVAIWCTNSTLHQLALEQQLLPSWNLR LLHKLRWYKLSTDHELIAPPQSDLTQKQPYEMLYVACRSDASENYGKDIQQTELIFSVPSIVHSHKPPLLSWLREHLL LDKDQLEPNCLELFARYLHPHFTSIGLEVLKLMDERLYEVRKVEHCNQEEVN >tr|A8J2E1|A8J2E1_CHLRE Predicted protein OS = Chlamydomonas reinhardtii OX = 3055 GN = CHLREDRAFT_174824 PE = 3 SV = 1 (SEQ ID No: 13) MATLPGAAAAAPGANAEVGVPEPSLEPQDALQQRIALAEGLLALNEADAMQAWQQLPREALLEQVAKYRGAVRD MASALRSSTLPGGVPPHCVPIHANVTTFDWPSLYSHAQFDVIMMDPPWQLATANPTRGVALGYSQLNDDHISRLP VPQLQRQGGYLFVWVINAKYKWTLDLFDRWGYRLVDEVVWVKMTVNRRLAKSHGYYLQHAKEVCLVAKRGNPP VPPGCEGGVGSDIIFSERRGQSQKPEEIYHLIEQLVPNGRYLEIFARKNNLRNYWVSIGNEVTGTGLPDEDMQALRD LHHIPGAVYGKNAPHLVSKLFLYAPNSSREEG >XP_021880122.1 MT-A70-domain-containing protein [Lobosporangium transversale] (SEQ ID No: 14) MLDQINIDIEQLEASLDIDEGKAHSNNASGTGCLIGTGTSSGNASNGAGVADEDLEEEVDDLEEFEAPEWCVPIKAN VMTYDWDSLAAECQFDVILMDPPWQLATHAPTRGVAIAYQQLPDICIEELPVPKLSSNGFIFIWVINNKYAKAFDLM RRWGYSYVDDITWVKQTVNRRMAKGHGYYLQHAKETCLVGKKGEDPPGCRHSIGSDVIFSERRGQSQKPEELYE LIEELVPNGRYLEIFGRKNNLRDYWVTVGNEL >ORX69627.1 MT-A70-domain-containing protein [Linderina pennispora] (SEQ ID No: 15) MDVDSSSPAVVLQALRQREQKIRSRILVLEQEISDLEKRCGVEGSGDAANKVTEADLEEFKAPEWSVPIRANVMNF DWEKLAQACQFDVILMDPPWQLASQAPTRGVAIAYQQLPDVCIESLPIDLLQTSGFIFIWVINNKYTKAFQLMKQWG YKYVDDIAWVKQTVNRRMAKGHGYYLQHAKETCLVGKKGPDPPNLRRSVASDVIFSERRGQSQKPEELYEIIEQLV PGGRYLEIFGRKNNLRDYWVTVGNEL >ORX98979.1 allantoinase [Basidiobolus meristosporus CBS 931.73] (SEQ ID No: 16) MSAIIFTGNRVLFDSTSKVEPATIHVDPWTGRIVKITNKRSTKADFPGIEDKDFVDAGDDLIMPGVIDAHVHLNEPGR TDWEGFDTATRAAAAGGLTTVIDMPLNSIPPTTTLENLNTKKEAAKPQAWVDVGFYGGVIPGNADQLRPMIAAGVC GFKCFLIESGVDEFPCVNEEEVRKAFAEFDGTDNVFMFHAEMECDDHSHETAAPQSTDPSAYQTFLQSRPHALEV KAIEMIIRVCKDFPNVRAHIVHLSSAEALPMIRKAKAEGVKLTVETCYHYLTLNAEDIINGATHFKCCPPIREGSNRELL WEALLDGTIDYVVSDHSPCTPELKRFDSGDFTAAWGGISSLQFGLSLLWTEAKRRGCTLQDLTRWLSQNTARHAG ILNRKGRLQIGSDADIVIWSPEETFVVDKKMIHFKNKVTPYENMTLHGAVKKTFVRGRNVYDKSTAQLFSAKPLGNL LARFQVYSNPITAMPSYAQPPSSDNGDFEEESEDYIESDEVDEDLRELLAKETSLRLRIDSLKEEILKLEREQRGETD GSKNEGEGGEEEIDLEEFEAPEWCVPIKANVMTFEWKRLAEAAQFDVILMDPPWQLATHAPTRGVAIGYQQLPDV CIEELPIPLLQKNGFIFIWVINNKYVKAFELMAKWGYRYVDDITWVKQTVNRRMAKGHGYYLQHAKETCLIGKKGED PPNCRHSVCSDVIFSERRGQSQKPEELYEMIEQLVPNGKYLEIFGRKNNLRDYWVTIGNEL >ORZ00623.1 MT-A70-domain-containing protein [Syncephalastrum racemosum] (SEQ ID No: 17) MSSREESPSSVSGFDLDTIDESTVTDTTLKNLLRREIELQLQIDALQTEILQIEESTAAGKNNKNDEELDPQDLEEFEA PEWCVPIKANVMTFDWEALASEVQFDVIVADPPWQLATHAPTRGVAIGYQQLPDVCIEEIPIQKLQKNGFIFIWVINN KYAKAFELMERWGYHYVDDITWVKQTVNRRMAKGHGYYLQHAKETCLVGKKGEDPPNCRHSVGSDVIFSERRG QSQKPEELYELIEELVPNGKYLEIFGRKNNLRDYWVTVGNEL >ORZ06213.1 MT-A70-domain-containing protein [Absidia repens] (SEQ ID No: 18) MTSDTSAMTADVLNRKRKRSPAMNGDDLSNNSDEADNNTTTGTTTSVDSNENDYQEQDREPILRLPRLNDAKLLE EVVDDVDYEDQPERYDFDFKKLWLQERGLMERIDGLLKDIARLTDFKGHYRDMVIPSDDEDDLDDEDSKAQYDAP EWCVPIKANVMTFDWESLGKEVQFDVIMADPPWQLATHAPTRGVAISYQQLPDVCIEDLPLEKLQTNGFLFIWVIN NKYAKAFEMMEKWGYKYVDDITWVKQTVNRRMAKGHGYYLQHAKETCLVGVKGTLPPYCRRSVGSDVIYSERRG QSQKPEQIYELIEEMMPGGKYLEIFGRKNNLRDYWITVGNEL >ORX43344.1 MT-A70-domain-containing protein [Hesseltinella vesiculosa] (SEQ ID No: 19) MASESNISRESSPASISSTNSESGIENVQSLTDEDLKQLILKEMNLKEHIEQLQRKISKLTANDLSTNQDSSDADDDLL NGDETMDDDSSSGSDSEVSGNEDIASVKSSPHAADKSESESESESDEGSSEDGNDEEDEFEAPKWCVPIKANVM TFDWEKLASETQFDVIVADPPWQLATHAPTRGVAIAYQQLPDVCIEDLPIEKLQTNGFIFIWVINNKYAKAFELMEKM GYTYVDDITWVKQTVNRRMAKGHGYYLQHAKETCLVGKKGVDPPSCRHSVGSDIIFSERRGQSQKPEELYELIEEL VPNGKYLEIFGRKNNLRDYWVTVGNEL >ORX52920.1 MT-A70 protein [Piromyces finnis] (SEQ ID No: 20) MMIVANEIDYEEFTAPEWCIPIKANVIDFEWDKLASECQFDAILMDPPWQLATHAPTRGVAIAYQQLPDQFIEELPIE KLQKNGFIFIWVINNKYVKAFELMKKWGYTFVDDITWVKQTVNRRMAKGHGYYLQHAKETCLVGKKGEDPVGCKH SISSDVIYSVRRGQSQKPEELYEMIEELIPNGKYLEIFGRKNNLRDYWVTIGNEL >ORX86973.1 MT-A70-domain-containing protein [Anaeromyces robustus] (SEQ ID No: 21) MDEKEVENSVLDSSNIEKSNATTSNMDVDETSNNETSTAIIKSEDGANSYDDFLKLDFTPEEEKDEVLKKLIERETEL KLKIEKEIEGIKNLELKGFSALTQKDEDVQDIDYEEFTAPEWCIPIKANVIDFEWDKLASECQFDAILMDPPWQLATHA PTRGVAIAYQQLPDQFIEELPIEKLQKNGFIFIWVINNKYVKAFELMKKWGYTFVDDITWVKQTVNRRMAKGHGYYL QHAKETCLVGKKGDDPVGCRHKISSDVIYSVRRGQSQKPEELYEMIEELIPNGKYLEIFGRKNNLRDYWVTIGNEL >XP_001032074.3 MT-a70 family protein [Tetrahymena thermophila SB210] (SEQ ID No: 22) MKKEQQFLIFKKSLIIAQKRKEINIKQLKQQFKNFLFVQIFSIIKLKLQDIIIKFKMSKAVNKKGLRPRKSDSILDHIKNKLD QEFLEDNENGEQSDEDYDQKSLNKAKKPYKKRQTQNGSELVISQQKTKAKASANNKKSAKNSQKLDEEEKIVEEE DLSPQKNGAVSEDDQQQEASTQEDDYLDRLPKSKKGLQGLLQDIEKRILHYKQLFFKEQNEIANGKRSMVPDNSIPI CSDVTKLNFQALIDAQMRHAGKMFDVIMMDPPWQLSSSQPSRGVAIAYDSLSDEKIQNMPIQSLQQDGFIFVWAIN AKYRVTIKMIENWGYKLVDEITWVKKTVNGKIAKGHGFYLQHAKESCLIGVKGDVDNGRFKKNIASDVIFSERRGQS QKPEEIYQYINQLCPNGNYLEIFARRNNLHDNWVSIGNEL >EJY88228.1 MT-A70 family protein [Oxytricha trifallax] (SEQ ID No: 23) MNQSSQDITTQKSSNGFNPQTQPETLIQVIRKESTFIFKYRKNPYYVPPPISSQTSPNLEVETSNDLNQMSDYEGQI PNNYEINRNSTQFTNNDDQSDNDFYDNNSITTMQIDTSTAKILNNGPLEYNPDLPNKEQKLKDSQVMQNQPPTATS TNSQQRTLQELINIMPSIEDISQQCKQQQQLKIQAKANSTQSASTANAANGGKGRKRGRTVRFDQPLLGKVRQRN GDASDDEEPDEIEMLIRRLHTDILNDARNDPVEQAKKIRQARESQSDQTNSTTQLSVYERMILGSASQQSTDHQPG EFSNMFRTLEDEQIEINQNFLFDEYDSEDDSIADDKVEIASDDEQMLLQEHKKRGKKYLQDEIVKEEDFDEDDDSDE DIHMDDLENESLSFDRNNRKSHKPVCKRTREENILDADLGDEKDDEDTIFIDNLPSDEFSIRRQLQDVKSYIKQFEML FFEEEDSDKEEQLKQITNVQKHEEALQNFKDRSHLKNFWCIPLSSDVREIDWDVLIARQQEHTNGQLFDVITCDPP WQLSSANPTRGVAIAYETLNDGEILKIPWGRLQKDGFLFIWVINAKYRFALDMMGAHGYRVVDEIQWVKQTCNGKI AKGHGYYLQHAKEVCLVGCKGDPAILAKKCRSNIESDVIFSERRGQSQKPEEIYELVEALVPNGYYMEIFGRRNNLH NGWVTVGNEL >EJY79437.1 MT-A70 family protein [Oxytricha trifallax] (SEQ ID No: 24) MHLPMQIITQNMFRQGNQHSCLNRTEILRTPRLTRSTKTELQEQTHFSKLPRRNYLKLQIDMREIQSLVDKKVKESA AAQQQLSQSGIEDSAIKRSLRPRKVENYKNMLEGDEITLKTIQDEQIEVKRKKREASSQNRLEDEDEDEDMLEVGQ QIERASDDEDDDDFPISTRRSARKRTRRQDVDEDEEAIEVNQVESSDAEVEIPANDIDTESYTEGTNKRKQKLKAKK QVLDKKKNKTEGDIDKEDAVEEEETVFIDNLPNDEFEIRRMLKEVKKHIKSLEKQFFEEEDSEKEEELKQINNNSKHE EALQAFKETSHLKQFWCIPLSVNVTTLDFDLLAKSQMKQGGRLFDVITIDPPWQLSSANPTRGVAIAYDTLNDKEILN MPFEKVQTDGFLFIWVINAKYRFALEMMEKFGYKLVDEIAWVKQTVNGKIAKGHGYYLQHAKETCLVGVKGNVKGK ARYNIESDVIFSQRRGQSQKPEEIYEIAEALVPNGYYLEIFGRRNNLHNGWVTIGNEL >NP_066012.1 N6-adenosine-methyltransferase non-catalytic subunit [Homo sapiens] (SEQ ID No: 25) MDSRLQEIRERQKLRRQLLAQQLGAESADSIGAVLNSKDEQREIAETRETCRASYDTSAPNAKRKYLDEGETDEDK MEEYKDELEMQQDEENLPYEEEIYKDSSTFLKGTQSLNPHNDYCQHFVDTGHRPQNFIRDVGLADRFEEYPKLREL IRLKDELIAKSNTPPMYLQADIEAFDIRELTPKFDVILLEPPLEEYYRETGITANEKCWTWDDIMKLEIDEIAAPRSFIFL WCGSGEGLDLGRVCLRKWGYRRCEDICWIKTNKNNPGKTKTLDPKAVFQRTKEHCLMGIKGTVKRSTDGDFIHA NVDIDLIITEEPEIGNIEKPVEIFHIIEHFCLGRRRLHLFGRDSTIRPGWLTVGPTLTNSNYNAETYASYFSAPNSYLTG CTEEIERLRPKSPPPKSKSDRGGGAPRGGGRGGTSAGRGRERNRSNFRGERGGFRGGRGGAHRGGFPPR >NP_964000.2 N6-adenosine-methyltransferase non-catalytic [Mus musculus] (SEQ ID No: 26) MDSRLQEIRERQKLRRQLLAQQLGAESADSIGAVLNSKDEQREIAETRETCRASYDTSAPNSKRKCLDEGETDEDK VEEYKDELEMQQEEENLPYEEEIYKDSSTFLKGTQSLNPHNDYCQHFVDTGHRPQNFIRDVGLADRFEEYPKLRELI RLKDELIAKSNTPPMYLQADIEAFDIRELTPKFDVILLEPPLEEYYRETGITANEKCWTWDDIMKLEIDEIAAPRSFIFL WCGSGEGLDLGRVCLRKWGYRRCEDICWIKTNKNNPGKTKTLDPKAVFQRTKEHCLMGIKGTVKRSTDGDFIHA NVDIDLIITEEPEIGNIEKPVEIFHIIEHFCLGRRRLHLFGRDSTIRPGWLTVGPTLTNSNYNAETYASYFSAPNSYLTG CTEEIERLRPKSPPPKSKSDRGGGAPRGGGRGGTSAGRGRERNRSNFRGERGGFRGGRGGTHRGGFTPR >XP_003129279.3 N6-adenosine-methyltransferase subunit METTL14 [Sus scrofa] (SEQ ID No: 27) MDSRLQEIRERQKLRRQLLAQQLGAESADSIGAVLNSKDEQREIAETRETCRASYDTSTPNAKRKYQDEGETDEDK IEEYKDELEMQQEEENLPYEEEIYKDSSTFLKGTQSLNPHNDYCQHFVDTGHRPQNFIRDVGLADRFEEYPKLRELI RLKDELIAKSNTPPMYLQADIEAFDIRELTPKFDVILLEPPLEEYYRETGITANEKCWTWDDIMKLEIDEIAAPRSFIFL WCGSGEGLDLGRVCLRKWGYRRCEDICWIKTNKNNPGKTKTLDPKAVFQRTKEHCLMGIKGTVKRSTDGDFIHA NVDIDLIITEEPEIGNIEKPVEIFHIIEHFCLGRRRLHLFGRDSTIRPGWLTVGPTLTNSNYNAETYASYFSAPNSYLTG CTEEIERLRPKSPPPKSKSDRGGGAPRGGGRGGTSAGRGRERNRSNFRGERGGFRGGRGGAHRGGFPPR >XP_018099063.1 PREDICTED: N6-adenosine-methyltransferase subunit METTL14 isoform X2 [Xenopus laevis] (SEQ ID No: 28) MNSRLQEIRARQTLRRKLLAQQLGAESADSIGAVLNSKDEQREIAETRETSRASYDTSAAVSKRKLPEEGKADEEV VQECKDSVEPQKEEENLPYREEIYKDSSTFLKGTQSLNPHNDYCQHFVDTGHRPQNFIRDVGLADRFEEYPKLREL IRLKDELIAKSNTPPMYLQADLENFDLRELKSEFDVILLEPPLEEYFRETGIAANEKWWTWEDIMKLDIEGIAGSRAFV FLWCGSGEGLDFGRMCLRKWGFRRSEDICWIKTNKDNPGKTKTLDPKAIFQRTKEHCLMGIKGTVHRSTDGDFIH ANVDIDLIITEEPEIGNIEKPVEIFHIIEHFCLGRRRLHLFGRDSTIRPDQSWEERLANSGGLREKEFLVGLLLGLLLPTA TLIQRLMLLTLTLQIHLLLDAQRRSKDSVPKLHLLSQIVALGHREEEDEVEHLQVAERGAGKGTEAVLGETEGISEDV EDHIGVSLLPVDFKCF >NP_996954.1 N6-adenosine-methyltransferase non-catalytic subunit [Danio rerio] (SEQ ID No: 29) MNSRLQEIRERQKLRRQLLAQQLGAESPDSIGAVLNSKDEQKEIEETRETCRASFDISVPGAKRKCLNEGEDPEED VEEQKEDVEPQHQEESGPYEEVYKDSSTFLKGTQSLNPHNDYCQHFVDTGHRPQNFIRDGGLADRFEEYPKQRE LIRLKDELISATNTPPMYLQADPDTFDLRELKCKFDVILIEPPLEEYYRESGIIANERFWNWDDIMKLNIEEISSIRSFVF LWCGSGEGLDLGRMCLRKWGFRRCEDICWIKTNKNNPGKTKTLDPKAVFQRTKEHCLMGIKGTVRRSTDGDFIH ANVDIDLIITEEPEMGNIEKPVEIFHIIEHFCLGRRRLHLFGRDSTIRPGWLTVGPTLTNSNFNIEVYSTHFSEPNSYLS GCTEEIERLRPKSPPPKSMAERGGGAPRGGRGGPAAGRGDRGRERNRPNFRGDRGGFRGRGGPHRGFPPR >NP_609205.1 methyltransferase like 14 [Drosophila melanogaster] (SEQ ID No: 30) MSDVLKSSQERSRKRRLLLAQTLGLSSVDDLKKALGNAEDINSSRQLNSGGQREEEDGGASSSKKTPNEIIYRDSS TFLKGTQSSNPHNDYCQHFVDTGQRPQNFIRDVGLADRFEEYPKLRELIKLKDKLIQDTASAPMYLKADLKSLDVKT LGAKFDVILIEPPLEEYARAAPSVATVGGAPRVFWNWDDILNLDVGEIAAHRSFVFLWCGSSEGLDMGRNCLKKW GFRRCEDICWIRTNINKPGHSKQLEPKAVFQRTKEHCLMGIKGTVRRSTDGDFIHANVDIDLIISEEEEFGSFEKPIEI FHIIEHFCLGRRRLHLFGRDSSIRPGWLTVGPELTNSNFNSELYQTYFAEAPATGCTSRIELLRPKSPPPNSKVLRG RGRGFPRGRGRPR >NP_567348.2 Methyltransferase MT-A70 family protein [Arabidopsis thaliana] (SEQ ID No: 31) MKKKQEESSLEKLSTWYQDGEQDGGDRSEKRRMSLKASDFESSSRSGGSKSKEDNKSVVDVEHQDRDSKRERD GRERTHGSSSDSSKRKRWDEAGGLVNDGDHKSSKLSDSRHDSGGERVSVSNEHGESRRDLKSDRSLKTSSRDE KSKSRGVKDDDRGSPLKKTSGKDGSEVVREVGRSNRSKTPDADYEKEKYSRKDERSRGRDDGWSDRDRDQEGL KDNWKRRHSSSGDKDQKDGDLLYDRGREREFPRQGRERSEGERSHGRLGGRKDGNRGEAVKALSSGGVSNEN YDVIEIQTKPHDYVRGESGPNFARMTESGQQPPKKPSNNEEEWAHNQEGRQRSETFGFGSYGEDSRDEAGEASS DYSGAKARNQRGSTPGRTNFVQTPNRGYQTPQGTRGNRPLRGGKGRPAGGRENQQGAIPMPIMGSPFANLGMP PPSPIHSLTPGMSPIPGTSVTPVFMPPFAPTLIWPGARGVDGNMLPVPPVLSPLPPGPSGPRFPSIGTPPNPNMFFT PPGSDRGGPPNFPGSNISGQMGRGMPSDKTSGGWVPPRGGGPPGKAPSRGEQNDYSQNFVDTGMRPQNFIRE LELTNVEDYPKLRELIQKKDEIVSNSASAPMYLKGDLHEVELSPELFGTKFDVILVDPPWEEYVHRAPGVSDSMEYW TFEDIINLKIEAIADTPSFLFLWVGDGVGLEQGRQCLKKWGFRRCEDICWVKTNKSNAAPTLRHDSRTVFQRSKEH CLMGIKGTVRRSTDGHIIHANIDTDVIIAEEPPYGSTQKPEDMYRIIEHFALGRRRLELFGEDHNIRAGWLTVGKGLSS SNFEPQAYVRNFADKEGKVWLGGGGRNPPPDAPHLVVTTPDIESLRPKSPMKNQQQQSYPSSLASANSSNRRTT GNSPQANPNVVVLHQEASGSNFSVPTTPHWVPPTAPAAAGPPPMDSFRVPEGGNNTRPPDDKSFDMYGFN >PNW88915.1 hypothetical protein CHLRE_01g050600v5 [Chlamydomonas reinhardtii] (SEQ ID No: 32) MQDGQGPPGDGRGRGRGRSRGGRIMFAREGGRGPRPMHSDMGPPPPPMGMFPHDPSAMMGGPMPGMPPM DFTPEMLLTMMGAGLGGPMGLAGPMGMMMPDFGAAAAGAPGGMMVPPGAMMPPPPQPPSGGPGGMGGGGM GGMGGMMGHQQGMGGAGGPMGLPGGGMGMGMGGGGGGGGGGGYGGRGGHGEAGGGGGGGGRAGGAG GGGGAGGAAEHLSNDYSQNFVDTGLRPQNFLRDTHLTDRYEEYPKLKELIVRKDRQVSAHATPPLFLRTDLRSTRL SPELFGTKFDVILVDPPWEEYVRRAPGMVADPEVWSWQDIQALDIEAVADNPCFLFLWCGAEEGLEAGRVCMQK WGFRRVEDICWIKTNKEGGKGPGGGRRPYLTAANQHPESMLVHTKEHCLMGIKGSVRRATDGHIIHTNVDTDVIV SEEPELGSTRKPEEMYHIIERFCNGRRRLELFGEDHNIRNGWVTVGRSLTSSNFSAKAYADHFRNRDGSVWVQNT YGPKPPPGSVILVPTTDEIEDLRPKSPTGPHGGSSFHHSR >XP_001022374.1 MT-a70 family protein [Tetrahymena thermophila SB210] (SEQ ID No: 33) MQPQQNQNQQQQQQQQSQQQQQQNQQLPQLQQSMSSQQQQNQQQEKQIIIKRGTTSKRNDYCQNFVNTHER PQNFIMNIRPEERFIEYPKLQDLIKFKDDLIKKRNHPPVYLKADLKYYDLSKLGKFDVIMMDPPWKEYEERVQGLPIYS QYPEKFNSWDLNEIAALPIDEISDKPSFLFLWVGSDHLDQGRELFRKWGYKRCEDIVWVKTNKDKTKEYIELPHSNL LVRVKEHCLVGLRGDVKRASDSHFIHANIDTDVIVAEEPPLGSTQKPAEIYDIIERFCLGRKRLELFGEVHNVRQGWL TIGKLLDESNFNQDEYNSWFDGDKTYPQIQTYRGGRYVGTTPDIEQLRPKSPTKNNQMNSNQNMSGSQVSEFDL GIQQKQQKLNQQF >NP_009876.1 Kar4p [Saccharomyces cerevisiae S288C] (SEQ ID No: 34) MAFQDPTYDQNKSRHINNSHLQGPNQETIEMKSKHVSFKPSRDFHTNDYSNNYIHGKSLPQQHVTNIENRVDGYP KLQKLFQAKAKQINQFATTPFGCKIGIDSIVPTLNHWIQNENLTFDVVMIGCLTENQFIYPILTQLPLDRLISKPGFLFI WANSQKINELTKLLNNEIWAKKFRRSEELVFVPIDKKSPFYPGLDQDDETLMEKMQWHCWMCITGTVRRSTDGHLI HCNVDTDLSIETKDTTNGAVPSHLYRIAENFSTATRRLHIIPARTGYETPVKVRPGWVIVSPDVMLDNFSPKRYKEEI ANLGSNIPLKNEIELLRPRSPVQKAQ >XP_001691478.1 predicted protein [Chlamydomonas reinhardtii] (SEQ ID No: 35) MRLGGGPGGSELDDLLGKRSVKEKVKVEKGSELLDILSKPTARESARVEQFRTAGGSAIREHCPHLTKDECRRVN GVPLACHRLHFLRVVQPHTDVALGNCSYLDTCRNMRTCKYVHYRPDPEPDVPGMGSEMARLRASVPKKPVGDG QTSRGALDPQWINCDVRSFDMTVLGKFGVIMADPPWEIHQDLPYGTMKDDEMVNLNVGCLQDNGVLFLWVTGRA MELARECMAKWGYKRVDELIWVKTNQLQRLIRTGRTGHWLNHSKEHCLVGIKGSPQLNRYVDTDVVVAEVRETS RKPDEMYSLLERLSPGTRKLEIFARVHNCKPGWVGLGNQLKNVNLIEPEVRQRFAARYGFEPDASKDCFVN >NP_192814.1 mRNAadenosine methylase [Arabidopsis thaliana] (SEQ ID No: 36) METESDDATITVVKDMRVRLENRIRTQHDAHLDLLSSLQSIVPDIVPSLDLSLKLISSFTNRPFVATPPLPEPKVEKKH HPIVKLGTQLQQLHGHDSKSMLVDSNQRDAEADGSSGSPMALVRAMVAECLLQRVPFSPTDSSTVLRKLENDQNA RPAEKAALRDLGGECGPILAVETALKSMAEENGSVELEEFEVSGKPRIMVLAIDRTRLLKELPESFQGNNESNRVVE TPNSIENATVSGGGFGVSGSGNFPRPEMWGGDPNMGFRPMMNAPRGMQMMGMHHPMGIMGRPPPFPLPLPLP VPSNQKLRSEEEDLKDVEALLSKKSFKEKQQSRTGEELLDLIHRPTAKEAATAAKFKSKGGSQVKYYCRYLTKEDC RLQSGSHIACNKRHFRRLIASHTDVSLGDCSFLDTCRHMKTCKYVHYELDMADAMMAGPDKALKPLRADYCSEAE LGEAQWINCDIRSFRMDILGTFGVVMADPPWDIHMELPYGTMADDEMRTLNVPSLQTDGLIFLWVTGRAMELGRE CLELWGYKRVEEIIWVKTNQLQRIIRTGRTGHWLNHSKEHCLVGIKGNPEVNRNIDTDVIVAEVRETSRKPDEMYA MLERIMPRARKLELFARMHNAHAGWLSLGNQLNGVRLINEGLRARFKASYPEIDVQPPSPPRASAMETDNEPMAID SITA >EAS00013.2 N6-adenosine-methyltransferase 70 kDa subunit [Tetrahymena thermophila SB210] (SEQ ID No: 37) MGSSVKDQEISNKKHKARNSSSGANNNSNSSNYQSSKRDIHQDRSYSKDDSQSRQYNSNNGGGGSSSKNSNRN SSQQGYNQNSSSNQGQNSEYGGSGSGKNSQANSQRNSSQQGLQQLNQQQQSQQQQQQMLQNQMNSMGMM NQFQNSFGLMGMQPSQPLQLLNPSMIIPSGKKQKYDFLEFPPSSQHEFRAILLDYFLSDLFDYPMHSAELFENFIEA FSDIKDSSSFIKKLELIPLLQELNDKKAIKLETCAVGTKLFDFIVDINKDKIKQLSREFSKDRPKFMPILDKKPQPSSSKT NSSSTTAPPKQAISKREIEDLLKKETGLQKEVITQSKEKSNLLNKISAAEESALAIFRKQGSRRIDYCDCGTRDKCIQIR NSTVPCNKAHFRKIIRPHTDENLGNCSYLDTCRHMDYCKFVHYELDVDINNMNNDNLLLDGIEKKLNPQWINCDLR QIDFNILGKFNCIMADPPWDIHMTLPYGTLKDREMKAMRVDLLQEEGVIFLWVTGRAMELGRECLTNWGYRRVEEI IWVKTNQLQRIIRTGRTGHWLNHSKEHCLVGIKGNPKINRKIDCDVIVSEVRETSRKPDEIYNLIERMCPGGKKIELFG RPHNTMPGWLTLGNQLPGIYLEDEEIIERYMDAYPDQDISRETMERNRIRMKNENDIDHIYNSHIQNIPPFKTKQLTK DLQLQQQSSSMQTTQQQSSSQMMPQMQQQQSSQSINSNTDLQMHGNGLYEQE >ORX92345.1 MT-A70-domain-containing protein [Basidiobolus meristosporus CBS 931.73] (SEQ ID No: 38) MKLERALFKMADMWGYNTIGIKREYDNDKSAISVIYFDPRNLRNVQHIEKTLEDICDVDSIDPDIFLDKTTSAQVPSTY IPNEEARFSEDAEIEKLLSKPSFLEMEAFSSLIGVTELIERKTFREQEAEEMFKAQGNGGFREFCEYLIKEDCKKMNT SGQPCAMTASILLTNMKLHFRRIMRPQTDLELGDCSYLNTCHRMDTCKYVHYELDDFEHPSSANITKTTIPTSLIFRP PKKVLPAQWINCDVRKFDFSILGKFSVIMADPPWDIHMTLPYGTMTDDEMKAMAIHKLQDEGLIFLWVTARAMELG RECLATWGYDRVDEVVWIKTNQLQRLIRTGRTGHWLNHSKEHCLVGIKGDPSRFNIGLACDVLVAEVRETSRKPD QIYGMIDRLSPGTRKIEIFGRQHNTRPGWFTLGNQLKDVRIVEPEVLEAYNQRYPECPAQLSAIPES >AJR96662.1 Ime4p [Saccharomyces cerevisiae YJM1248] (SEQ ID No: 39) MINDKLVHFLIQNYDDILRAPLSGQLKDVYSLYISGGYDDEMQKLRNDKDEVLQFEQFWNDLQDIIFATPQSIQFDQN LLVADRPEKIVYLDVFSLKILYNKFHAFYYTLKSSSSSCEEKVSSLTTKPEADSEKDQLLGRLLGVLNWDVNVSNQGL PREQLSNRLQNLLREKPSSFQLAKERAKYTTEVIEYIPICSDYSHASLLSTAVYIVNNKIVSLQWSKISACQENHPGLI ECIQSKIHFIPNIKPQTDISLGDCSYLDTCHKLNMCRYIHYLQYIPSCLQERADRETAIENKRIRSNVSIPFYTLGNCSA HCIKKALPAQWIRCDVRKFDFRVLGKFSVVIADPAWNIHMNLPYGTCNDIELLGLPLHELQDEGIIFLWVTGRAIELG KESLNNWGYNVINEVSWIKTNQLGRTIVTGRTGHWLNHSKEHLLVGLKGNPKWINKHIDVDLIVSMTRETSRKPDE LYGIAERLAGTHARKLEIFGRDHNTRPGWFTIGNQLTGNCIYEMDVERKYQEFMKSKTGTSHTGTKKIDKKQPSKL QQQHQQQYWNNMDMGSGKYYAEAKQNPMNQKHTPFESKQQQKQQFQTLNNLYFAQ >NP_651204.1 methyltransferase like 3 [Drosophila melanogaster] (SEQ ID No: 40) MADAWDIKSLKTKRNTLREKLEKRKKERIEILSDIQEDLTNPKKELVEADLEVQKEVLQALSSCSLALPIVSTQVVEKI AGSSLEMVNFILGKLANQGAIVIRNVTIGTEAGCEIISVQPKELKEILEDTNDTCQQKEEEAKRKLEVDDVDQPQEKTI KLESTVARKESTSLDAPDDIMMLLSMPSTREKQSKQVGEEILELLTKPTAKERSVAEKFKSHGGAQVMEFCSHGTK VECLKAQQATAEMAAKKKQERRDEKELRPDVDAGENVTGKVPKTESAAEDGEIIAEVINNCEAESQESTDGSDTCS SETTDKCTKLHFKKIIQAHTDESLGDCSFLNTCFHMATCKYVHYEVDTLPHINTNKPTDVKTKLSLKRSVDSSCTLYP PQWIQCDLRFLDMTVLGKFAVVMADPPWDIHMELPYGTMSDDEMRALGVPALQDDGLIFLWVTGRAMELGRDCL KLWGYERVDELIWVKTNQLQRIIRTGRTGHWLNHGKEHCLVGMKGNPTNLNRGLDCDVIVAEVRATSHKPDEIYGI IERLSPGTRKIELFGRPHNIQPNWITLGNQLDGIRLVDPELITQFQKRYPDGNCMSPASANAASINGIQK >NP_001084701.1 methyltransferase like 3 L homeolog [Xenopus laevis] (SEQ ID No: 41) MSDTWSSIQAHKKQLDNLRERLQRRRKDATSQLALDLQSSEGGIAPTFRSDSPVPSASSQPLKGPSGSAEVTPDP ELEKKLLHHLSDLSLVLPADSVSIQLAITTPDFPVTRQGVESLLQKFAAQELIEVKGWGQEDDDRPTVVTFADYSKLS AMMGAVAERKGTTIPTGAKKRRLQEADPSASSLSSSLSASASREKKTSEPQKKARKHASHLDLEIESLLSQQSTKE QQSKKVSQEILELLSTSTAKEQSIVEKFRSRGRAQVQEFCDFGTKEECMKAAGADTPCRKLHFRRIINMHTDESLG DCSFLNTCFHMDTCKYVHYEIDAWVEPGGTAMGTEAIASLDTPLAKAVGDSSVGRLFPAQWIRCDIRYLDVSILGKF SVVMADPPWDIHMELPYGTLTDDEMRKLQIPVLQDDGFLFLWVTGRAMELGRECLKLWGYERVDEIIWVKTNQLQ RIIRTGRTGHWLNHGKEHCLVGVKGSPQGFNRGLDCDVIVAEVRSTSHKPDEIYGMIERLSPGTRKIELFGRPHNIQ PNWITLGNQLDGIHLLDPDVVAQFKQKYPDGVIGMPKNM sp|F1R777.1|MTA70_DANRE RecName: Full = N6-adenosine-methyltransferase subunit METTL3: AltName: Full = N6-adenosine-methyltransferase 70 kDa subunit; Short = MT-A70  (SEQ ID No: 416) MSDTWSHIQAHKKQLDSLRERLQRRRKDPTQLGTEVGSVESGSARSDSPGPAIQSPPQVEVEHPPDPELEKRLLG YLSELSLSLPTDSLTITNQLNTSESPVSHSCIQSLLLKFSAQELIEVRQPSITSSSSSTLVTSVDHTKLWAMIGSAGQS QRTAVKRKADDITHQKRALGSSPSIQAPPSPPRKSSVSLATASISQLTASSGGGGGGADKKGRSNKVQASHLDMEI ESLLSQQSTKEQQSKKVSQEILELLNTSSAKEQSIVEKFRSRGRAQVQEFCDYGTKEECVQSGDTPQPCTKLHFRR IINKHTDESLGDCSFLNTCFHMDTCKYVHYEIDSPPEAEGDALGPQAGAAELGLHSTVGDSNVGKLFPSQWICCDIR YLDVSILGKFAVVMADPPWDIHMELPYGTLTDDEMRKLNIPILQDDGFLFLWVTGRAMELGRECLSLWGYDRVDEII WVKTNQLQRIIRTGRTGHWLNHGKEHCLVGVKGNPQGFNRGLDCDVIVAEVRSTSHKPDEIYGMIERLSPGTRKIE LFGRPHNVQPNWITLGNQLDGIHLLDPEVVARFKKRYPDGVISKPKNM >NP_062826.2 N6-adenosine-methyltransferase catalytic subunit [Homo sapiens] (SEQ ID No: 42) MSDTWSSIQAHKKQLDSLRERLQRRRKQDSGHLDLRNPEAALSPTFRSDSPVPTAPTSGGPKPSTASAVPELATD PELEKKLLHHLSDLALTLPTDAVSICLAISTPDAPATQDGVESLLQKFAAQELIEVKRGLLQDDAHPTLVTYADHSKLS AMMGAVAEKKGPGEVAGTVTGQKRRAEQDSTTVAAFASSLVSGLNSSASEPAKEPAKKSRKHAASDVDLEIESLL NQQSTKEQQSKKVSQEILELLNTTTAKEQSIVEKFRSRGRAQVQEFCDYGTKEECMKASDADRPCRKLHFRRIINK HTDESLGDCSFLNTCFHMDTCKYVHYEIDACMDSEAPGSKDHTPSQELALTQSVGGDSSADRLFPPQWICCDRY LDVSILGKFAVVMADPPWDIHMELPYGTLTDDEMRRLNIPVLQDDGFLFLWVTGRAMELGRECLNLWGYERVDEII WVKTNQLQRIIRTGRTGHWLNHGKEHCLVGVKGNPQGFNQGLDCDVIVAEVRSTSHKPDEIYGMIERLSPGTRKIE LFGRPHNVQPNWITLGNQLDGIHLLDPDVVARFKQRYPDGIISKPKNL >sp|Q8C3P7.2|MTA70_MOUSE RecName: Full = N6-adenosine-methyltransferase subunit METTL3; AltName: Full = Methyltransferase-like protein 3; AltName: Full = N6-adenosine- methyltransferase 70 kDa subunit; Short = MT-A70 (SEQ ID No: 43) MSDTWSSIQAHKKQLDSLRERLQRRRKQDSGHLDLRNPEAALSPTFRSDSPVPTAPTSSGPKPSTTSVAPELATD PELEKKLLHHLSDLALTLPTDAVSIRLAISTPDAPATQDGVESLLQKFAAQELIEVKRGLLQDDAHPTLVTYADHSKLS AMMGAVADKKGLGEVAGTIAGQKRRAEQDLTTVTTFASSLASGLASSASEPAKEPAKKSRKHAASDVDLEIESLLN QQSTKEQQSKKVSQEILELLNTTTAKEQSIVEKFRSRGRAQVQEFCDYGTKEECMKASDADRPCRKLHFRRIINKH TDESLGDCSFLNTCFHMDTCKYVHYEIDACVDSESPGSKEHMPSQELALTQSVGGDSSADRLFPPQWICCDIRYL DVSILGKFAVVMADPPWDIHMELPYGTLTDDEMRRLNIPVLQDDGFLFLWVTGRAMELGRECLNLWGYERVDEIIW VKTNQLQRIIRTGRTGHWLNHGKEHCLVGVKGNPQGFNQGLDCDVIVAEVRSTSHKPDEIYGMIERLSPGTRKIEL FGRPHNVQPNWITLGNQLDGIHLLDPDVVARFKQRYPDGIISKPKNL >XP_003128628.1 N6-adenosine-methyltransferase 70 kDa subunit [Sus scrofa] (SEQ ID No: 44) MSDTTWSSIQAHKKQLDSLRERLRRRRKQDSGHLDLRNPEAALSPTFRSDSPVPTVPTSGGPKPSTASAVPELATD PELEKKLLHHLSDLALTLPTDAVSIRLAISTPDAPATQDGVESLLQKFAAQELIEVKRSLLQDDAHPTLVTYADHSKLS AMMGAVAEKKGPGEVAGTITGQKRRAEQDSTTVAAFASSLTSSLASSASEVAKEPTKKSRKHAASDVDLEIESLLN QQSTKEQQSKKVSQEILELLNTTTAKEQSIVEKFRSRGRAQVQEFCDYGTKEECMKASDADRPCRKLHFRRIINKH TDESLGDCSFLNTCFHMDTCKYVHYEIDACMDSEAPGSKDHTPSQELALTQSVGGDSNADRLFPPQWICCDIRYL DVSILGKFAVVMADPPWDIHMELPYGTLTDDEMRRLNIPVLQDDGFLFLWVTGRAMELGRECLNLWGYERVDEIIW VKTNQLQRIIRTGRTGHWLNHGKEHCLVGVKGNPQGNQGLDCDVIVAEVRSTSHKPDEIYGMIERLSPGTRKIEL FGRPHNVQPNWITLGNQLDGIHLLDPDVVARFKQRYPDGIISKPKNL >WP_009339935.1 MULTISPECIES: S-adenosylmethionine-binding protein [Afipia] (SEQ ID No: 45) MTLPAKDLLSFAGQRRFSTILADPPWQFTNKTGKVAPEHKRLSRYGTMKLDEIMMLPVADIAAPTSHLYLWCPNAL LPEGLAVMKAWGFNYKSNIVWHKVRKDGGSDGRGVGFYFRNVTEVILFGVRGKNARTLAPGRRQVNLLATRKRE HSRKPDEQYEIIESCSPGPFLELFARGTRKNWATWGNQADDDYKPTWKTYAHHSRAGLVAAE >WP_013485562.1 S-adenosylmethionine-binding protein [Ethanoligenens harbinense] (SEQ ID No: 46) MSTAKETANNLLQFCGEKKYATVYADPPWRFQNRTGKVAPENKKLNRYPTMDLEDIKALPVGKIAAEKSHLYLWVP NALLPDGLEVMKAWGFEYKGNIIWEKVRKDGEPDGRGVGFYFRNVTEILLFGIRGGNNRTLAPARSQVNLIRTQKR EHSRKPDEIITIIESCSPGPYLELFARGDRENWDMWGNQATAEYEPTWNTYKNHTTKETTSGVSGSQSET >WP_016343787.1 adenine-specific DNA methyltransferase [Mycobacteroides abscessus] (SEQ ID No: 47) MAAPLREVNEPPPLPVTDGGFSTILADPPWRFTNRTGKVAPEHRRLDRYSTLSLDEICALGVSDVTADNAHLYLWV PNALLPDGLRVMEEWGFRYVSNIVWSKVRRDGLPDGRGVGFYFRNTTELLLFGVRGSMRTLQPARSQVNQIVTR KREHSRKPDEQYELIEACSPGPYLEMFGRYRRPNWAVWGDEANEDVEPRGQTHKGYGGGEITRLPALEPHSRIP QWLAKPIAAAIKSAYDDGMSIDAIAAETGYSISRVRHLLDQAGAKKRGRGRPAKA >WP_023133224.1 MULTISPECIES: MT-A70 protein [Rothia]  (SEQ ID No: 48) MLDPMNTNEEFAPLPTVEGGFQTVLADPPWRFTNRTGKVAPEHHRLGRYGTMSLDEIKALRVGDVTADNAHLYL WVPNALLPEGLEVMQAWGFRYVSNIIWAKRRKDGGPDGRGVGFYFRNVTEPILFGVKGSMRTLAPGRSTVNMIET RKREHSRKPDEQYDLIEACSPGPYLELFARYARPGWSVWGNEASNEIEPRGKAQKGYGGGEIDRLPILEPNERMS EWLSGRVGELLAEEYTKGASVQELANQSGYSIARVRTLLTHSGVPLRGRGRPKKGQVAS >ETW92643.1 S-adenosylmethionine-binding protein [Candidatus Entotheonella factor]  (SEQ ID No: 49) MSNSPHSAADDLLACGFPPHSFSTVLADPPWRFTNRTGKMAPEHRRLSRYPTLTLEEIADLPLAQLVQPDSHLYLW VPNALLAEGLDVMRRWGFTYKTNLVWYKIRRDGGPDRRGVGFYFRNVTELVLFGVRGRMRTLAPGRRQENLLAS QKQEHSRKPDTFYDLIERCSPGPYLELFARHPRPGWHQFGNEPLVSSS >AHJ63281.1 Adenine-specific methyltransferase [Granulibacter bethesdensis] (SEQ ID No: 50) MTKQPDPIAEFRNQLNGGNFATVLADPPWRFQNRTGKMAPEHRRLSRYGTMELPEIMALPVSEVTAKTAHLYLWV PNALLPEGLAVMQAWGFNYKSNLVWHKIRKDGGSDGRGVGFYFRNVTELVLFGVKGKNARTEAPGRRQVNLLAT QKREHSRKPDEFYDIVEACSPGPYLELFARGTRPGWCAWGNQAEEYDITWDTYSHHSQRQSLWVAE >WP_017364718.1 S-adenosylmethionine-binding protein [Methylococcus capsulatus] (SEQ ID No: 51) MTENTLDPAADLLERLGDKRFRTILADPPWQFQNRTGKMAPEHKRLNRYGTMSLEAIAGLPVERLTADTAHLYLWV PNALLLEGLKVMEAWGFTYKTNLVWHKIRKDGGPDGRGVGFYFRNVTELVLFGVRGKNARTLAAGRRQVNFLAT RKREHSRKPDEMYGIIEACSPGPYLELFARGARDRWSVWGNEADENYYPRWNTYANHSQAEICPFE >WP_027700599.1 S-adenosylmethionine-binding protein [Xylella fastidiosa] (SEQ ID No: 52) MTKHKANTASDVGRDLLARHGGQRFHTILADPPWQFQNRTGKMAPEHKRLSRYGTMTLDDIMMLPVEQLVTDTA HLYLWVPNALLPEGIKVLEAWGFSYKSNIVWHKVRKDGGPDGRGVGFYFRNVTELVLFGVRGKNARTLAPGRRQ VNFLATQKREHSRKPDEFYDIVESCSPGPFLELFARGPRDGWKVWGNQADKYYPTWPTYSNHSQAECELGRVE MIAQRLLSV >WP_027488351.1 S-adenosylmethionine-binding protein [Rhizobium undicola] (SEQ ID No: 53) MLNRNTDAPSPSDDFTNFISGRKFATIMADPPWQFMNRTGKVAPEHKRLNRYGTMELDAIKALPVATACAPTAHLY LWVPNALLPEGLEVMKAWGFNYKANIVWHKLRKDGGSDGRGVGFYFRNVTELILFGTRGKNARTLPPGRSQVNYI GTRKREHSRKPDEQYPLIESCSPGPYLEMFGRGLRKGWTTWGNQADETYEPTWKTYGHNSSTDRLEAAE >ESK34829.1 hypothetical protein G966_02949 [Escherichia coli UMEA 3323-1] (SEQ ID No: 54) MGWFMTKKYTLIYADPPWVYRDKAADGNRGAGFKYPVMSVLDICRLPVWDLADENCLLAMWWVPTQPLEALKVV EAWGFRLMTMKGFTWIKCGSRQPDKLVMGMGHMTRANSEDCLFAVKGKLPTRINAGIVQSFTAPRLEHSRKPDIV REKLVQLLGDVSRIELFARQTSHGFDVWGNQCEDPAVQLHPGYALDIGGLTNAFSNAPLSPTDIQGRERAA >AIF94871.1 Adenine DNA methyltransferase, phage-associated [Escherichia coli O157:H7 str. SS17] (SEQ ID No: 55) MTKKYTLIYADPPWTFRDKATDGQRGASFKYPVMSLLDICRLPVWELAADNCLLAMWWVPTQPLEALKVVEAWG FRLVTMKGLTWNKCGKRQTDKLVMGMGSTTRANSEDCLFAVKGNLPERINAGIIQSFTAPRLDHSRKPDMAREKL VQLLGDVPRIELFARHTSHGFDVWGNQCGTPSIEMVPGIVKFLEKTNERKNDVDKGITS >WP_032715146.1 adenine methylase [Klebsiella aerogenes] (SEQ ID No: 56) MTGKYTLIYADPPWSYRDKAADGDRGAGFKYPVMNVMDICRLPVWELSADDCLLAMWWVPTQPVEALKVVEAW GFRLMTMKGFTWHKINKHKGNSAIGMGHMTRANSEDCLFAVRGKLPERMDASICQHVTAPRLENSRKPDVIREKL VQLLGDVPRIELFARQSSHGFDVWGNQCIAPAVELLPGCAVPVVKTEAA >AIA43360.1 DNA methyltransferase [Klebsiella pneumoniae subsp. pneumoniae KPNIH27] (SEQ ID No: 57) MNYDLIYCDPPWEYGNRISNGAACNHYSTMSIDDLKFLPVRKLAADNAVLAMWYTGTHNREAVELAESWGFRVRT MKGFTWVKLNQNAADRFNKALSTGELVDFNDLLEMLDRETRMNGGNHTRSNTEDVLIATRGTGLPRASASVKQV VHTCLGEHSAKPWEVRNRLEQLYGDVKRIELFAREEWKGWDRWGNQCNNSIEIITGLIKEVNHAA >WP_009320301.1 DNA methyltransferase [Clostridioides difficile] (SEQ ID No: 58) MPAVLFLLELHRRRKGGYKIENNQKYNIIYADPPWRYQQKRLSGAAEHHYPTMSVKDICGLKVEEIAAKDCVLFLWA TFPQLPEALRVIKAWGFQYKTVAFVWLKQNKSGKGWFFGLGFWTRGNAEICLLAIKGKPHRNSNRVHQFLISPIRG HSQKPEEAREKIVELMGDLPRVELFAREKTEGWDAWGNEVESDIEISSDTEKEWR >WP_012115592.1 MT-A70 family protein [Xanthobacter autotrophicus] (SEQ ID No: 59) MNGLWQFGDLKMFGYDLIVADPPWDFELYSEAGEGKSAKAHYGTMKLDEIAALRVGDLARGDCLLLLWCCEWMP PAARQRVLDAWGFTYKTTIIWRKVTRAGKVRMGPGYRARTMHEPVIVATVGNPKHTPFSSVFDGVAREHSRKPEA FYRMVEAAAPKAARADLFSRQRRDGWDAFGNEVEKFDQPPAEAAE >KFL31466.1 DNA methyltransferase [Devosia riboflavina] (SEQ ID No: 60) MTAWPFGAMPMFSFDVVMADPPWSFDNWSEGGNAKNAKAQYDCMPTPDIKRLPVGHLAAGDCWLWLWATYP MLPDAIEVMDAWGFRYVTAGPWVKRGTSGKLAMGTGYVLRSCSEIFLIGKNGEPKTHARDVRNVLEAPRREHSRK PDEAYAMAEKLFGPGRRADLFSRETRPGWTSWGNESTKFDEVAA >WP_016734162.1 DNA methyltransferase [Rhizobium phaseoli] (SEQ ID No: 61) MRLFPDLWPFGDLQPHSFDFIMADPPWKMQEWSDNGDKSKSTQSKYRLMPLDEIKAMPVLDLAAPNCLLWLWAT NPMLPQALDVLHAWGFTFATAGSWMKTTRNGKQAFGTGYIFRTSNEPILIGKRGEPKTTRSVRSSFPGLAREHSR KPEEGYREAERLMPRARRLELFSRTNRVGWTTWGDEVGKFGDVA >KFB10357.1 Adenine-specific methyltransferase [Nitratireductor basaltis] (SEQ ID No: 62) MHLFDWPFGDLNPHSFDLIMADPPWAFELRSDKGEGKSAQSHYKCQTLDEIKALPVLDLAAPDCLLWLWATNPML PQAFEVMAAWGFTFKTAGAWGKTTVNGKLAFGTGYIFRSAHEPILIGTRGEPRTTKSVRSLIMGQVREHSRKPEEA YAAAEKLIPNARRLELFSRTDRAGWEVWGDEAGKFGEAA Protein sequences for phylogenetic analysis of p1 proteins >XP_001009903.1 [Tetrahymena thermophila SB210] (SEQ ID No: 63) MSLKKGKFQHNQSKSLWNYTLSPGWREEEVKILKSALQLFGIGKWKKIMESGCLPGKSIGQIY MQTQRLLGQQSLGDFMGLQIDLEAVFNQNMKKQDVLRKNNCIINTGDNPTKEERKRRIEQNR KIYGLSAKQIAEIKLPKVKKHAPQYMTLEDIENEKFTNLEILTHLYNLKAEIVRRLAEQGETIAQPS IIKSLNNLNHNLEQNQNSNSSTETKVTLEQSGKKKYKVLAIEETELQNGPIATNSQKKSINGKRK NNRKINSDSEGNEEDISLEDIDSQESEINSEEIVEDDEEDEQIEEPSKIKKRKKNPEQESEEDDI EEDQEEDELVVNEEEIFEDDDDDEDNQDSSEDDDDDED >EJY79729.1 [Oxytricha trifallax] (SEQ ID No: 64) MSSSISAAIIAGNQNKKIAESKSLWNYALSPGWTQQEVEILKIALMKFGVGRWKTIEQSQCLPT KTMSQMYLQTQRLVGQQSLAEFMGLHLDLEQIFIKNAERQGAGVFRKNGCIINTGDNMTKVQI AKLRKKNSKIFGLTQPFVQSLHLPKAKVKEWLKVLTLDQILSAKSNFSTAEKIHYLKILENALER KLKKILRLQELVSIYRPCNIGIVVQKRLGSSIGDEYFEYVDCVKIEEKSVGNLDFALPNRNTDSTS LNEDFSFLDSTQKPQKLKAGSGRENKRKKMRDGLKDERAQRQSLMEALDEQEFDETKFQDS >EJY78001.1 [Oxytricha trifallax] (SEQ ID No: 65) MSVHHKMADSKSLHNYTLSPGWTREEVDILKIALMKFGIGKWKKIQKSGCLPSKTISQMNLQT QRLLGQQSLAEFMGLHVYLDRVFRDNSLKTGPEIQRKNNFIINTGNNLTQPEKEKRLRLNKQK YGLDLAFIKTLRLPKPESATGGKREAILSMDQIFAQKSHFTVVEKLKHLEALKNALCSKLGKIER RRRNKELSKIYRPLGQLIVVQKNADDQYEFVDIIDENE >ORX69504.1 [Linderina pennispora] (SEQ ID No: 66) MSSATPYAPRSMPTGQRNVVRSNDSASLWNCTLSPGWTQEEVQVLRKALMKFGVGNWMKII ESECLPGKTIAQMNLQTQRMLGQQSTAEFNGLHLDAFVIGELNSKKQGPGIKRKNNCIVNTGG KLTRDEVVKRQQKHREQYEVKAEVWRAIVLPKPDNPLILLEKKREELKKVRLELEEIMKQIEET >ORX78557.1 [Basidiobolus meristosporus CBS 931.73] (SEQ ID No: 67) MTDVYKPRSMPVGARNVLRSNDSASLWNCTLSPGWTEPEVHILRKAVMKFGIGNWAKIIESQ CLFGKTIAQMNLQLQRMLGQQSTAEFAGLHLDPFVIGEINSKKQGPGIKRKNNCIVNTGGKLTR EEIKRRLLEHKRTYEISEEEWRSIELPKPEDPGAVLIAKKDELKMLEDELLRVVQKIQKAREERR SKSVDSSSVDGSVDDEARETKRRRK >EJY73777.1 [Oxytricha trifallax] (SEQ ID No: 68) MSHATSHGNSTEKDKKNSGNMVAESKSLWNYALSPQWTPQEVDVLKIALMKFGIGKWTIIDK SGILPTKTIQQCYLQTQRILGQQSLAEFMGLHVDIDKIALDNRRKNGIRKMGFLVNQGGKLTPE EKAHYQEINRQKYGLSPEEVETIKLPPPCSVEIYDINKIINPKSKLTTIEKINHCIKLQDALLEKLEN IKNKKIPTGAGFSSSRVYENMRGYDPQLLLNSHVTGQLDHSMQDLTIDERYSDLDEEEDPLAM ASIIDSQATPQPQKIKSSVPNKASTTPSAKEMNQIKDIIDSVIAENSAQQSKNLAQEKPKLKFSLV KATESNLLQSAAQNSDDVVMEEDSKLQHIETFSTVTQTATDQSNSQSKSQNNIASDSLKDSLE QNDLSKSLTDSLEMQQYSAEKKLNQAPMSKNSDKPKKKRLNKRKLPSDDEFETL >XP_021883515.1 [Lobosporangium transversale] (SEQ ID No: 69) MSSGSTPRSMTAGARNILRSNDSASLWNYTVAPGWSMKEAEILRKALMKFGIGNWSKIIESN CLVGKTNAQMNLQTQRMLGQQSTAEFAGLHIDPRVIGQKNSLIQGDHIRRKNGCIVNTGAKLS REEIRRRVAENKEQYELPEEEWSSIELPLPDDPHLLLEAKKSEKVRLELELKNVQRQIAMLRKV GRKFETGSESPKTELDDDERDEFIEDQPLGKRARIEA >EJY81929.1 [Oxytricha trifallax] (SEQ ID No: 70) MSSSISAAIMAGNQNKKIAESKSLWNYALSPGWTQQEVEILKIALMKFGVGRWSAINKSGVLP TKQIQQCYLQTQRLIGQQSLAEFMGLHLDIDRIAADNKQKRGIRKQGFLVNQGCKLTPEEKDEL RKINQEKYGLSAEHVEAIKLPAPCHLVEIFQIDKIMHPRSTLSTMDKIKHLIKLEDALKSKLEMIRE GKRQQKFEQLQQKLKTTEASGRGSVTRVQRQMSDLHLGSSHQNRNSDLDEENDESVMIIDE SQQENLTPKGKAQAMLTHQKYNEVTQTMIKQGDDSRQQQHLPLDSTSASVSNPSSTSKSST MKSNSMKQSETAIASMKPSSIGKKTKVDSSFVTKQSNQQSTAPIQKQAHQQNLDRNRSELGS TFAQQASVDTQNSNNQGTSTASGNFISQSDDEEALMPKLKRRRVEDSE >EJY76686.1 [Oxytricha trifallax] (SEQ ID No: 71) MRVYLKFCNRKQIHYTHTMSSSISAAIMAGNQNKKIAESKSLWNYALSPGWTQQEVEILKIALM KFGVGRWSAINKSGVLPTKQIQQCYLQTQRLIGQQSLAEFMGLHLDIDRIAADNKQKRGIRKQ GFLVNQGCKLTPEEKDELRKINQEKYGLTAEHVEAIKLPAPCHLVEIFQIDKIMHPRSTLSTMDK IKHLIKLEDALKSKLEMIREGKRQQKFEQLQQKLKTTEASGRGSVTRVQRQMSDLHLGSAHQN RNSDLDEENDQSVMIIDESQQQNLTPKGKAQTMLTNQTQTMKKQADDSRDEQHLPLISTSAS VSNPSSTSKSSALKLNSMKQSDTAIASMKPSSSGKKTKVDSSFVSKQSNQQSTSYSETNVDT QNSNNQGTSTASGNFISQSDDEEALMPKLKRRRVEDSE >EJY80746.1 [Oxytricha trifallax] (SEQ ID No: 72) MRVYLKFCNRKQIHYTHTMSSSISAAIMAGNQNKKIAESKSLWNYALSPGWTQQEVEILKIALM KFGVGRWSAINKSGVLPTKQIQQCYLQTQRLIGQQSLAEFMGLHLDIDRIAADNKQKRGIRKQ GFLVNQGCKLTPEEKDELRKINQEKYGLTAEHVEAIKLPAPCHLVEIFQIDKIMHPRSTLSTMDK IKHLIKLEDALKSKLEMIREGKRQQKFEQLQQKLKTTEASGRGSVTRVQRQMSDLHLGSAHQN RNSDLDEENDQSVMIIDESQQQNLTPKGKAQTMLTNQTQTMKKQADDSREEQHLPLNSTSAS VSNPSSTSKSSALKLNSMKQSDTAIASMKPSSSGKKTKVDSSFVSKQSNQQSTGPIQKQAHQ QNLDRNRSELGSTFAQQTNVDTQNSNNQGTSTASGNFISQSDDEEALMPKLKRRRVKDSE >ORX56566.1 [Piromyces finnis] (SEQ ID No: 73) MSIPKPRSMPVGFRNILRPNDSTSLWNCTLSPGWTQEESDILRDALIFYGIGNWKDIIEHGCLP DKTNAQMNLQLQRMLGQQSTAEFQNLHIDPYEIGKINSQKQGPNIRRKNGFIINTGGKLSREDI KRKIQENKENYELPEEVWSKIVLPNREVVTINEKRQKLNKLEEELDSVLKQIVNRRRELRGMTP LKETEMKSIVNRSNQNDTKTEEKEIKEEESTTVNEEKIENTETSSISIISTNENEQSENISSSSPIV KSEQKKKRVVSRRKNKRRVNSDDEDFLPPGKSRSKRTRRTPKKSSN >ORX79686.1 [Anaeromyces robustus] (SEQ ID No: 74) MSIPKPRSMPTGFRNILRPNDSTSLWNCTLSPGWTQEESDILRDALIYYGIGNWKDIIEHGCLP DKTNAQMNLQLQRMLGQQSTAEFQNLHIDPYVIGKINSQKQGPNIRRKNGFIINTGGKLSREDI RRKIQENKENYELPKEEWSKIVLPNREVVIKNKVQEAINEKREKLNKLEDELDSVLKAIVNRRR ELRGMIPLKDSEMKSLVNRSAKNEGENKTETTNNEESNNTNNSDDIKDENNETSTSSHIFTNN DNELSENNSSSSSSNSISNKKKRFLRREVRRGKRRYNYDDDDFMPSGNRSRKSRKI >ORZ01404.1 [Syncephalastrum racemosum] (SEQ ID No: 75) MSNNKENNVNKPRSMTAGARNVLRSNDSTSLWNCTLSPGWTQDESEVLRKALMKFGVGNW AKIIESGCLPGKTNAQMNLQLQRLLGQQSTAEFAGLHIDPKVIGEKNSKIQGPHIKRKNNCIVNT GDKLSRDKLRARVMSNKEEYELPEEVWKNIELPKVKDPLMLLEGKKEEMRKLKTELEKVQAKI QQLRQAQPARVQELQSQIEVARSPSPSAPDSPALSV >XP_001698763.1 [Chlamydomonas reinhardtii] (SEQ ID No: 76) MAFAAALAEKRGPRVGDAASLWNFTPAPGWSREEVQILRLCLMKHGVGQWMQILSTGLLPG KLIQQLNGQTQRLLGQQSLAAYTGLKVDVDRIRVDNETRTDATRKAGLIINDGPNLTKEMKEK MRQDAVAKYGLTPEQVAEVDEQLAEIAAAFNPASTSAAAGAGSGAAAAGQAAAAGSGAGGS GNLMAQPTEQLSAEQLGQLLLRLRNRLACLVDRARGRAGLPPRTAPRWATEAAAAACLAAM AAAEASAPQAPAAAAGGQEGAAGPVMVSVPFSREVLAEATACRVRSGTAAGARGNAPGAQ GGVRKRTSKGGKAKGGDREWSPEGEENTAPQPRGGGKRKSGAVAGGEEADGVASGRAKR ASRPKRGSSKHDPYVDDNDYGDEGIDPFDVGDDLDDMNPHGRYGNGGGRRADPSEAISALT AMGFTQSKARGALRECNFNVELAVEWLFANCL >PNW76495.1 [Chlamydomonas reinhardtii] (SEQ ID No: 77) MAFAAALAEKRGPRVGDAASLWNFTPAPGWSREEVQILRLCLMKHGVGQWMQILSTGLLPG KLIQQLNGQTQRLLGQQSLAAYTGLKVDVDRIRVDNETRTDATRKAGLIINDGPNLTKEMKEK MRQDAVAKYGLTPEQVAEVDEQLAEIAAAFNPASTSAAAGAGSGAAAAGQAAAAGSGAGGS GQAATAADAGGAAGRGTGSAGGAAAAAPPRNALAISTGVLAATLLDASLGNLMAQPTEQLSA EQLGQLLLRLRNRLACLVDRARGRAGLPPRTAPRWATEAAAAACLAAMAAAEASAPQAPAAA AGGQEGAAGPVMVSVPFSREVLAEATACRVRSGTAAGARGNAPGAQGGVRKRTSKGGKAK GGDREWSPEGEENTAPQPRGGGKRKSGAVAGGEEADGVASGRAKRASRPKRGSSKHDPY VDDNDYGDEGIDPFDVGDDLDDMNPHGRYGNGGGRRADPSEAISALTAMGFTQSKARGALR ECNFNVELAVEWLFANCL >ORZ17038.1 [Absidia repens] (SEQ ID No: 78) MSSPSSPSPIKPRSMLTGSRNVVRSNDSASLWNCTLSPGWNEEQSETLRHAVMKYGIGNWA KIIDSGYLPGKTNAQMNLQLQRLLGQQSTAEFAGLHIDPKVIGEQNSRIQGPEIRRKNNTIVNTG DKLSREALRERILRNKEKYELPESVWQAIELEHVTDEDALLEEKKKTLREMKSQLKVVQRQIKN LEFMHPLHAAKLKFELEKLAPSSSTSSSSSSPSPSSSSSPSSSSSKPSVSGTEEEMREAVDEE RGSDEEIDELVEETDEEETSVSPKVGTRTKKVRTN >ORX56339.1 [Hesseltinella vesiculosa] (SEQ ID No: 79) MIANSTATPKPRSMKAGARNVLRSNDSASLWNCTLSPGWTEQESEILRQLAIKFGIGNWAKIIE SDCLPGKTNAQMNLQLQRLLGQQSTAEFAGLHIDPKVIGEKNSKIQGPHIKRKNTTIVNTGGKL SREELRERQAKNKEMYEMPKSAWDSIDLDELRDMNSLKLKKKEDKDALKKQKLTQLKTKLTK SQNNLKKVQAELKQIAMVDPERVAELKKELSRASSPLSNEVSVIEESPAKKQRTS >ORX54764.1 [Piromyces finnis] (SEQ ID No: 80) MVVEKDLAQENKIKEELNKKHEWVKEMRKKFCVRKEFENTKNLILEDGTLNQEYFRLSKGTVL KTNEVRKWTSIERNLLIKGIEKYGIGHFREISESLLPKWSGNDLRIKTIHLIGRQNLKLYKDWKG GEEDIKREYNRNKEIGLKCNAWKNNCLIDDGNGKVKEMIEATEPKH >ORX84766.1 [Anaeromyces robustus] (SEQ ID No: 81) MVVEKETNKENIKNIKEELDKKHAWVKEMRKKFCVRKEFENTKILILEDGTLNQDYFRLSKGTV LKTNEVRKWTSIERGLLIKGIEKYGIGHFREISENLLPKWSGNDLRIKTIHLIGRQNLKLYKDWK GNEEDIKREYNRNKEIGLKCNAWKNNCLVDDGHGKVKAMIEATENN >ORY98423.1 [Syncephalastrum racemosum] (SEQ ID No: 82) MMTATDEDVDMKDVDIKLESNQETEQKILTPEEQKEKEKQDWIRQLRLKFCIRPEYEITKNMIF PDGTLNQDYFRPPKGAKVEEARKWTEVEKELLIQGIEKYGIGNFGEVSKALLPAWSTNDLRIK CIRLIGRQNLQLYRGWKGNADDIAREYNRNKELGLKYGTWKQGVLVYDDDGLVEKEILAQDA AAKGEDVDMN >XP_021886199.1 [Lobosporangium transversale] (SEQ ID No: 83) MEINQEQLPSSSSILHPTSTSSSSSPSPSPSPASPKPERVFDARQRRINEIRLKFCIRDEFPITK NMIHPDGTLNQDYFRPPRGSKPVEVARKWTDKERELLIKGIEKYGIGHFREISEEFLPLWSGN DLRIKTMRLVGRQNLQLYKDWKGNEQDLAREFELNKAIGLKYGAWKAGTLVADDDGLVAKAI EEQWPGSNSGTGKTTAVIGISSEENSEVSTPLNDEDVDME >ORY01319.1 [Basidiobolus meristosporus CBS 931.73] (SEQ ID No: 84) MEVDQNDSSVAKETAEQPETPEISKELLERQEWIKNMRLQFCVRPEFEVTKNIIHEDGMLNQE YFLPPKGAKLEAEPERKWTETERNLLIQGIQQYGIGHFREISEALLPQWSGNDLRVKSMRLMG RQNLQLYKDWKGSIEDIEREYERNKAIGLKYNTWKNSTLVYDDAGLVLKAIEASEPKP >ORZ26026.1 [Absidia repens] (SEQ ID No: 85) MAIDSLQDTEDDRTNDQNDESRESSPTPLSPEEQAQKERHEDWINQIRLKFCIRPEFEVTKNIIH PDGRLNQEYFHPPKGYKPEDARKWTETEKQLLIKGIEEHGIGNFGLISKESLPKWSTNDLRVK CIRLIGRQNLQLYRGWKGNADDITREYERNKEIGLKYGTWKQGVLVYDDDGMVEKELLATAAT PADSMSMEEDEDMATD >ORX67568.1 [Linderina pennispora] (SEQ ID No: 86) MDTASPDDGAIAQPMLGVEDADFWRQKQEWVKQMRLQFSRRPEFPETHNMIDDEGMLNQE YFQPPKDAVAPKERKWGDDEKRRLLEGIEKHGIGHFREISEESLPEWSGNDLRMKAIRLMGR QNLQLYKGWKGDAAAIGLKHGTWKGGALVYDDDGVVLKAIQESNRANPP >XP_001699352.1 [Chlamydomonas reinhardtii] (SEQ ID No: 87) MAACSAACDSHVVPQPSPGSWGMPEDRDNYIVQMRRRYSPAGMLNADGSINQDFFKPRRV VLVADRAKWGDAEREGLYKGLEVHGVGKWREINRDYLKGQWDDQQVRIRAARLLGSQSLVR YMGWKGSKAKVDAEYAKNKAIGEATGCWKAGQLVEDDHGSVRKYFEAQQAGGEQ Protein sequences for phylogenetic analysis of p2 proteins >XP_001017830.3 [Tetrahymena thermophila SB210] (SEQ ID No: 88) MNQMGVIAIKRKQSYQLNVKINYINTAHQIKKPCQYIQKCILFRLLYKFCKQLIPLNFNLFLIFYFY HLLFHLIFNYLLKFAKKINKLIRNQRKNREKKEAFKHKKIQININHYNYLKQNIQQVGIIFQNKKSK LTLKLVQKKSLSEYYRKIKMKKNGKSQNQPLDFTQYAKNMRKDLSNQDICLEDGALNHSYFLT KKGQYWTPLNQKALQRGIELFGVGNWKEINYDEFSGKANIVELELRTCMILGINDITEYYGKKIS EEEQEEIKKSNIAKGKKENKLKDNIYQKLQQMQ >XP_001699352.1 [Chlamydomonas reinhardtii] (SEQ ID No: 89) MAACSAACDSHVVPQPSPGSWGMPEDRDNYIVQMRRRYSPAGMLNADGSINQDFFKPRRV VLVADRAKWGDAEREGLYKGLEVHGVGKWREINRDYLKGQWDDQQVRIRAARLLGSQSLVR YMGWKGSKAKVDAEYAKNKAIGEATGCWKAGQLVEDDHGSVRKYFEAQQAGGEQ >EJY77156.1 [Oxytricha trifallax] (SEQ ID No: 90) MSTAKQQQAQQHLLPKHSNMRVGSVSNELDYAKRNYIIKMRQSFIEVNKNIYFEDGSLNFKYF NVKKGHYWSKEINEELIKGVIKYGATNYKDIKNKMEIFKKEWSETEIRLRICRLLKCYNLKVYEG HKFNSREEILEQATLNKEEAIKQKKICGGILYNPPHEQDDGIMSSYFNLKNKNNTPVKASAQ >ORZ26026.1 [Absidia repens] (SEQ ID No: 91) MAIDSLQDTEDDRTNDQNDESRESSPTPLSPEEQAQKERHDWINQIRLKFCIRPEFEVTKNIIH PDGRLNQEYFHPPKGYKPEDARKWTETEKQLLIKGIEEHGIGNFGLISKESLPKWSTNDLRVK CIRLIGRQNLQLYRGWKGNADDITREYERNKEIGLKYGTWKQGVLVYDDDGMVEKELLATAAT PADSMSMEEDEDMATD >ORY96423.1 [Syncephalastrum racemosum] (SEQ ID No: 92) MMTATDEDVDMKDVDIKLESNQETEQKILTPEEQKEKEKQDWIRQLRLKFCIRPEYEITKNMIF PDGTLNQDYFRPPKGAKVEEARKWTEVEKELLIQGIEKYGIGNFGEVSKALLPAWSTNDLRIK CIRLIGRQNLQLYRGWKGNADDIAREYNRNKELGLKYGTWKQGVLVYDDDGLVEKEILAQDA AAKGEDVDMN >XP_021886199.1 [Lobosporangium transversale] (SEQ ID No: 93) MEINQEQLPSSSSILHPTSTSSSSSPSPSPSPASPKPERVFDARQRRINEIRLKFCIRDEFPITK NMIHPDGTLNQDYFRPPRGSKPVEVARKWTDKERELLIKGIEKYGIGHFREISEEFLPLWSGN DLRIKTMRLVGRQNLQLYKDWKGNEQDLAREFELNKAIGLKYGAWKAGTLVADDDGLVAKAI EEQWPGSNSGTGKTTAVIGISSEENSEVSTPLNDEDVDME >ORY01319.1 [Basidiobolus meristosporus CBS 931.73] (SEQ ID No: 94) MEVDQNDSSVAKETAEQPETPEISKELLERQEWIKNMRLQFCVRPEFEVTKNIIHEDGMLNQE YFLPPKGAKLEAEPERKWTETERNLLIQGIQQYGIGHFREISEALLPQWSGNDLRVKSMRLMG RQNLQLYKDWKGSIEDIEREYERNKAIGLKYNTWKNSTLVYDDAQLVLKAIEASEPKP >ORX67568.1 [Linderina pennispora] (SEQ ID No: 95) MDTASPDDGAIAQPMLGVEDADFWRQKQEWVKQMRLQFSRRPEFPETHNMIDDEGMLNQE YFQPPKDAVAPKERKWGDDEKRRLLEGIEKHGIGHFREISEESLPEWSGNDLRMKAIRLMGR QNLQLYKGWKGDAAAIGLKHGTWKGGALVYDDDGVVLKAIQESNRANPP >ORX84766.1 [Anaeromyces robustus] (SEQ ID No: 96) MVVEKETNKENIKNIKEELDKKHAWVKEMRKKFCVRKEFENTKILILEDGTLNQDYFRLSKGTV LKTNEVRKWTSIERGLLIKGIEKYGIGHFREISENLLPKWSGNDLRIKTIHLIGRQNLKLYKDWK GNEEDIKREYNRNKEIGLKCNAWKNNCLVDDGHGKVKAMIEATENN >ORX54764.1 [Piromyces finnis] (SEQ ID No: 97) MVVEKDLAQENKIKEELNKKHEWVKEMRKKFCVRKEFENTKNLILEDGTLNQEYFRLSKGTVL KTNEVRKWTSIERNLLIKGIEKYGIGHFREISESLLPKWSGNDLRIKTIHLIGRQNLKLYKDWKG GEEDIKREYNRNKEIGLKCNAWKNNCLIDDGNGKVKEMIEATEPKH >ORX56334.1 [Hesseltinella vesiculosa] (SEQ ID No: 98) MLAGDAELVEKPHNALNAEDTEMEDVDHSSHPDTTVDLSPEQLRLQEKQAWINQMRLKFCV REEFEITKNMIHPDGILNQDYFKPPKKSKKKKSKSKSKGTDETKDDTEAKGEDNKEDEDME >PNW76495.1 [Chlamydomonas reinhardtii] (SEQ ID No: 99) MAFAAALAEKRGPRVGDAASLWNFTPAPGWSREEVQILRLCLMKHGVGQWMQILSTGLLPG KLIQQLNGQTQRLLGQQSLAAYTGLKVDVDRIRVDNETRTDATRKAGLIINDGPNLTKEMKEK MRQDAVAKYGLTPEQVAEVDEQLAEIAAAFNPASTSAAAGAGSGAAAAGQAAAAGSGAGGS GQAATAADAGGAAGRGTGSAGGAAAAAPPRNALAISTGVLAATLLDASLGNLMAQPTEQLSA EQLGQLLLRLRNRLACLVDRARGRAGLPPRTAPRWATEAAAAACLAAMAAAEASAPQAPAAA AGGQEGAAGPVMVSVPFSREVLAEATACRVRSGTAAGARGNAPGAQGGVRKRTSKGGKAK GGDREWSPEGEENTAPQPRGGGKRKSGAVAGGEEADGVASGRAKRASRPKRGSSKHDPY VDDNDYGDEGIDPFDVGDDLDDMNPHGRYGNGGGRRADPSEAISALTAMGFTQSKARGALR ECNFNVELAVEWLFANCL >XP_001698763.1 [Chlamydomonas reinhardtii] (SEQ ID No: 100) MAFAAALAEKRGPRVGDAASLWNFTPAPGWSREEVQILRLCLMKHGVGQWMQILSTGLLPG KLIQQLNGQTQRLLGQQSLAAYTGLKVDVDRIRVDNETRTDATRKAGLIINDGPNLTKEMKEK MRQDAVAKYGLTPEQVAEVDEQLAEIAAAFNPASTSAAAGAGSGAAAAGQAAAAGSGAGGS GNLMAQPTEQLSAEQLGQLLLRLRNRLACLVDRARGRAGLPPRTAPRWATEAAAAACLAAM AAAEASAPQAPAAAAGGQEGAAGPVMVSVPFSREVLAEATACRVRSGTAAGARGNAPGAQ GGVRKRTSKGGKAKGGDREWSPEGEENTAPQPRGGGKRKSGAVAGGEEADGVASGRAKR ASRPKRGSSKHDPYVDDNDYGDEGIDPFDVGDDLDDMNPHGRYGNGGGRRADPSEAISALT AMGFTQSKARGALRECNFNVELAVEWLFANCL >XP_011237366.1 [Mus musculus] (SEQ ID No: 101) MPRRQAEAMDIDAEREKITQEIQELERILYPGSTSVHFEVSESSLSSDSEADSLPDEDLETAGA PILEEEGSSESSNDEEDPKDKALPEDPETCLQLNMVYQEVIREKLAEVSQLLAQNQEQQEEILF DLSGTKCPKVKDGRSLPSYMYIGHFLKPYFKDKVTGVGPPANEETREKATQGIKAFEQLLVTK WKHWEKALLRKSVVSDRLQRLLQPKLLKLEYLHEKQSRVSSELERQALEKQIKEAEKEIQDIN QLPEEALLGNRLDSHDWEKISNINFEGARSAEEIRKFWQSSEHPSISKQEWSTEEVERLKAIA ATHGHLEWHLVAEELGTSRSAFQCLQKFQQYNKTLKRKEWTEEEDHMLTQLVQEMRVGNHI PYRKIVYFMEGRDSMQLIYRWTKSLDPSLKRGFWAPEEDAKLLQAVAKYGAQDWFKIREEVP GRSDAQCRDRYIRRLHFSLKKGRWNAKEEQQLIQLIEKYGVGHWARIASELPHRSGSQCLSK WKILARKKQHLQRKRGQRPRHSSQWSSSGSSSSSSEDYGSSSGSDGSSGSENSDVELEAS LEKSRALTPQQYRVPDIDLWVPTRLITSQSQREGTGCYPQHPAVSCCTQDASQNHHKEGSTT VSAAEKNQLQVPYETHSTVPRGDRFLHFSDTHSASLKDPACKPVLKVPLEKMPKLIRTRPPTQ SHTLMKERPKQPLLPSSRSGSDPGNNTAGPHLRQLWHGTYQNKQRRKRQALHRRLLKHRLL LAVIPWVGDINLACTQAPRRPATVQTKADSIRMQLECARLASTPVFTLLIQLLQIDTAGMEVV RERKSQPPALLQPGTRNTQPHLLQASSNAKNNTGCLPSMTGEQTAKRASHKGRPRLGSCRT EATPFQVPVAAPRGLRPKPKTVSELLREKRLRESHAKKATQALGLNSQLLVSSPVILQPPLLPV PHGSPVVGPATSSVELSVPVAPVMVSSSPSGSWPVGGISATDKQPPNLQTISLNPPHKGTQV AAPAAFRSLALAPGQVPTGGHLSTLGQTSTTSQKQSLPKVLPILRAAPSLTQLSVQPPVSGQP LATKSSLPVNWVLTTQKLLSVQVPAVVGLPQSVMTPETIGLQAKQLPSPAKTPAFLEQPPAST DTEPKGPQGQEIPPTPGPEKAALDLSLLSQESEAAIVTWLKGCQGAFVPPLGSRMPYHPPSL CSLRALSSLLLQKQDLEQKASSLAASQAAGAQPDPKAGALQASLELVQRQFRDNPAYLLLKTR FLAIFSLPAFLATLPPNSIPTTLSPDVAVVSESDSEDLGDLELKDRARQLDCMACRVQASPAAP DPVQSHLVSPGQRAPSPGEVSAPSPLDASDGLDDLNVLRTRRARHSRR >XP_006497966.1 [Mus musculus] (SEQ ID No: 102) MPRRQAEAMDIDAEREKITQEIQELERILYPGSTSVHFEVSESSLSSDSEADSLPDEDLETAGA PILEEEGSSESSNDEEDPKDKALPEDPETCLQLNMVYQEVIREKLAEVSQLLAQNQEQQEEILF DLSGTKCPKVKDGRSLPSYMYIGHFLKPYFKDKVTGVGPPANEETREKATQGIKAFEQLLVTK WKHWEKALLRKSVVSDRLQRLLQPKLLKLEYLHEKQSRVSSELERQALEKQIKEAEKEIQDIN QLPEEALLGNRLDSHDWEKISNINFEGARSAEEIRKFWQSSEHPSISKQEWSTEEVERLKAIA ATHGHLEWHLVAEELGTSRSAFQCLQKFQQYNKTLKRKEWTEEEDHMLTQLVQEMRVGNHI PYRKIVYFMEGRDSMQLIYRWTKSLDPSLKRGFWAPEEDAKLLQAVAKYGAQDWFKIREEVP GRSDAQCRDRYIRRLHFSLKKGRWNAKEEQQLIQLIEKYGVGHWARIASELPHRSGSQCLSK WKILARKKQHLQRKRGQRPRHSSQWSSSGSSSSSSEDYGSSSGSDGSSGSENSDVELEAS LEKSRALTPQQYRVPDIDLWVPTRLITSQSQREGTGCYPQHPAVSCCTQDASQNHHKEGSTT VSAAEKNQLQVPYETHSTVPRGDRFLHFSDTHSASLKDPACKSHTLMKERPKQPLLPSSRSG SDPGNNTAGPHLRQLWHGTYQNKQRRKRQALHRRLLKHRLLLAVIPWVGDINLACTQAPRRP ATVQTKADSIRMQLECARLASTPVFTLLIQLLQIDTAGCMEVVRERKSQPPALLQPGTRNTQP HLLQASSNAKNNTGCLPSMTGEQTAKRASHKGRPRLGSCRTEATPFQVPVAAPRGLRPKPK TVSELLREKRLRESHAKKATQALGLNSQLLVSSPVILQPPLLPVPHGSPVVGPATSSVELSVPV APVMVSSSPSGSWPVGGISATDKQPPNLQTISLNPPHKGTQVAAPAAFRSLALAPGQVPTGG HLSTLGQTSTTSQKQSLPKVLPILRAAPSLTQLSVQPPVSGQPLATKSSLPVNWVLTTQKLLSV QVPAVVGLPQSVMTPETIGLQAKQLPSPAKTPAFLEQPPASTDTEPKGPQGQEIPPTPGPEKA ALDLSLLSQESEAAIVTWLKGCQGAFVPPLGSRMPYHPPSLCSLRALSSLLLQKQDLEQKASS LAASQAAGAQPDPKAGALQASLELVQRQFRDNPAYLLLKTRFLAIFSLPAFLATLPPNSIPTTLS PDVAVVSESDSEDLGDLELKDRARQLDCMACRVQASPAAPDPVQSHLVSPGQRAPSPGEVS APSPLDASDGLDDLNVLRTRRARHSRR >EJY86254.1 [Oxytricha trifallax] (SEQ ID No: 103) MSVHHKMADSKSLHNYTLSPGWTREEVDILKIALMKFGIGKWKKIQKSGCLPSKTISQMNLQT QRLLGQQSLAEFMGLHVYLDRVFRDNSLKTGPEIQRKNNFIINTGNNLTQPEKEKRLRLNKQK YGLDLAFIKTLRLPKPESATGGKREAILSMDQIFAQKSHFTVVEKLKHLEALKNALCSKLGKIER RRRNKELSKIYRPLCQLIVVQKNADDQYEFVDIIDENE >ORX69504.1 [Linderina pennispora] (SEQ ID No: 104) MSSATPYAPRSMPTGQRNVVRSNDSASLWNCTLSPGWTQEEVQVLRKALMKFGVGNWMKII ESECLPGKTIAQMNLQTQRMLGQQSTAEFNGLHLDAFVIGELNSKKQGPGIKRKNNCIVNTGG KLTRDEVVKRQQKHREQYEVKAEVWRAIVLPKPDNPLILLEKKREELKKVRLELEEIMKQIEET EKLVDVPEHAPGTKRARE >NP_003077.2 [Homo sapiens] (SEQ ID No: 105) MDVDAEREKITQEIKELERILDPGSSGSHVEISESSLESDSEADSLPSEDLDPADPPISEEERW GEASNDEDDPKDKTLPEDPETCLQLNMVYQEVIQEKLAEANLLLAQNREQQEELMRDLAGSK GTKVKDGKSLPPSTYMGHFMKPYFKDKVTGVGPPANEDTREKAAQGIKAFEELLVTKWKNW EKALLRKSVVSDRLQRLLQPKLLKLEYLHQKQSKVSSELERQALEKQGREAEKEIQDINQLPEE ALLGNRLDSHDWEKISNINFEGSRSAEEIRKFWQNSEHPSINKQEWSREEEERLQAIAAAHGH LEWQKIAEELGTSRSAFQCLQKFQQHNKALKRKEWTEEEDRMLTQLVQEMRVGSHIPYRRIV YYMEGRDSMQLIYRWTKSLDPGLKKGYWAPEEDAKLLQAVAKYGEQDWFKIREEVPGRSDA QCRDRYLRRLHFSLKKGRWNLKEEEQLIELIEKYGVGHWAKIASELPHRSGSQCLSKWKIMM GKKQGLRRRRRRARHSVRWSSTSSSGSSSGSSGGSSSSSSSSSEEDEPEQAQAGEGDRAL LSPQYMVPDMDLWVPARQSTSQPWRGGAGAWLGGPAASLSPPKGSSASQGGSKEASTTA AAPGEETSPVQVPARAHGPVPRSAQASHSADTRPAGAEKQALEGGRRLLTVPVETVLRVLRA NTAARSCTQKEQLRQPPLPTSSPGVSSGDSVARSHVQWLRHRATQSGQRRWRHALHRRLL NRRLLLAVTPWVGDVVVPCTQASQRPAVVQTQADGLREQLQQARLASTPVFTLFTQLFHIDT AGCLEVVRERKALPPRLPQAGARDPPVHLLQASSSAQSTPGHLFPNVPAQEASKSASHKGSR RLASSRVERTLPQASLLASTGPRPKPKTVSELLQEKRLQEARAREATRGPVVLPSQLLVSSSVI LQPPLPHTPHGRPAPGPTVLNVPLSGPGAPAAAKPGTSGSWQEAGTSAKDKRLSTMQALPL APVFSEAEGTAPAASQAPALGPGQISVSCPESGLGQSQAPAASRKQGLPEAPPFLPAAPSPT PLPVQPLSLTHIGGPHVATSVPLPVTWVLTAQGLLPVPVPAVVSLPRPAGTPGPAGLLATLLPP LTETRAAQGPRAPALSSSWQPPANMNREPEPSCRTDTPAPPTHALSQSPAEADGSVAFVPG EAQVAREIPEPRTSSHADPPEAEPPWSGRLPAFGGVIPATEPRGTPGSPSGTQEPRGPLGLE KLPLRQPGPEKGALDLEKPPLPQPGPEKGALDLGLLSQEGEAATQQWLGGQRGVRVPLLGS RLPYQPPALCSLRALSGLLLHKKALEHKATSLVVGGEAERPAGALQASLGLVRGQLQDNPAYL LLRARFLAAFTLPALLATLAPQGVRTTLSVPSRVGSESEDEDLLSELELADRDGQPGCTTATC PIQGAPDSGKCSASSCLDTSNDPDDLDVLRTRHARHTRKRRRLV >XP_016870547.1 [Homo sapiens] (SEQ ID No: 106) MDVDAEREKITQEIKELERILDPGSSGSHVEISESSLESDSEADSLPSEDLDPADPPISEEERW GEASNDEDDPKDKTLPEDPETCLQLNMVYQEVIQEKLAEANLLLAQNREQQEELMRDLAGSK GTKVKDGKSLPPSTYMGHFMKPYFKDKVTGVGPPANEDTREKAAQGIKAFEELLVTKWKNW EKALLRKSVVSDRLQRLLQPKLLKLEYLHQKQSKVSSELERQALEKQGREAEKEIQDINQLPEE ALLGNRLDSHDWEKISNINFEGSRSAEEIRKFWQNSEHPSINKQEWSREEEERLQAIAAAHGH LEWQKIAEELGTSRSAFQCLQKFQQHNKALKRKEWTEEEDRMLTQLVQEMRVGSHIPYRRIV YYMEGRDSMQLIYRWTKSLDPGLKKGYWAPEEDAKLLQAVAKYGEQDWFKIREEVPGRSDA QCRDRYLRRLHFSLKKGRWNLKEEEQLIELIEKYGVGHWAKIASELPHRSGSQCLSKWKIMM GKKQGLRRRRRRARHSVRWSSTSSSGSSSGSSGGSSSSSSSSSEEDEPEQAQAGEGDRAL LSPQYMVPDMDLWVPARQSTSQPWRGGAGAWLGGPAASLSPPKGSSASQGGSKEASTTA AAPGEETSPVQVPARAHGPVPRSAQASHSADTRPAGAEKQALEGGRRLLTVPVETVLRVLRA NTAARSCTQWLRHRATQSGQRRWRHALHRRLLNRRLLLAVTPWVGDVVVPCTQASQRPAV VQTQADGLREQLQQARLASTPVFTLFTQLFHIDTAGCLEVVRERKALPPRLPQAGARDPPVHL LQASSSAQSTPGHLFPNVPAQEASKSASHKGSRRLASSRVERTLPQASLLASTGPRPKPKTV SELLQEKRLQEARAREATRGPVVLPSQLLVSSSVILQPPLPHTPHGRPAPGPTVLNVPLSGPG APAAAKPGTSGSWQEAGTSAKDKRLSTMQALPLAPVFSEAEGTAPAASQAPALGPGQISVSC PESGLGQSQAPAASRKQGLPEAPPFLPAAPSPTPLPVQPLSLTHIGGPHVATSVPLPVTWVLT AQGLLPVPVPAVVSLPRPAGTPGPAGLLATLLPPLTETRAAQGPRAPALSSSWQPPANMNRE PEPSCRTDTPAPPTHALSQSPAEADGSVAFVPGEAQVAREIPEPRTSSHADPPEAEPPWSGR LPAFGGVIPATEPRGTPGSPSGTQEPRGPLGLEKLPLRQPGPEKGALDLEKPPLPQPGPEKG ALDLGLLSQEGEAATQQWLGGQRGVRVPLLGSRLPYQPPALCSLRALSGLLLHKKALEHKAT SLVVGGEAERPAGALQASLGLVRGQLQDNPAYLLLRARFLAAFTLPALLATLAPQGVRTTLSV PSRVGSESEDEDLLSELELADRDGQPGCTTATCPIQGAPDSGKCSASSCLDTSNDPDDLDVL RTRHARHTRKRRRLV >XP_020936800.1 [Sus scrofa] (SEQ ID No: 107) MDVDAEREKISKEIKELERILDPGSSGINDDVSESSLDSDSEAESLPDDDADATGPLLSEDERW GDASNDEDDAKERALPEDPETCLQLNMVYQEVVREKLAEVSLLLAQNREQQEEVSWALAGS GGRRVKDGRSPPARLYVGHFMKPYFKDKVTGAGPPANEDTREKAAQGVKAFEELLVTKWKS WEKALLRKAVVSDRLQRLLQPKLLKLEYLQQKQSRATSDAERQALEKQVREAEKEVQDISQL PEEALLGHRLDSHDWEKIANVNFEGGRSAEETRKFWQNHEHPSINKQEWSAQEVDRLKAIAA KHGHLRWQEIAEELGTRRSAFQCLQKYQQHNAALKRREWTQEEDRMLTQLVQAMGVGSHIP YRRIAYYMEGRDSTQLIYRWTKSLDPALKKGLWAPEEDAKLLQAVAKYGEQDWFKIREEVPG RSDAQCRDRYLRRLRLSLKKGRWSAQEEERLLELIGKHGVGHWAKIASELPHRTDSQCLSK WKIMARKQQSRGRRRRRPLRRVCWSSSSEDSEDSGDSGGSSSSSSSSEDVEPEGAPEARA DGPAPPSAQHPVPDMDLWVPTRQSARVPWGVGPGAWPGHRSASPRPPEGSDVAPGEEAG RAQAPSETPSASLRGGGCPRSADARPSGSEGLADEGPRRPLTVPLETVLRVLRTNTAALCRA LKEKLRRPRLLGSPLGPSPSDGSVARPRVQPRWRRRHALQRRLLERQLLMAVSPWVGDVTL PCAPWRPAVLHRRADGIGKQLQGARLASTPVFTLLIQLFRIDTAGCMEVVRERRAQPPALPSG GRVPSSARNSPGHLFQNGSARGAAKKSASHSGGGGPQSAPAPSGPRPKPKTVSELLREKRL REARARKAAQGPAVLPPQGLLSSPAILQPLPPQQLPVSGAVLSGPGGPAVASPGAPGPWAS AKEGPPSLHALALAPASMAAGVTPAAPRAPALGPSQVPASCHLSSLGQSQAPATSRKQGLPE APPFLPAAPSPIQLPVQPRSLTPALAAHTGASHVVASTPLPVTWVLTAQGLLPVPAVVGLPRP AGPPDPEGLSGTPPPSLTETRAGRGPKQPPAHVSVGPDPPAKTPPTAQSPAEGDGDVAHGP GGPSCPGEAQVAGEASVPRTLSPAKPLADHPEAEPCGSSQLPLPGGLSPGGAPTRHQGLER PPPPWPGPEKGAPDLRLLSQESEAAVRGWLTGQRGVCVPPLASRLPYQPPTLCSLRALSGLL LHKKALEHRAASLVPSGAAGAQQAPLGQVRERLQSSPAYLLLKARFLAAFALPALLATLPPHG VPTTLSAAAGVDSESDDDSLDELELADNGGPLGGWPSGRQAGPAAPTPTQGAPGEGSAAP GLDSDDLDILRTRHAWHARKRRRLV >XP_021883515.1 [Lobosporangium transversale] (SEQ ID No: 108) MSSGSTPRSMTAGARNILRSNDSASLWNYTVAPGWSMKEAEILRKALMKFGIGNWSKIIESN CLVGKTNAQMNLQTQRMLGQQSTAEFAGLHIDPRVIGQKNSLIQGDHIRRKNGCIVNTGAKLS REEIRRRVAENKEQYELPEEEWSSIELPLPDDPHLLLEAKKSEKVRLELELKNVQRQIAMLRKV GRKFETGSESPKTELDDDERDEFIEDQPLGKRARIEA >EJY76686.1 [Oxytricha trifallax] (SEQ ID No: 109) MRVYLKFCNRKQIHYTHTMSSSISAAIMAGNQNKKIAESKSLWNYALSPGWTQQEVEILKIALM KFGVGRWSAINKSGVLPTKQIQQCYLQTQRLIGQQSLAEFMGLHLDIDRIAADNKQKRGIRKQ GFLVNQGCKLTPEEKDELRKINQEKYGLTAEHVEAIKLPAPCHLVEIFQIDKIMHPRSTLSTMDK IKHLIKLEDALKSKLEMIREGKRQQKFEQLQQKLKTTEASGRGSVTRVQRQMSDLHLGSAHQN RNSDLDEENDQSVMIIDESQQQNLTPKGKAQTMLTNQTQTMKKQADDSRDEQHLPLISTSAS VSNPSSTSKSSALKLNSMKQSDTAIASMKPSSSGKKTKVDSSFVSKQSNQQSTSYSETNVDT QNSNNQGTSTASGNFISQSDDEEALMPKLKRRRVEDSE >EJY73777.1 [Oxytricha trifallax] (SEQ ID No: 110) MSHATSHGNSTEKDKKNSGNMVAESKSLWNYALSPGWTPQEVDVLKIALMKFGIGKWTIIDK SGILPTKTIQQCYLQTQRILGQQSLAEFMGLHVDIDKIALDNRRKNGIRKMGFLVNQGGKLTPE EKAHYQEINRQKYGLSPEEVETIKLPPPCSVEIYDINKIINPKSKLTTIEKINHCIKLQDALLEKLEN IKNKKIPTGAGFSSSRVYENMRGYDPQLLLNSHVTGQLDHSMQDLTIDERYSDLDEEEDPLAM ASIIDSQATPQPQKIKSSVPNKASTTPSAKEMNQIKDIIDSVIAENSAQQSKNLAQEKPKLKFSLV KATESNLLQSAAQNSDDVVMEEDSKLQHIETFSTVTQTATDQSNSQSKSQNNIASDSLKDSLE QNDLSKSLTDSLEMQQYSAEKKLNQAPMSKNSDKPKKKRLNKRKLPSDDEFETL >EJY79729.1 [Oxytricha trifallax] (SEQ ID No: 111) MSSSISAAIIAGNQNKKIAESKSLWNYALSPGWTQQEVEILKIALMKFGVGRWKTIEQSQCLPT KTMSQMYLQTQRLVGQQSLAEFMGLHLDLEQIFIKNAERQGAGVFRKNGCIINTGDNMTKVQI AKLRKKNSKIFGLTQPFVQSLHLPKAKVKEWLKVLTLDQILSAKSNFSTAEKIHYLKILENALER KLKKILRLQELVSIYRPCNIGIVVQKRLGSSIGDEYFEYVDCVKIEEKSVGNLDFALPNRNTDSTS LNEDFSFLDSTQKPQKLKAGSGRENKRKKMRDGLKDERAQRQSLMEALDEQEFDETKFQDS DGEMPDLNM >EJY81929.1 [Oxytricha trifallax] (SEQ ID No: 112) MSSSISAAIMAGNQNKKIAESKSLWNYALSPGWTQQEVEILKIALMKFGVGRWSAINKSGVLP TKQIQQCYLQTQRLIGQQSLAEFMGLHLDIDRIAADNKQKRGIRKQGFLVNQGCKLTPEEKDEL RKINQEKYGLSAEHVEAIKLPAPCHLVEIFQIDKIMHPRSTLSTMDKIKHLIKLEDALKSKLEMIRE GKRQQKFEQLQQKLKTTEASGRGSVTRVQRQMSDLHLGSSHQNRNSDLDEENDESVMIIDE SQQENLTPKGKAQAMLTHQKYNEVTQTMIKQGDDSRQQQHLPLDSTSASVSNPSSTSKSST MKSNSMKQSETAIASMKPSSIGKKTKVDSSFVTKQSNQQSTAPIQKQAHQQNLDRNRSELGS TFAQQASVDTQNSNNQGTSTASGNFISQSDDEEALMPKLKRRRVEDSE >EJY80746.1 [Oxytricha trifallax] (SEQ ID No: 113) MRVYLKFCNRKQIHYTHTMSSSISAAIMAGNQNKKIAESKSLWNYALSPGWTQQEVEILKIALM KFGVGRWSAINKSGVLPTKQIQQCYLQTQRLIGQQSLAEFMGLHLDIDRIAADNKQKRGIRKQ GFLVNQGCKLTPEEKDELRKINQEKYGLTAEHVEAIKLPAPCHLVEIFQIDKIMHPRSTLSTMDK IKHLIKLEDALKSKLEMIREGKRQQKFEQLQQKLKTTEASGRGSVTRVQRQMSDLHLGSAHQN RNSDLDEENDQSVMIIDESQQQNLTPKGKAQTMLTNQTQTMKKQADDSREEQHLPLNSTSAS VSNPSSTSKSSALKLNSMKQSDTAIASMKPSSSGKKTKVDSSFVSKQSNQQSTGPIQKQAHQ QNLDRNRSELGSTFAQQTNVDTQNSNNQGTSTASGNFISQSDDEEALMPKLKRRRVKDSE >ORX78557.1 [Basidiobolus meristosporus CBS 931.73] (SEQ ID No: 114) MTDVYKPRSMPVGARNVLRSNDSASLWNCTLSPGWTEPEVHILRKAVMKFGIGNWAKIIESQ CLFGKTIAQMNLQLQRMLGQQSTAEFAGLHLDPFVIGEINSKKQGPGIKRKNNCIVNTGGKLTR EEIKRRLLEHKRTYEISEEEWRSIELPKPEDPGAVLIAKKDELKMLEDELLRVVQKIQKAREERR SKSVDSSSVDGSVDDEARETKRRRK >ORX79686.1 [Anaeromyces robustus] (SEQ ID No: 115) MSIPKPRSMPTGFRNILRPNDSTSLWNCTLSPGWTQEESDILRDALIYYGIGNWKDIIEHGCLP DKTNAQMNLQLQRMLGQQSTAEFQNLHIDPYVIGKINSQKQGPNIRRKNGFIINTGGKLSREDI RRKIQENKENYELPKEEWSKIVLPNREVVIKNKVQEAINEKREKLNKLEDELDSVLKAIVNRRR ELRGMIPLKDSEMKSLVNRSAKNEGENKTETTNNEESNNTNNSDDIKDENNETSTSSHIFTNN DNELSENNSSSSSSNSISNKKKRFLRREVRRGKRRYNYDDDDFMPSGNRSRKSRKI >ORX56566.1 [Piromyces finnis] (SEQ ID No: 116) MSIPKPRSMPVGFRNILRPNDSTSLWNCTLSPGWTQEESDILRDALIFYGIGNWKDIIEHGCLP DKTNAQMNLQLQRMLGQQSTAEFQNLHIDPYEIGKINSQKQGPNIRRKNGFIINTGGKLSREDI KRKIQENKENYELPEEVWSKIVLPNREVVTINEKRQKLNKLEEELDSVLKQIVNRRRELRGMTP LKETEMKSIVNRSNQNDTKTEEKEIKEEESTTVNEEKIENTETSSISIISTNENEQSENISSSSPIV KSEQKKKRVVSRRKNKRRVNSDDEDFLPPGKSRSKRTRRTPKKSSN >XP_001009903.1 [Tetrahymena thermophila SB210] (SEQ ID No: 117) MSLKKGKFQHNQSKSLWNYTLSPGWREEEVKILKSALQLFGIGKWKKIMESGCLPGKSIGQIY MQTQRLLGQQSLGDFMGLQIDLEAVFNQNMKKQDVLRKNNCIINTGDNPTKEERKRRIEQNR KIYGLSAKQIAEIKLPKVKKHAPQYMTLEDIENEKFTNLEILTHLYNLKAEIVRRLAEQGETIAQPS IIKSLNNLNHNLEQNQNSNSSTETKVTLEQSGKKKYKVLAIEETELQNGPIATNSQKKSINGKRK NNRKINSDSEGNEEDISLEDIDSQESEINSEEIVEDDEEDEQIEEPSKIKKRKKNPEQESEEDDI EEDQEEDELVVNEEEIFEDDDDDEDNQDSSEDDDDDED >XP_020936799.1 [Sus scrofa] (SEQ ID No: 118) MDVDAEREKISKEIKELERILDPGSSGINDDVSESSLDSDSEAESLPDDDADATGPLLSEDERW GDASNDEDDAKERALPEDPETCLQLNMVYQEVVREKLAEVSLLLAQNREQQEEVSWALAGS GGRRVKDGRSPPARLYVGHFMKPYFKDKVTGAGPPANEDTREKAAQGVKAFEELLVTKWKS WEKALLRKAVVSDRLQRLLQPKLLKLEYLQQKQSRATSDAERQALEKQVREAEKEVQDISQL PEEALLGHRLDSHDWEKIANVNFEGGRSAEETRKFWQNHEHPSINKQEWSAQEVDRLKAIAA KHGHLRWQEIAEELGTRRSAFQCLQKYQQHNAALKRREWTQEEDRMLTQLVQAMGVGSHIP YRRIAYYMEGRDSTQLIYRWTKSLDPALKKGLWAPEEDAKLLQAVAKYGEQDWFKIREEVPG VTFEARAFPASRQRTSLPCAPLWPPALWVSRLGNRRGGRQPRGFSRTPRSVCRRYLRRLRL SLKKGRWSAQEEERLLELIGKHGVGHWAKIASELPHRTDSQCLSKWKIMARKQQSRGRRRR RPLRRVCWSSSSEDSEDSGDSGGSSSSSSSSEDVEPEGAPEARADGPAPPSAQHPVPDMD LWVPTRQSARVPWGVGPGAWPGHRSASPRPPEGSDVAPGEEAGRAQAPSETPSASLRGG GCPRSADARPSGSEGLADEGPRRPLTVPLETVLRVLRTNTAALCRALKEKLRRPRLLGSPLGP SPSDGSVARPRVQPRWRRRHALQRRLLERQLLMAVSPWVGDVTLPCAPWRPAVLHRRADG IGKQLQGARLASTPVFTLLIQLFRIDTAGCMEVVRERRAQPPALPSGGRVPSSARNSPGHLFQ NGSARGAAKKSASHSGGGGPQSAPAPSGPRPKPKTVSELLREKRLREARARKAAQGPAVLP PQGLLSSPAILQPLPPQQLPVSGAVLSGPGGPAVASPGAPGPWASAKEGPPSLHALALAPAS MAAGVTPAAPRAPALGPSQVPASCHLSSLGQSQAPATSRKQGLPEAPPFLPAAPSPIQLPVQ PRSLTPALAAHTGASHVVASTPLPVTWVLTAQGLLPVPAVVGLPRPAGPPDPEGLSGTPPPSL TETRAGRGPKQPPAHVSVGPDPPAKTPPTAQSPAEGDGDVAHGPGGPSCPGEAQVAGEAS VPRTLSPAKPLADHPEAEPCGSSQLPLPGGLSPGGAPTRHQGLERPPPPWPGPEKGAPDLR LLSQESEAAVRGWLTGQRGVCVPPLASRLPYQPPTLCSLRALSGLLLHKKALEHRAASLVPS GAAGAQQAPLGQVRERLQSSPAYLLLKARFLAAFALPALLATLPPHGVPTTLSAAAGVDSESD DDSLDELELADNGGPLGGWPSGRQAGPAAPTPTQGAPGEGSAAPGLDSDDLDILRTRHAWH ARKRRRLV >XP_009300052.1 [Danio rerio] (SEQ ID No: 119) MKCLSVNMTHLSRDSWLYTHDVQVTYNSFIKVSPCPKMASDDLRAQRDKIQREILALESTLGA DSSIADQLSSDNSSDYESDDSGPTVKRVERDDLETERLRIQREIEELENALGADAALENVLQD SDHDTDSSEDSADDLELPQNVETCLQMNLVYQEVLKEKLAELEQLLIENQQQQKEIEVQLSGP GNSIFSVPGVPPQKQFLGYFLKPYFKDKLTGLGPPANEETKERMKHGSIPVDNLKIKRWEGW QKTLLTNAVARDTMKRMLQPKLSKMEYLSNKLCRAEGEEKEQLKAQIELIEKQIAEIRTLKDDQ LLGDLQDDHDWDKISNIDFEGLRQADDLKRFWQNFLHPSINKSVWKQDEIYKLQAVAEEFKM CHWDKIAEALGTNRTAFMCFQTYQRYISKTFRRTHWTEEEDDLLRELVEKMRIGNFIPYIQMS HFMVGRDGSQLAYRWTSVLDPSLKKGPWSKEEDQLLRNAVAKYGTREWGRIRTEVPGRTD SACRDRYLDCLRETVKKGTWSYAEMELLKEKVAKYGVGKWAKIASEIPNRVDAQCLHKWKL MTRSKKPLKRPLSSITTSYPRNKRQKLLKTVKEEMFFNSSSDDESQINYMNSDESDDLAEDEN LEIPQKEYVQTEMKEWIPRNAMVWTITPGSFRTLWVRLPTNEEELRESTKESGLGSDSSENS ACPNDEPIMERNTILDRFGDVERTYVGMNTVVLHRRTDDEKAMFKVCMSDVKQFIQMKATEF AVKKKKKIKNKKRTLRDVFSLNTDLQKAVIPWIGNVIISTPANEAIFCEGDIVGIKAASIRLQKTSV FTFFIKAFHVDVNGCRTVIEIHKKLDIKMPLAINGNPKPTPISTSPKTVAVLLQQSKAASEHKKPA EPSQQPSLPPSQKPSLPPAQQPTQPPSLPPSVPPSQQPTLPPPSQPSQPPPQPPSLPPSQPP AQQPPQQPSLPPPQPPSLPPPQPPSLPTSQQQSLPPSQQHSLPPFQNPSLPPSQQPSLPPS KQPPQPLPVRQITTPTLIYPNNLVITNPNMEGEVQHLVFKGLLLPQQPSKAVSHIPLPVMQPKT PAQPIVVSKSPSVQDSNSVKSSKRICKPTKKAQALMEQSKVKSRKKEPQKQNQGNKNVVFPT VTLQTSPVIKILSPARLVQVTGLSPNFSSNQTINMPDKSLTIKSPQPCSSGNLHQSAPVVVHSS TNPTFVHSSVSNVSRDNLNVSSTINISPRVSRDALNPTSFLNSTTFPLPQNLSVQQSVQIVPQIP INVVHKATCTKAAKTSSDSSSDESVVKQHQLSPSTGRSIPPAVFNIQPNPSTPPTLSSGPVIFN PNNKVVAPKLCGLNVSSSQLPTVSTQKTKYRPIRPLGPLPVVAPPSRKVTSMSRIRAQSEGEP LISLRDLPAAGVNFDSHLIFPEKSSEVDDWMDGKGGIPLPHLDTSLPYLPPSAATIKTMTDLLRA KQPLLLAAKKVLPAQYQDECNEEVEVEAIRKVVAERFASNPAYLLCKARFLSCFTLPALLATINP CEERQLLSEDDEEDDHLATINPSEEHQSSTEDDEEDLQTNERSQPPTARTELNMNENEASAK QFSGIGPKRQRNQRIKRLIK

TABLE-US-00003 TABLE 2 Primer sequences. Name Sequence (5′ to 3′) Description 1781.0_qF24 ACTAGTCTTAAATATGAGAAAGATGATTTGAA Contig1781.0 tiling qPCR TAAGAT (SEQ ID No: 120) primers 1781.0_qR24 ATCCTAGCAATATTATCTACTTATAATTCTATT Contig1781.0 tiling qPCR GACTATTAG (SEQ ID No: 121) primers 1781.0_qF23 CTAATTAACTAATAGTCAATAGAATTATAAGT Contig1781.0 tiling qPCR AGATAATATTGCT (SEQ ID No: 122) primers 1781.0_qR23 CATTAAATCATTAACAGAGTAATGTCGTCATA Contig1781.0 tiling qPCR TATTTGTC (SEQ ID No: 123) primers 1781.0_qF22 TTTAGTGAGCATAGACAAATATATGACGACAT Contig1781.0 tiling qPCR TACTC (SEQ ID No: 124) primers 1781.0_qR22 GCGGAGATGTCTTTTTGACCTTTTGATAG Contig1781.0 tiling qPCR (SEQ ID No: 125) primers 1781.0_qF21 ATGTTAACATGCTTATTATTACTATCAAAAGG Contig1781.0 tiling qPCR TCAA (SEQ ID No: 126) primers 1781.0_qR21 GGCTGCTACTGATATTTATGTTCTTTATGTTT Contig1781.0 tiling qPCR A (SEQ ID No: 127) primers 1781.0_qF20 CAAAGAACACGAAGCTCATAAACATAAAGAA Contig1781.0 tiling qPCR CAT (SEQ ID No: 128) primers 1781.0_qR20 TGGAGCAAATGCTGCTAATAACGAG (SEQ ID Contig1781.0 tiling qPCR No: 129) primers 1781.0_qF19 ACCTCCAGCAGCTCCGTTTCTATTATTTG Contig1781.0 tiling qPCR (SEQ ID No: 130) primers 1781.0_qR19 GGCCTGGGTATTTTCCCTGCTTTA (SEQ ID Contig1781.0 tiling qPCR No: 131) primers 1781.0_qF18 CTTCCCAGGTAAAATTTAAGGTAAATAAAGCA Contig1781.0 tiling qPCR GG (SEQ ID No: 132) primers 1781.0_qR18 TCAAGGTGGAGGACTCTTCGGTAAC (SEQ ID Contig1781.0 tiling qPCR No: 133) primers 1781.0_qF17 ATTACGAACCCACTACCTGAATTATTGTTACC Contig1781.0 tiling qPCR G (SEQ ID No: 134) primers 1781.0_qR17 AAACGTCCTGCAGGACAACGC (SEQ ID No: Contig1781.0 tiling qPCR 135) primers 1781.0_qF16 TTGATTGAAGTTTTAATTTGGTACTGGGC Contig1781.0 tiling qPCR (SEQ ID No: 136) primers 1781.0_qR16 TTGGATGCTGATCTGTTTTGTTTAGAAAG Contig1781.0 tiling qPCR (SEQ ID No: 137) primers 1781.0_qF15 TTGGGATTTCTTAACTGGATTTCTTTCTAAAC Contig1781.0 tiling qPCR (SEQ ID No: 138) primers 1781.0_qR15 CTGCTTAAATTAAGTACTTCTATGTTTGAAAT Contig1781.0 tiling qPCR TAATGTTC (SEQ ID No: 139) primers 1781.0_qF14 CAATTAAAACACGTTGAACATTAATTTCAAAC Contig1781.0 tiling qPCR ATAG (SEQ ID No: 140) primers 1781.0_qR14 TGAGGATCCAAGGTAAATTTCATACAATC Contig1781.0 tiling qPCR (SEQ ID No: 141) primers 1781.0_qF13 GACTGCATGTATATGCTAATGATTGTATGAAA Contig1781.0 tiling qPCR TTTAC (SEQ ID No: 142) primers 1781.0_qR13 AGTGGCATTTCCAAGGAAACATTAATAC Contig1781.0 tiling qPCR (SEQ ID No: 143) primers 1781.0_qF12 CAGTGTTTCCCTTTGTGTAAATGGG (SEQ ID Contig1781.0 tiling qPCR No: 144) primers 1781.0_qR12 TCAGTGGATAAACTAGCCTAAGGAAACAC Contig1781.0 tiling qPCR (SEQ ID No: 145) primers 1781.0_qF11 TTTTACAGACTGGACACAGTAGTGTTTCC Contig1781.0 tiling qPCR (SEQ ID No: 146) primers 1781.0_qR11 CCAGTGGTATCAACATGCGGTCATC (SEQ ID Contig1781.0 tiling qPCR No: 147) primers 1781.0_qF10 GATATATACACTCCCAGCAGTAAAGATGACC Contig1781.0 tiling qPCR (SEQ ID No: 148) primers 1781.0_qR10 GAATAGGCTCACTCTAAATTCGAGTGC (SEQ Contig1781.0 tiling qPCR ID No: 149) primers 1781.0_qF9 ATTCGCTAGGTCTAAGCAAATATTGCAC Contig1781.0 tiling qPCR (SEQ ID No: 150) primers 1781.0_qR9 TAAATAGCCAAAACAACCAATAAAATTAACAA Contig1781.0 tiling qPCR TAACCTC (SEQ ID No: 151) primers 1781.0_qF8 CTTTTTGAGGGCGAGGTTATTGTTAATTTTAT Contig1781.0 tiling qPCR TG (SEQ ID No: 152) primers 1781.0_qR8 GATCCATTAATTACAGAAATAAATAATAGGCA Contig1781.0 tiling qPCR GCATA (SEQ ID No: 153) primers 1781.0_qF7 ATATTGCCTGAATTATTATGCTGCCTATTATT Contig1781.0 tiling qPCR TATT (SEQ ID No: 154) primers 1781.0_qR7 AAATGTGCACCGTCATCAAATACC (SEQ ID Contig1781.0 tiling qPCR No: 155) primers 1781.0_qF6 GGATCACTATAATCATCTGGATGACTATTGG Contig1781.0 tiling qPCR (SEQ ID No: 156) primers 1781.0_qR6 AAGTGTAATGTAGTTTCAATGGTAGTGATGT Contig1781.0 tiling qPCR G (SEQ ID No: 157) primers 1781.0_qF5 TGACTTCTTCCAGTGGATTCACATC (SEQ ID Contig1781.0 tiling qPCR No: 158) primers 1781.0_qR5 GCCAATTAATTCATTTGTTCGTAGAGATATGT Contig1781.0 tiling qPCR AA (SEQ ID No: 159) primers 1781.0_qF4 CACTTTATAATAAATAAGAATTATTACATATCT Contig1781.0 tiling qPCR CTACGAACAA (SEQ ID No: 160) primers 1781.0_qR4 CTCACCAGTAATTTGCAGACACC (SEQ ID Contig1781.0 tiling qPCR No: 161) primers 1781.0_qF3 GGCTGACTGGGGTTGAGTTAATC (SEQ ID Contig1781.0 tiling qPCR No: 162) primers 1781.0_qR3 AATATAAACAAAATGGAATATACAAAACTTGA Contig1781.0 tiling qPCR ATAAGAAATAG (SEQ ID No: 163) primers 1781.0_qF2 GAGACTGAGGATCTATTTCTTATTCAAGTTTT Contig1781.0 tiling qPCR G (SEQ ID No: 164) primers 1781.0_qR2 ATTAATACATTATTAACTTAAATATAAATATTT Contig1781.0 tiling qPCR AAAGAATTATGAACAATAAT (SEQ ID primers No: 165) 1781.0_qF1 CATTTTGTTTATATTATTGTTCATAATTCTTTA Contig1781.0 tiling qPCR AATATTTATATTTAAGTTAAT(SEQ ID primers No: 166) 1781.0_qR1 ACAAGATAACATTGCTAATTTTCAATAAATTA Contig1781.0 tiling qPCR AATTAATACATT (SEQ ID No: 167) primers 1781.0_F CCCCAAAACCCCAAAACCCCACTAGTCTTAA Primer pair for amplifying ATATGAGAAAGATGATTTGAATAAG (SEQ ID chromosome, to be added to No: 168) mini-genome 1781.0_R CCCCAAAACCCCAAAACCCCACAAGATAACA TTGCTAATTTTCAATAAATTAAAT (SEQ ID No: 169) 15118.0_F CCCCAAAACCCCAAAACCCCGATTTATGAAA Primer pair for amplifying GTGCTGTATTATTAAGGAATG (SEQ ID No: chromosome, to be added to 170) mini-genome 15118.0_R CCCCAAAACCCCAAAACCCCATTATTCCTAC TTTTAGCTATATTAGAAATTCG (SEQ ID No: 171) 1339.1_F CCCCAAAACCCCAAAACCCCATGATGATACA Primer pair for amplifying TAGATTCATTAAAATAAAAAAAAG (SEQ ID chromosome, to be added to No: 172) mini-genome 1339.1_R CCCCAAAACCCCAAAACCCCTTAGATGAATT AAATAAAGAATTCAAATAAATAC (SEQ ID No: 173) 20718.0_F CCCCAAAACCCCAAAACCCCATGAATCTGAA Primer pair for amplifying ATCGGGCAGTTGAATACG (SEQ ID chromosome, to be added to No: 174) mini-genome 20718.0_R CCCCAAAACCCCAAAACCCCATTTATCATAAT TATAGAGAAGATAGTGATGC (SEQ ID No: 175) 20822.0_F CCCCAAAACCCCAAAACCCCATGAGAGTTTG Primer pair for amplifying TGAAAAATTAAGTTTG (SEQ ID No: chromosome, to be added to 176) mini-genome 20822.0_R CCCCAAAACCCCAAAACCCCTATATTAAATAT CAAGAAAAAGTAAAAAGACAG (SEQ ID No: 177) 21162.0_F CCCCAAAACCCCAAAACCCCAAGTCTCATTT Primer pair for amplifying TGGTTAGTGATGTTTGGATTG (SEQ ID No: chromosome, to be added to 178) mini-genome 21162.0_R CCCCAAAACCCCAAAACCCCGTATGATCGAT GAATACAAAATCAAGTTGGAAG (SEQ ID No: 179) 11991.0_F CCCCAAAACCCCAAAACCCCACTTAAAAGGA Primer pair for amplifying TTGCATGATTGTAAGGGAAATGTG (SEQ ID chromosome, to be added to No: 180) mini-genome 11991.0_R CCCCAAAACCCCAAAACCCCAATAATCGCAC TTACATTATATCTGGAGAAATG (SEQ ID No: 181) 5079.0_F CCCCAAAACCCCAAAACCCCTTCTACTAAATT Primer pair for amplifying TCATTGATTTTTTTCAATTTC (SEQ ID chromosome, to be added to No: 182) mini-genome 5079.0_R CCCCAAAACCCCAAAACCCCATTTGATAGAA TAGAAGAGAAATTATGGAATG (SEQ ID No: 183) 13665.0_F CCCCAAAACCCCAAAACCCCAAGTATAAATA Primer pair for amplifying AGGGAGTTGATATATAATATACTT (SEQ ID chromosome, to be added to No: 184) mini-genome 13665.0_R CCCCAAAACCCCAAAACCCCATGAGAATTCC TATTCAAAAATGAAAAAGTAGATTG (SEQ ID No: 185) 22365.0_F CCCCAAAACCCCAAAACCCCATAAGGTAGTA Primer pair for amplifying TATTTTTATTAAGGATTGGAAATTA (SEQ ID chromosome, to be added to No: 186) mini-genome 22365.0_R CCCCAAAACCCCAAAACCCCATAAGACTAAA TTTATTGAAATTATCTTGTTAATAG (SEQ ID No: 187) 21620.0_F CCCCAAAACCCCAAAACCCCTTGAGCCAATA Primer pair for amplifying CTGAAAAGGATGATAGTGAATAGTG (SEQ ID chromosome, to be added to No: 188) mini-genome 21620.0_R CCCCAAAACCCCAAAACCCCTCATTTTTTAAA TTGGATAGTAAGAAAAATTATAATAAAG (SEQ ID No: 189) 15049.0_F CCCCAAAACCCCAAAACCCCAAGGAATAAAA Primer pair for amplifying TTCAATTCCAAAATGTAAGGTGAG (SEQ ID chromosome, to be added to No: 190) mini-genome 15049.0_R CCCCAAAACCCCAAAACCCCGTTAAAAGAAC CAAGTGATATATTATAAGCCA (SEQ ID No: 191) 16562.0_F CCCCAAAACCCCAAAACCCCTTTATCAATTAT Primer pair for amplifying AAATAAAAAGTTTTAAGTCTATTTTTAA (SEQ chromosome, to be added to ID No: 192) mini-genome 16562.0_R CCCCAAAACCCCAAAACCCCATAAGACAAAT GCAACTTTATAAAGTAAATAAATTATC (SEQ ID No: 193) 22360.0_F CCCCAAAACCCCAAAACCCCAATGCAACATT Primer pair for amplifying TACTTTTAACATTAGAGATTATC (SEQ ID chromosome, to be added to No: 194) mini-genome 22360.0_R CCCCAAAACCCCAAAACCCCATAAGAGCAAA AGTTAATATAAAAATTCAAGGTG (SEQ ID No: 195) 15836.0_F CCCCAAAACCCCAAAACCCCGATTTGCACAG Primer pair for amplifying TTAATTTGAATTTGGTATTTG (SEQ ID No: chromosome, to be added to 196) mini-genome 15836.0_R CCCCAAAACCCCAAAACCCCTCATTTTTAGTA TTTTAAATATCATTTAGTTTTAAGTAA (SEQ ID No: 197) 2324.0_F CCCCAAAACCCCAAAACCCCTTGATTGATTC Primer pair for amplifying CTGAATACAAATGAAATAATATAAAG (SEQ ID chromosome, to be added to No: 198) mini-genome 2324.0_R CCCCAAAACCCCAAAACCCCAAGACCAAAAT AAAGAGGAATAATGAGAAGTAC (SEQ ID No: 199) 22404.0_F CCCCAAAACCCCAAAACCCCATGTAGAATTA Primer pair for amplifying ATATGAGAACATCATTTTTTAAGC (SEQ ID chromosome, to be added to No: 200) mini-genome 22404.0_R CCCCAAAACCCCAAAACCCCATAATGTAAGA AATCTGATACAATAGAGAGATAAAC (SEQ ID No: 201) 15403.0_F CCCCAAAACCCCAAAACCCCGAATGGAAAAT Primer pair for amplifying TTGTATGAAGTTCAGAGAGAAAG (SEQ ID chromosome, to be added to No: 202) mini-genome 15403.0_R CCCCAAAACCCCAAAACCCCATAAGATTATC AGTTATAAAAATTGATAGGGGATG (SEQ ID No: 203) 17795.0_F CCCCAAAACCCCAAAACCCCATCATACGATA Primer pair for amplifying TCTTAAGTGTTGATCTGAATTAAAT (SEQ ID chromosome, to be added to No: 204) mini-genome 17795.0_R CCCCAAAACCCCAAAACCCCGTTAGGTTTAA GAGTAGAAATAAAAGGAGATAAG (SEQ ID No: 205) 11141.0_F CCCCAAAACCCCAAAACCCCTCTCACTATCT Primer pair for amplifying TTTGTAAAAAGTTGGTAGAT (SEQ ID chromosome, to be added to No: 206) mini-genome 11141.0_R CCCCAAAACCCCAAAACCCCGTTGGTTTAGA ATAAAGAATTGTATTAACCAAATTTAT (SEQ ID No: 207) 22342.0_F CCCCAAAACCCCAAAACCCCGTGAATTAAAA Primer pair for amplifying TATAAACGAATAAGATATAAAGATTG (SEQ ID chromosome, to be added to No: 208) mini-genome 22342.0_R CCCCAAAACCCCAAAACCCCTTAATTACTGA ATTGTTTATTATAAGATTATAAG (SEQ ID No: 209) 2240.0_F CCCCAAAACCCCAAAACCCCGTAATGAATAA Primer pair for amplifying ATTGTAAAGGTAAATTGCAA (SEQ ID chromosome, to be added to No: 210) mini-genome 2240.0_R CCCCAAAACCCCAAAACCCCAATGGCAAACA TTTAAAATAAATATTAATATAAATTAC (SEQ ID No: 211) 3531.0_F CCCCAAAACCCCAAAACCCCTAAAAGGAAAA Primer pair for amplifying CAAATAGAAGAAACTGAA (SEQ ID No: chromosome, to be added to 212) mini-genome 3531.0_R CCCCAAAACCCCAAAACCCCATTTGGATATT ATGATTAGCAGTTTAGTG (SEQ ID No: 213) 4701.0_F CCCCAAAACCCCAAAACCCCTTTAAATAAAAA Primer pair for amplifying TCGCATGAATTAAATGCAAG (SEQ ID chromosome, to be added to No: 214) mini-genome 4701.0_R CCCCAAAACCCCAAAACCCCTAGGTAAATGC AAATTGGAGAATTTCCAATAG (SEQ ID No: 215) 20883.0_F CCCCAAAACCCCAAAACCCCATATTAAGAAT Primer pair for amplifying TGTGTAATTTTTGAGTAAATTG (SEQ ID No: chromosome, to be added to 216) mini-genome 20883.0_R CCCCAAAACCCCAAAACCCCATTTAGTAGAA TCTTCAATAAATAAGCGTTATTG (SEQ ID No: 217) 15191.0_F CCCCAAAACCCCAAAACCCCTAGCATTAAAT Primer pair for amplifying TTGTAAAAAGAATGAAATTTAATAT (SEQ ID chromosome, to be added to No: 218) mini-genome 15191.0_R CCCCAAAACCCCAAAACCCCAATATACATGA TTTTAGATAAACAACAAATAAT (SEQ ID No: 219) 19342.0_F CCCCAAAACCCCAAAACCCCATCAAGAATGG Primer pair for amplifying ATTAGAATTTTTAATGCTTTGC (SEQ ID No: chromosome, to be added to 220) mini-genome 19342.0_R CCCCAAAACCCCAAAACCCCGAGGAACTAG GGATTACTCATTTTACTTCAG (SEQ ID No: 221) 15245.0_F CCCCAAAACCCCAAAACCCCATGCATGTAAT Primer pair for amplifying TTTCTGTCAAAATTGAGTAAATAG (SEQ ID chromosome, to be added to No: 222) mini-genome 15245.0_R CCCCAAAACCCCAAAACCCCGTAAGCTAAAT AAGTAGACTAAATAGGTAG (SEQ ID No: 223) 6109.0_F CCCCAAAACCCCAAAACCCCAACCGCAAATA Primer pair for amplifying GAATATATAAAGGATAATTTA (SEQ ID No: chromosome, to be added to 224) mini-genome 6109.0_R CCCCAAAACCCCAAAACCCCGAAGTACTAAA AATAAAAAGTAAAGTATTAAAATAAAATC (SEQ ID No: 225) 22610.0_F CCCCAAAACCCCAAAACCCCGTAGACAGATT Primer pair for amplifying TTCCAGTTTATAGCTGTGTTTG (SEQ ID No: chromosome, to be added to 226) mini-genome 22610.0_R CCCCAAAACCCCAAAACCCCTTTATGAATTTT CTTAAATCTGTAAATAAATAAAATAAT (SEQ ID No: 227) 11875.0_F CCCCAAAACCCCAAAACCCCGTATGTTAATT Primer pair for amplifying TTATGCTTTAAATGATAGTTTA (SEQ ID No: chromosome, to be added to 228) mini-genome 11875.0_R CCCCAAAACCCCAAAACCCCTGGATTCCATT TTGAAGAATAATTTATTAAC (SEQ ID No: 229) 15329.0_F CCCCAAAACCCCAAAACCCCTTGTTTCGATT Primer pair for amplifying ATATTCAAAATAGGAAATTTAG (SEQ ID No: chromosome, to be added to 230) mini-genome 15329.0_R CCCCAAAACCCCAAAACCCCATGAATTTCAA TAACTTTTTATGAAAATGAATTTA (SEQ ID No: 231) 20179.0_F CCCCAAAACCCCAAAACCCCTAGGAAGAAAA Primer pair for amplifying TCTTGTGTGCAATTTGAGATTAAC (SEQ ID chromosome, to be added to No: 232) mini-genome 20179.0_R CCCCAAAACCCCAAAACCCCTTGATAAAAAC ATAGATTAAATACTAGTGTATAAA (SEQ ID No: 233) 9936.0_F CCCCAAAACCCCAAAACCCCATATGGAATAT Primer pair for amplifying TTAATTTGATTTAAATGAAACGAAATA (SEQ chromosome, to be added to ID No: 234) mini-genome 9936.0_R CCCCAAAACCCCAAAACCCCTTGTAACAGTA AATAGAATATTTTAATTACCAAAAC (SEQ ID No: 235) 16267.0_F CCCCAAAACCCCAAAACCCCTCATTTTAGAA Primer pair for amplifying TTATCTGTACTTAATTATTTTG (SEQ ID No: chromosome, to be added to 236) mini-genome 16267.0_R CCCCAAAACCCCAAAACCCCATGAGCATGTT ATTTTACTTCATTAGTCAATTTG (SEQ ID No: 237) 4488.0_F CCCCAAAACCCCAAAACCCCATGAAATGAAT Primer pair for amplifying TCTAAGATTGAATTGCATG (SEQ ID chromosome, to be added to No: 238) mini-genome 4488.0_R CCCCAAAACCCCAAAACCCCAGAAGAGATCA ATAAATTGAGAAGGAATTG (SEQ ID No: 239) 8551.0_F CCCCAAAACCCCAAAACCCCGTGTTACAATT Primer pair for amplifying TGCGTTTGAAATAGTTGGTTGATA (SEQ ID chromosome, to be added to No: 240) mini-genome 8551.0_R CCCCAAAACCCCAAAACCCCATATGGTAAAA ATTGAAGAAAGAAATTCAAGAGAA (SEQ ID No: 241) 11746.0_F CCCCAAAACCCCAAAACCCCGTATTGATGAT Primer pair for amplifying AAAATTGTATACAAGTTGATAG (SEQ ID No: chromosome, to be added to 242) mini-genome 11746.0_R CCCCAAAACCCCAAAACCCCTAGATGCTTAA TTATTAAGAAGATTCTGGAATG (SEQ ID No: 243) 22291.0_F CCCCAAAACCCCAAAACCCCATAAACCAATG Primer pair for amplifying TAATTAATTTATTGGGTGTGTTG (SEQ ID chromosome, to be added to No: 244) mini-genome 22291.0_R CCCCAAAACCCCAAAACCCCTTAGATTAAATT TAGAGAGTTATAGAAATGTAGTAAAT (SEQ ID No: 245) 17535.0_F CCCCAAAACCCCAAAACCCCATCTCAATTTAT Primer pair for amplifying AAAATCAGAATAAGAGATTGTC (SEQ ID No: chromosome, to be added to 246) mini-genome 17535.0_R CCCCAAAACCCCAAAACCCCAGAATAAAACA ACTGAAGTAAATATGAGTTAC (SEQ ID No: 247) 15372.0_F CCCCAAAACCCCAAAACCCCTTTCAAATATAA Primer pair for amplifying AATAAACAGAAGAATGGCAAACG (SEQ ID chromosome, to be added to No: 248) mini-genome 15372.0_R CCCCAAAACCCCAAAACCCCAAATTCAATATT AAATGAAATAATTTTCAAAAGTG (SEQ ID No: 249) 13537.0_F CCCCAAAACCCCAAAACCCCATGAGATCAAA Primer pair for amplifying TTTTTTTATTAAAATTCTTC (SEQ ID chromosome, to be added to No: 250) mini-genome 13537.0_R CCCCAAAACCCCAAAACCCCTTGGATTCATA TTTTTGTTTAAGGCTTAGATA (SEQ ID No: 251) 22613.0_F CCCCAAAACCCCAAAACCCCATTAGAAAAGA Primer pair for amplifying GGATTTCAATAAAAGCAAATAT (SEQ ID No: chromosome, to be added to 252) mini-genome 22613.0_R CCCCAAAACCCCAAAACCCCATCGATTTATT ATTGTTGAATTTAAAAGTATTGAA (SEQ ID No: 253) 12585.0_F CCCCAAAACCCCAAAACCCCGAGAGGTTTGA Primer pair for amplifying TAAGTAGAATTAGTAAAATCTATAAAG (SEQ chromosome, to be added to ID No: 254) mini-genome 12585.0_R CCCCAAAACCCCAAAACCCCATTAGTACTAT TTTCATAGATCTATGTATAAATTGAA (SEQ ID No: 255) 5317.0_F CCCCAAAACCCCAAAACCCCAATGGAAAGAT Primer pair for amplifying AAACAGATTTTAATTTGGAAATAAAAT (SEQ chromosome, to be added to ID No: 256) mini-genome 5317.0_R CCCCAAAACCCCAAAACCCCTTTAAGCAGTA TTTCTAAAATGTTGATGAAATAAAAAT (SEQ ID No: 257) 17894.0_F CCCCAAAACCCCAAAACCCCATAAGATAAAA Primer pair for amplifying TTTAACGAAAAAAAGTTAAGTC (SEQ ID No: chromosome, to be added to 258) mini-genome 17894.0_R CCCCAAAACCCCAAAACCCCATAAGATGAAA TATAGAGATAATTGAGCCTA (SEQ ID No: 259) 3513.0_F CCCCAAAACCCCAAAACCCCAATTACATATTA Primer pair for amplifying ATGTACTTATGATAGAATG (SEQ ID chromosome, to be added to No: 260) mini-genome 3513.0_R CCCCAAAACCCCAAAACCCCTAATGATCAAA TAACCTGAGTTAAAGAAG (SEQ ID No: 261) 16420.0_F CCCCAAAACCCCAAAACCCCAAATTATGAAA Primer pair for amplifying ATAGACACTAATTGGATGTTC (SEQ ID No: chromosome, to be added to 262) mini-genome 16420.0_R CCCCAAAACCCCAAAACCCCTGATTCGTCAT ATGAAATTGAAAAGGAGTAAAT (SEQ ID No: 263) 1084.1_F CCCCAAAACCCCAAAACCCCAGCGCCATGAA Primer pair for amplifying TCTGATGCATTTATTTTAAG (SEQ ID chromosome, to be added to No: 264) mini-genome 1084.1_R CCCCAAAACCCCAAAACCCCGTAGATCATTT ATGTAAAAGATTTTGAGAGATG (SEQ ID No: 265) 22651.0_F CCCCAAAACCCCAAAACCCCATACAATTATTA Primer pair for amplifying TAAATGAAAAAGCGCACTAATC (SEQ ID No: chromosome, to be added to 266) mini-genome 22651.0_R CCCCAAAACCCCAAAACCCCATAGTTACTAT GAAAGGACTGGTACATAGAAATAATAG (SEQ ID No: 267) 8670.0_F CCCCAAAACCCCAAAACCCCTTAAGTCAATA Primer pair for amplifying TCTAAATCAAATATTAGTAGTATAAT (SEQ ID chromosome, to be added to No: 268) mini-genome 8670.0_R CCCCAAAACCCCAAAACCCCGTCATATGGTT TTATAAAATAAAATTGAGATTTTTTTG (SEQ ID No: 269) 19107.0_F CCCCAAAACCCCAAAACCCCATAAGGATAAA Primer pair for amplifying TTCTATCATATAAGTGGAAGTGC (SEQ ID chromosome, to be added to No: 270) mini-genome 19107.0_R CCCCAAAACCCCAAAACCCCATTCTTGAATA TTGATTATGCATATTGTGTAAAATAG (SEQ ID No: 271) 21021.0_F CCCCAAAACCCCAAAACCCCAAGCGTTGAAT Primer pair for amplifying TTTTTATAATATATGATAAAC (SEQ ID chromosome, to be added to No: 272) mini-genome 21021.0_R CCCCAAAACCCCAAAACCCCTTAATGCCAAT AAACAGATGAAAGTAGAGTTATAG (SEQ ID No: 273) 15004.0_F CCCCAAAACCCCAAAACCCCATAGAGAGTGT Primer pair for amplifying TTTATTGAAGGACAGAGAATATTG (SEQ ID chromosome, to be added to No: 274) mini-genome 15004.0_R CCCCAAAACCCCAAAACCCCGAGCGTAAGAA ATATTCTTAGATAAATGGAAACTG (SEQ ID No: 275) 18789.0_F CCCCAAAACCCCAAAACCCCATGGCAATATC Primer pair for amplifying TTTGCGTGTTTCTGGC (SEQ ID chromosome, to be added to No: 276) mini-genome 18789.0_R CCCCAAAACCCCAAAACCCCATAAGAATAAA TTAAAGAAGATTTGAGAAAGATATGC (SEQ ID No: 277) 1335.1_F CCCCAAAACCCCAAAACCCCAAATGCTAAAA Primer pair for amplifying ATAATGAAAAATCTGAGGG (SEQ ID chromosome, to be added to No: 278) mini-genome 1335.1_R CCCCAAAACCCCAAAACCCCTAATGACAGGT TTAGTAATAATTTAGCTG (SEQ ID No: 279) 17286.0_F CCCCAAAACCCCAAAACCCCACGACTTAACA Primer pair for amplifying TTGCTGTTAAATATTCAGAAAT (SEQ ID No: chromosome, to be added to 280) mini-genome 17286.0_R CCCCAAAACCCCAAAACCCCTAAAATTGGAA AGGGGCAAATTTGCTTATGA (SEQ ID No: 281) 7278.0_F CCCCAAAACCCCAAAACCCCATGAGTAATAT Primer pair for amplifying ATACAAATTTTAAATGTATTTTGATTTA (SEQ chromosome, to be added to ID No: 282) mini-genome 7278.0_R CCCCAAAACCCCAAAACCCCATTGAGTGAGT ATTTTTATATTTATTGCGAGTTA (SEQ ID No: 283) 7752.0_F CCCCAAAACCCCAAAACCCCACAATAGGCAT Primer pair for amplifying ATTTAATAATTAATTGTTAAAG (SEQ ID No: chromosome, to be added to 284) mini-genome 7752.0_R CCCCAAAACCCCAAAACCCCACTCATTATAT AAGGCTGAAAAAATCAGAGG (SEQ ID No: 285) 244.1_F CCCCAAAACCCCAAAACCCCTAAATGTAAGA Primer pair for amplifying GTAAACTATCATATGAAAG (SEQ ID chromosome, to be added to No: 286) mini-genome 244.1_R CCCCAAAACCCCAAAACCCCATAATGCGAAA TATTCATCAGAGTAAATAATG (SEQ ID No: 287) 20383.0_F CCCCAAAACCCCAAAACCCCATACGTCATGA Primer pair for amplifying TTATAAGATTATTATAGAATGCTTAC (SEQ ID chromosome, to be added to No: 288) mini-genome 20383.0_R CCCCAAAACCCCAAAACCCCTCTTGTAAAAT AATAAGTTTAAGAAATTGAATTTAG (SEQ ID No: 289) 331.1_F CCCCAAAACCCCAAAACCCCATAATATCAAA Primer pair for amplifying TTAATGAATATTTATCAATTTTATTAAT (SEQ chromosome, to be added to ID No: 290) mini-genome 331.1_R CCCCAAAACCCCAAAACCCCCCCTAATGTCC ATAATTTATGTATCAAATAAGG (SEQ ID No: 291) 22208.0_F CCCCAAAACCCCAAAACCCCATGATGGTGGA Primer pair for amplifying GGAGTGAAGATAAATTAGAATG (SEQ ID No: chromosome, to be added to 292) mini-genome 22208.0_R CCCCAAAACCCCAAAACCCCAAAGTGCAATA AAAAGAGTGAAAATAAATTTTTG (SEQ ID No: 293) 21398.0_F CCCCAAAACCCCAAAACCCCATATACCAATG Primer pair for amplifying TTAAAAATGAATATTGATATAGAATAG (SEQ chromosome, to be added to ID No: 294) mini-genome 21398.0_R CCCCAAAACCCCAAAACCCCATAATACAAAG TAAAATTGTTTTTTATAGTTCATAA (SEQ ID No: 295) 11890.0_F CCCCAAAACCCCAAAACCCCACATAGTGAAT Primer pair for amplifying GAATTAATGAATAAGTTTGAG (SEQ ID No: chromosome, to be added to 296) mini-genome 11890.0_R CCCCAAAACCCCAAAACCCCGTGATAATAAA TTCCTGAGTATATAGTTTAAGAAG (SEQ ID No: 297) 13521.0_F CCCCAAAACCCCAAAACCCCGTGATTGCATT Primer pair for amplifying TTTTTGCGAAATATTTGC (SEQ ID No: chromosome, to be added to 298) mini-genome 13521.0_R CCCCAAAACCCCAAAACCCCTGAGTTCTCAT GTAATAAAAGAATCCATG (SEQ ID No: 299) 3511.0_F CCCCAAAACCCCAAAACCCCATGATGCTACA Primer pair for amplifying AAAACGCTATATAATCTATAAC (SEQ ID No: chromosome, to be added to 300) mini-genome 3511.0_R CCCCAAAACCCCAAAACCCCTTGAACTTTCA ATAGATGTTTGATTAAATTC (SEQ ID No: 301) 22209.0_F CCCCAAAACCCCAAAACCCCAAAGATATGTG Primer pair for amplifying GCTGGATTTTAAAATATGGTTG (SEQ ID No: chromosome, to be added to 302) mini-genome 22209.0_R CCCCAAAACCCCAAAACCCCAAGACTAATGA ATTTGAGAATTATAAAATAATGAATC (SEQ ID No: 303) 18924.0_F CCCCAAAACCCCAAAACCCCATCAACTTTAA Primer pair for amplifying TTCATTGTAGGAATTAAAGATGTAATAC (SEQ chromosome, to be added to ID No: 304) mini-genome 18924.0_R CCCCAAAACCCCAAAACCCCGTGAGAACAAA TAATAATAAAAATAAAGGAATTAA (SEQ ID No: 305) 14977.0_F CCCCAAAACCCCAAAACCCCAATTCTTTATCT Primer pair for amplifying GAATTAGATAAGAATTCATAAGC (SEQ ID chromosome, to be added to No: 306) mini-genome 14977.0_R CCCCAAAACCCCAAAACCCCGTGAGTATGCA ATAGATTGTTAATTAAATTTG (SEQ ID No: 307) 18694.0_F CCCCAAAACCCCAAAACCCCAAGTTGCTAAA Primer pair for amplifying AATAGTTGATAGCAACAAGTTAT (SEQ ID chromosome, to be added to No: 308) mini-genome 18694.0_R CCCCAAAACCCCAAAACCCCTGGATGTGTTT TTTTCCAAATTAATGAACAAAAATTAAA (SEQ ID No: 309) 13237.0_F CCCCAAAACCCCAAAACCCCAACATTCTAAA Primer pair for amplifying TTTCTTCTTTATAAGATTATTG (SEQ ID No: chromosome, to be added to 310) mini-genome 13237.0_R CCCCAAAACCCCAAAACCCCATCTAAACTAA TCTGAAACCAAAGATAGTATG (SEQ ID No: 311) 21338.0_F CCCCAAAACCCCAAAACCCCGTTATCCATAT Primer pair for amplifying ATACGTAAGCATTTTGCGATTG (SEQ ID No: chromosome, to be added to 312) mini-genome 21338.0_R CCCCAAAACCCCAAAACCCCGAAACCTATGC ATTATTTTTAAAGAAATATTAAATTAA (SEQ ID No: 313) 215.1_F CCCCAAAACCCCAAAACCCCTCGTACATTAA Primer pair for amplifying TAGTTGAAATTGCTTTTATTAAATTG (SEQ ID chromosome, to be added to No: 314) mini-genome 215.1_R CCCCAAAACCCCAAAACCCCGTAGTCTAAAA TAAATTTTATTTTGGGTTTTAA (SEQ ID No: 315) 13236.0_F CCCCAAAACCCCAAAACCCCGTTAAATGATA Primer pair for amplifying ATCATAGCAAAATTGCGGTAT (SEQ ID No: chromosome, to be added to 316) mini-genome 13236.0_R CCCCAAAACCCCAAAACCCCAAGGATAAATA TTGAAAGTAAATGTTCTAATTAATTTGC (SEQ ID No: 317) 16827.0_F CCCCAAAACCCCAAAACCCCAGAAATGAAAA Primer pair for amplifying GAATGATTTTTGAGGGGATTC (SEQ ID No: chromosome, to be added to 318) mini-genome 16827.0_R CCCCAAAACCCCAAAACCCCTAAAGGCAAAA GTCGATTTAAATGCTCAGTTTC (SEQ ID No: 319) 15136.0_F CCCCAAAACCCCAAAACCCCTTAAGGCTAAA Primer pair for amplifying ATACTTGTTTTACTAGAGAAC (SEQ ID No: chromosome, to be added to 320) mini-genome 15136.0_R CCCCAAAACCCCAAAACCCCATAAATCAAAT TAAATTGCATAACATGAAC (SEQ ID No: 321) 115.1_F CCCCAAAACCCCAAAACCCCAGAGGATGTAA Primer pair for amplifying ATTACAATAAATCGTAAAAAC (SEQ ID No: chromosome, to be added to 322) mini-genome 115.1_R CCCCAAAACCCCAAAACCCCTTCTAAAAAAT ATAAAGATAAATTGACGTC (SEQ ID No: 323) 21295.0_F CCCCAAAACCCCAAAACCCCATCCAGTTGAA Primer pair for amplifying ATCTAAAACAATTTTGTATATTTAAAG (SEQ chromosome, to be added to ID No: 324) mini-genome 21295.0_R CCCCAAAACCCCAAAACCCCTTAAGAGATTG CATTATAAATAAGATAGGATTC (SEQ ID No: 325) 16269.0_F CCCCAAAACCCCAAAACCCCATTGATTGATA Primer pair for amplifying AACTTGGAAGTTAAGAAAGATTTG (SEQ ID chromosome, to be added to No: 326) mini-genome 16269.0_R CCCCAAAACCCCAAAACCCCATGAATAACAG ATGGAATGCTTCAAGATATG (SEQ ID No: 327) 644.1_F CCCCAAAACCCCAAAACCCCAAATGTTAGTA Primer pair for amplifying TTTGAATTAAAGAGAGGTAAAAC (SEQ ID chromosome, to be added to No: 328) mini-genome 644.1_R CCCCAAAACCCCAAAACCCCTTATGAAAATG AAATGGTTTTGATTGGCTAATAA (SEQ ID No: 329) 5586.0_F CCCCAAAACCCCAAAACCCCATGAGTAAAAT Primer pair for amplifying TTAGCTTAAGTAATGTAAGAATC (SEQ ID chromosome, to be added to No: 330) mini-genome 5586.0_R CCCCAAAACCCCAAAACCCCATATATCAAAA TATCAACATTTTTTTGTGTGATTGTTAC (SEQ ID No: 331) 13085.0_F CCCCAAAACCCCAAAACCCCTTGATGAAATT Primer pair for amplifying TGAAAATGAATAGAGAGTAC (SEQ ID No: chromosome, to be added to 332) mini-genome 13085.0_R CCCCAAAACCCCAAAACCCCGTAATGCTACA TTTGCAAAAAAGTACAAACAG (SEQ ID No: 333) 13838.0_F CCCCAAAACCCCAAAACCCCGTAAGGCCAGA Primer pair for amplifying ATCAATGAATAAAAAGGTC (SEQ ID chromosome, to be added to No: 334) mini-genome 13838.0_R CCCCAAAACCCCAAAACCCCGAAAAGGGAG ATTTACAAAAATTTGTAGATGTTATATTG (SEQ ID No: 335) 1415.1_F CCCCAAAACCCCAAAACCCCATTGATCATTA Primer pair for amplifying ATAAAGAAGAATTGCTAATAT (SEQ ID No: chromosome, to be added to 336) mini-genome 1415.1_R CCCCAAAACCCCAAAACCCCAATGCGATGAA ATGTTTTTTATTATGAAAAG (SEQ ID No: 337) 19468.0_F CCCCAAAACCCCAAAACCCCAAGGAAGTTCA Primer pair for amplifying ATGCTATTTAGCAAATTAGG (SEQ ID chromosome, to be added to No: 338) mini-genome 19468.0_R CCCCAAAACCCCAAAACCCCTTGATTCAAAA TATGCACAAGATTAAAAATTCAC (SEQ ID No: 339) 20407.0_F CCCCAAAACCCCAAAACCCCATAAGAAAGAT Primer pair for amplifying AAGTTGCAATTAAATAATAAGG (SEQ ID No: chromosome, to be added to 340) mini-genome 20407.0_R CCCCAAAACCCCAAAACCCCATGAAGACAAG TCTGATGAAAATAGAATGG (SEQ ID No: 341) 19922.0_F CCCCAAAACCCCAAAACCCCATAGTCTTAAA Primer pair for amplifying ATTTTATACTATCATGAAATAATATTAAG (SEQ chromosome, to be added to ID No: 342) mini-genome 19922.0_R CCCCAAAACCCCAAAACCCCGTAAGTCTAAA GTTTAACAGTTTTTAGTAAATATC (SEQ ID No: 343) 20459.0_F CCCCAAAACCCCAAAACCCCTTATGCTAGTT Primer pair for amplifying GAGTGATTGAAAATATATTTGTGC (SEQ ID chromosome, to be added to No: 344) mini-genome 20459.0_R CCCCAAAACCCCAAAACCCCTTGACGTAGAA TAATGGGCTTATAGAAG (SEQ ID No: 345) 20493.0_F CCCCAAAACCCCAAAACCCCTTAATCAACTC Primer pair for amplifying ACTTTACCCACTAATCAAACAC (SEQ ID No: chromosome, to be added to 346) mini-genome 20493.0_R CCCCAAAACCCCAAAACCCCATATTTAAGAT ATACAGAAATATAGAGAATACAAC (SEQ ID No: 347) 9925.0_F CCCCAAAACCCCAAAACCCCATTGGATCAAT Primer pair for amplifying TTTGAAGAGAATTCATGGAAAAT (SEQ ID chromosome, to be added to No: 348) mini-genome 9925.0_R CCCCAAAACCCCAAAACCCCATCAGAAAAAA TATTTGAAAATTCGATAAAGC (SEQ ID No: 349) 22456.0_F CCCCAAAACCCCAAAACCCCATTTCACTTTAT Primer pair for amplifying TTATATATAGATTTGAAATTAAAGTT (SEQ ID chromosome, to be added to No: 350) mini-genome 22456.0_R CCCCAAAACCCCAAAACCCCAGTTGACATGT TATTTCCAAATTTTCATGGATA (SEQ ID No: 351) 17712.0_F CCCCAAAACCCCAAAACCCCATGATAACAGG Primer pair for amplifying AATATTTTATAAAATAGTTAAG (SEQ ID No: chromosome, to be added to 352) mini-genome 17712.0_R CCCCAAAACCCCAAAACCCCTCACTCTATGC AATAAATTTGTTGATATATT (SEQ ID No: 353) 11116.0_F CCCCAAAACCCCAAAACCCCTTAAAAAAAGA Primer pair for amplifying ATAGTTGGAATAAAAATGAATTT (SEQ ID chromosome, to be added to No: 354) mini-genome 11116.0_R CCCCAAAACCCCAAAACCCCAATAGATAAAG ATGCCTTTTTTAATAAGTATTTAAC (SEQ ID No: 355) 19275.0_F CCCCAAAACCCCAAAACCCCGAGAGGATAAA Primer pair for amplifying TTTATATGAAAATAAAAATAAAGC (SEQ ID chromosome, to be added to No: 356) mini-genome 19275.0_R CCCCAAAACCCCAAAACCCCATAAATAAGAA ATTTTAAGAATAACGGGCAAATTAG (SEQ ID No: 357) 21217.0_F CCCCAAAACCCCAAAACCCCTTGAATTTTAAA Primer pair for amplifying TAAACTTCTTTGTATGATTTAAATG (SEQ ID chromosome, to be added to No: 358) mini-genome 21217.0_R CCCCAAAACCCCAAAACCCCATAGATTACTT TTCAAAGAATTTCTTGACATTC (SEQ ID No: 359) 10537.0_F CCCCAAAACCCCAAAACCCCAAAGCAAAGAA Primer pair for amplifying ATCTGATGTTTTATTAGAAAAAGTG (SEQ ID chromosome, to be added to No: 360) mini-genome 10537.0_R CCCCAAAACCCCAAAACCCCATGAGATGATA ATATTGCCTTTTTGCATATAAT (SEQ ID No: 361) 22670.0_F CCCCAAAACCCCAAAACCCCATCCTTATACA Primer pair for amplifying AATTCAGAAAACTTAGCAAAT (SEQ ID No: chromosome, to be added to 362) mini-genome 22670.0_R CCCCAAAACCCCAAAACCCCGTGGAGAATTT TCTAAAGAATTTTCGGAAATTTG (SEQ ID No: 363) 1781.0_F CCCCAAAACCCCAAAACCCCACTAGTCTTAA PCR primers for amplifying ATATGAGAAAGATGATTTGAATAAG (SEQ ID synthetic chromosome 1 and 6 No: 364) in FIG. 5B 1781.0_R CCCCAAAACCCCAAAACCCCACAAGATAACA TTGCTAATTTTCAATAAATTAAAT (SEQ ID No: 365) 1781.0_Purple_F GTCAGTGGTCTCAGTATGAAATTTACCTTGG PCR primers for amplifying ATCCTCAGTGTTTCCCTTTGTG (SEQ ID No: purple DNA building block in 366) synthetic chromosomes 2-4 in 1781.0_Purple_R AACGCTCGGTCTCGCAGAAATAAATAATAGG FIG. 5B CAGCATAATAATTCAGG (SEQ ID No: 367) 1781.0_red_F GTCAGTGGTCTCTCCAGTGGATTCACATCAC PCR primers for amplifying TACCATTG (SEQ ID No: 368) red DNA building block in 1781.0_red_R CCCCAAAACCCCAAAACCCCACAAGATAACA synthetic chromosomes 2-4 TTGCTAATTTTCAATAAATTAAAT (SEQ ID in FIG. 5B No: 369) 1781.0_turquoise_F CCCCAAAACCCCAAAACCCCACTAGTCTTAA PCR primers for amplifying ATATGAGAAAGATGATTTGAATAAG (SEQ ID turquoise DNA building block No: 370) in synthetic chromosomes 2-4 1781.0_turquoise_R ACGCTCGGTCTCGATACAATCATTAGCATAT in FIG. 5B ACATGCAGTCTGCTTAAATTAAG (SEQ ID No: 371) DarkBlue_6mA_top TCTGTAATTAATGGATCACTATAATCATCTGG Oligos for annealing to make ATGACTATTGGTATTTGATGACGGTGCACAT blue DNA building block in TTGACTTCTT (SEQ ID No: 372) synthetic chromosomes 2-4 in DarkBlue_6mA_bottom ATTAATTACCTAGTGATATTAGTAGACCTACT FIG. 5B. Bold red nucleotides GATAACCATAAACTACTGCCACGTGTAAACT represent 6mA. GAAGAAGGTC (SEQ ID No: 373) 1781.0_red2_F AGCCTAGGTCTCGTTCTTTTTGAGGGCGAGG PCR primers for amplifying TTATTGTTAAT (SEQ ID No: 374) red DNA building block in 1781.0_red2_R CCCCAAAACCCCAAAACCCCACAAGATAACA synthetic chromosome 5 in T (SEQ ID No: 375) FIG. 5B 1781.0_orange_F TAGTCAGGTCTCTAGAATAGGCTCACTCTAA PCR primers for amplifying ATTCGAGTGCAAT (SEQ ID No: 376) orange DNA building block in 1781.0_orange_R TCTACTGGTCTCAGTATGAAATTTACCTTGGA synthetic chromosome 5 in FIG. TCCTCAGTGT (SEQ ID No: 377) 5B 1781.0_emerald_F ATCGTAGGTCTCAATACAATCATTAGCATATA PCR primers for amplifying CATGCAGT (SEQ ID No: 378) emerald DNA building block in 1781.0_emerald_R CCCCAAAACCCCAAAACCCCACTAGTCTTAA synthetic chromosome 5 in FIG. AT (SEQ ID No: 379) 5B 17535.0_F CCCCAAAACCCCAAAACCCCATCTCAATTTAT PCR primers for amplifying AAAATCAGAATAAGAGATTGTC (SEQ ID No: “buffer” chromosome 380) (Contig17535.0) for use in 17535.0_R CCCCAAAACCCCAAAACCCCAGAATAAAACA chromatin assembly ACTGAAGTAAATATGAGTTAC (SEQ ID No: 381) 12701assay_F AAGAAGAACTAGCCAGCTCTCACTCAGTTC PCR primers for assaying the (SEQ ID No: 382) presence of ectopic DNA 12701assay_R TGTCTATCTCATCAGGCTCATCAGCATAGG insertion in mta1 mutants (SEQ ID No: 383) 12701_firstround_T7_F AAGAAGAACTAGCCAGCTCTCACTCAGTTC PCR primers to generate DNA (SEQ ID No: 384) template for ssRNA in vitro 12701_firstround_T7_R CCTCTCTGCCCACTAAATTATTCTGACAGC transcription. This ssRNA is (SEQ ID No: 385) injected into Oxytricha cells to induce ectopic DNA retention in MTA1 gene. PCR product is amplified from Oxytricha gDNA of cell strain JRB310. The resulting PCR product is subjected to a second round of PCR amplification using primers “12701_secondround_T7_F” and “12701_secondround_T7_R”. The final, second round PCR product is then used for ssRNA in vitro transcription. 12701_secondround_T7_F CTACTTGATATAATACGACTCACTATAGGGAA PCR primers for second round TTCCTAAGGGGAGTGAAGCCAACAACAG amplification of DNA template, (SEQ ID No: 386) to be used for ssRNA in vitro 12701_secondround_T7_R TGTCTATCTCATCAGGCTCATCAGCATAGG transcription. Forward primer (SEQ ID No: 387) contains T7 promoter sequence, which is required for subsequent in vitro transcription. metGATC_F2 GTGCTATGCATTTTAAATTTATTCGCATTGAA PCR primers for amplification GA (SEQ ID No: 388) of DNA substrate for use in metGATC_R2 ATTCAGAATTTTAGTGTGTGGAGTATGATAGT 6mA methyltransferase assay A (SEQ ID No: 389) involving Tetrahymena nuclear noGATC2_F GGTCTATATTATTTTAGTATTCTTTCTATAAAT PCR primers for amplifying G (SEQ ID No: 390) 350 bp dsDNA substrate for noGATC2_R GTTACAAGAATATAAGAAAAGAAAGGGTGAA methyltransferase assays TAGG (SEQ ID No: 391) involving recombinant proteins (in FIGS. 2E, 2F, and 10H) T7noGATC2_F2 TAATACGACTCACTATAGGG PCR primers for amplifying GGTCTATATTATTTTAGTATTCTTTC (SEQ ID DNA ~350 bp dsDNA template No: 392) with T7 overhangs at one end, noGATC2_R GTTACAAGAATATAAGAAAAGAAAGGGTGAA for subsequent ssRNA TAGG (SEQ ID No: 393) production by in vitro transcription T7noGATC2_F2 TAATACGACTCACTATAGGG PCR primers for amplifying GGTCTATATTATTTTAGTATTCTTTC (SEQ ID DNA ~350 bp dsDNA template No: 394) with T7 overhangs at the 5′ T7noGATC2_R2 TAATACGACTCACTATAGGG and 3′ ends, for subsequent GTTACAAGAATATAAGAAAAG (SEQ ID No: dsRNA production by in vitro 395) transcription noGATC_F3 AACTTCTGTCATTACATTAAGCTTTAA (SEQ DNA oligonucleotides for use ID No: 396) in DNA methyltransferase noGATC_R3 TTAAAGCTTAATGTAATGACAGAAGTT (SEQ assays in FIGS. 2G, 10I, ID No: 397) 10J, 10K, 10L noGATC_F12 AACTTCTGTCATTAACTTAAGCTTTAA (SEQ ID No: 398) noGATC_R12 TTAAAGCTTAAGTTAATGACAGAAGTT (SEQ ID No: 399) noGATC_F13 AACTTCTGTACTTACATTAAGCTTTAA (SEQ ID No: 400) noGATC_R13 TTAAAGCTTAATGTAAGTACAGAAGTT (SEQ ID No: 401) noGATC_F14 AACTTCTGTACTTAACTTAAGCTTTAA (SEQ ID No: 402) noGATC_R14 TTAAAGCTTAAGTTAAGTACAGAAGTT (SEQ ID No: 403) noGATC_F1 AACTTCTGTCATTACATTAAGCTTTAAAAAAT TCAATTCCTTTTATT (SEQ ID No: 404) noGATC_R1 AATAAAAGGAATTGAATTTTTTAAAGCTTAAT GTAATGACAGAAGTT (SEQ ID No: 405) noGATC_F2 TGTCATTACATTAAGCTTTAAAAAATTCAATT CCT (SEQ ID No: 406) noGATC_R2 AGGAATTGAATTTTTTAAAGCTTAATGTAATG ACA (SEQ ID No: 407) noGATC_F3 AACTTCTGTCATTACATTAAGCTTTAA (SEQ ID No: 408) noGATC_R3 TTAAAGCTTAATGTAATGACAGAAGTT (SEQ ID No: 409) noGATC_F8 TATTAGAATTATGTTCTTCATGAAATT (SEQ ID No: 410) noGATC_R8 AATTTCATGAAGAACATAATTCTAATA (SEQ ID No: 411)

TABLE-US-00004 TABLE 3 Recombinant protein sequences. >MTA1 (manually curated from Tetrahymena DB gene ID: TTHERM_00704040) (SEQ ID No: 412) MSKAVNKKGLRPRKSDSILDHIKNKLDQEFLEDNENGEQSDEDYDQKS LNKAKKPYKKRQTQNGSELVISQQKTKAKASANNKKSAKNSQKLDEEE KIVEEEDLSPQKNGAVSEDDQQQEASTQEDDYLDRLPKSKKGLQGLLQ DIEKRILHYKQLFFKEQNEIANGKRSMVPDNSIPICSDVTKLNFQALI DAQMRHAGKMFDVIMMDPPWQLSSSQPSRGVAIAYDSLSDEKIQNMPI QSLQQDGFIFVWAINAKYRVTIKMIENWGYKLVDEITWVKKTVNGKIA KGHGFYLQHAKESCLIGVKGDVDNGRFKKNIASDVIFSERRGQSQKPE EIYQYINQLCPNGNYLEIFARRNNLHDNWVSIGNEL >MTA9 (manually curated from Tetrahymena DB gene ID: TTHERM_00301770) (SEQ ID No: 413) MAPKKQEQEPIRLSTRTASKKVDYLQLSNGKLEDFFDDLEEDNKPARN RSRSKKRGRKPLKKADSRSKTPSRVSNARGRSKSLGPRKTYPRKKNLS PDNQLSLLLKWRNDKIPLKSASETDNKCKVVNVKNIFKSDLSKYGANL QALFINALWKVKSRKEKEGLNINDLSNLKIPLSLMKNGILFIWSEKEI LGQIVEIMEQKGFTYIENFSIMFLGLNKCLQSINHKDEDSQNSTASTN NTNNEAITSDLTLKDTSKFSDQIQDNHSEDSDQARKQQTPDDITQKKN KLLKKSSVPSIQKLFEEDPVQTPSVNKPIEKSIEQVTQEKKFVMNNLD ILKSTDINNLFLRNNYPYFKKTRHTLLMFRRIGDKNQKLELRHQRTSD VVFEVTDEQDPSKVDTMMKEYVYQMIETLLPKAQFIPGVDKHLKMMEL FASTDNYRPGWISVIEK >p1 (manually curated from Tetrahymena DB gene ID: TTHERM_00161750) (SEQ ID No: 414) MSLKKGKFQHNQSKSLWNYTLSPGWREEEVKILKSALQLFGIGKWKKI MESGCLPGKSIGQIYMQTQRLLGQQSLGDFMGLQIDLEAVFNQNMKKQ DVLRKNNCIINTGDNPTKEERKRRIEQNRKIYGLSAKQIAEKLPKVKK HAPQYMTLEDIENEKFTNLEILTHLYNLKAEIVRRLAEQGETIAQPSI IKSLNNLNHNLEQNQNSNSSTETKVTLEQSGKKKYKVLAIEETELQNG PIATNSQKKSINGKRKNNRKINSDSEGNEEDISLEDIDSQESEINSEE IVEDDEEDEQIEEPSKIKKRKKNPEQESEEDDIEEDQEEDELVVNEEE IFEDDDDDEDNQDSSEDDDDDED >p2 (manually curated from Tetrahymena DB gene ID: TTHERM_00439330) (SEQ ID No: 415) MKKNSKSQNQPLDFTQYAKNMRKDLSNQDICLEDGALNHSYFLTKKGQ YWTPLNQKALQRGIELFGVGNWKEINYDEFSGKANIVELELRICMILG INDITEYYGKKISEEEQEEIKKSNIAKGKKENKLKDNIYQKLQQMQ
Sequences were manually curated by mapping RNaseq reads to reference gene annotations and verifying the accuracy of predicted exon boundaries.

Example 2

Epigenomic Profiles of Chromatin and Transcription in Oxytricha

[0203] We generated genome-wide in vivo maps of nucleosome positioning, transcription, and 6 mA in the macronuclei of asexually growing (vegetative) Oxytricha trifallax cells using Mnase sequencing (MNase-seq), poly(Ar RNA sequencing (RNA-seq), transcriptional start site sequencing (TSS-seq), and single-molecule real-time sequencing (SMRT-seq) (FIGS. 1A-1E). The smallest Oxytricha chromosome is only 430 bp in length, with a single well-positioned nucleosome. Strikingly, 6 mA is enriched in three consecutive nucleosome-depleted regions directly downstream of transcription start sites (TSSs; FIG. 1A). Each region contains varying levels of 6 mA (FIG. 1B), with the +1/+2 nucleosome linker being most densely methylated (Table 4). In general, highly transcribed chromosomes tend to bear more 6 mA, suggesting a positive role of this DNA modification in gene regulation (FIG. 1C). The majority of methylation marks are located within an ApT motif (FIGS. 1D and 1E). 6 mA occurs on sense and antisense strands with approximately equal frequency, indicating that the underlying methylation machinery does not function strand-specifically. Quantitative LC-MS/MS analysis confirmed the presence of 6 mA in Oxytricha (FIGS. 8A and 8B; see Example 1).

TABLE-US-00005 TABLE 4 Descriptive statistics of 6mA distribution in the genome. Number of 6mA sites Oxytricha Tetrahymena Standard Standard Minimum Maximum Median Mean Deviation Minimum Maximum Median Mean Deviation Methyl 0 14 2 2.03 2.27 0 27 10 9.66 6.10 Cluster 1 Methyl 0 24 6 5.99 4.24 0 26 9 8.78 5.78 Cluster 2 Methyl 0 16 2 2.49 2.91 0 25 5 5.75 5.53 Cluster 3

[0204] Properties of 6 mA distribution in nucleosome linkers. In Oxytricha, methyl cluster 1=between 5′ chromosome end and +1 nucleosome; methyl cluster 2=between +1 and +2 nucleosome; methyl cluster 3=between +2 and +3 nucleosome. In Tetrahymena, methyl cluster 1=between +1 and +2 nucleosome; methyl cluster 2=between +2 and +3 nucleosome; methyl cluster 3=between +3 and +4 nucleosome. Consensus +1/+2/+3/+4 nucleosome positions: 193, 402, 618, 837 bp downstream of Oxytricha 5′ chromosome ends; 112, 304, 497, 698 bp downstream of Tetrahymena TSSs.

Example 3

Purification and Reconstitution of the Ciliate 6 mA Methyltransferase, MTA1c

[0205] To uncover the functions of 6 mA in vivo, we set out to identify and disrupt putative 6 mA methytransferases (MTases). The Oxytricha genome encodes a large number of candidate methyltransferases (Table 5), rendering it impractical to test gene function, one at a time or in combination. To identify the ciliate 6 mA MTase, we undertook a biochemical approach by fractionating nuclear extracts and identifying candidate proteins that co-purified with DNA methylase activity. The organism of choice for this experiment was Tetrahymena thermophila, a ciliate that divides significantly faster than Oxytricha (˜2 h versus 18 h; Cassidy-Hanley, 2012; Laughlin et al., 1983). This faster growth time rendered it feasible to culture large amounts of Tetrahymena cells for nuclear extract preparation. Tetrahymena and Oxytricha exhibit similar genomic localization and 6 mA abundance (FIGS. 8A-8B and 9A-9F). We thus reasoned that the enzymatic machinery responsible for 6 mA deposition is conserved between Tetrahymena and Oxytricha, and that Tetrahymena could serve as a tractable biochemical system for identifying the ciliate 6 mA MTase.

[0206] We prepared nuclear extracts from log-phase Tetrahymena cells, since 6 mA could be readily detected at this developmental stage through quantitative MS and PacBio sequencing (FIGS. 8A-8B and 9A-9F). Nuclear extracts were incubated with radiolabeled S-adenosyl-L-methionine (SAM) and PCR-amplified DNA substrate to assay for DNA methylase activity. Passage of the nuclear extract through an anion exchange column resulted in the elution of two distinct peaks of DNA methylase activity, both of which were heat sensitive (FIGS. 2C, 10A, and 10B). Western blot analysis confirmed that both peaks of activity mediate methylation on 6 mA (FIG. 10C). The resulting fractions were further purified and subjected to MS. Only four proteins-termed MTA1, MTA9, p1, and p2-were detected at higher abundance in fractions with high DNA methylase activity (FIGS. 2C and 2D). p1 and p2 contain homeobox-like domains, suggesting a DNA binding function for an undetermined process (FIG. 10D). On the other hand, MTA1 and MTA9 are both MT-A70 proteins. Such domains are widely known to mediate m6A RNA methylation in eukaryotes (Liu et al., 2014). MTA1 and MTA9 received the large majority of peptide matches, relative to all other MT-A70 genes encoded by the Tetrahymena genome (FIG. 2D; Table 6). Curiously, although poly(A)-selected RNA transcripts were present from all MT-A70 genes (FIG. 2D), almost all peptides in fractions with high DNA methylase activity corresponded to MTA1 and MTA9. The poly(A).sup.+ RNA expression profiles of MTA1, MTA9, p1, and p2 are remarkably similar (FIG. 9K), peaking early in the sexual cycle. This coincides with a sharp increase in nuclear 6 mA, as evidenced from immunostaining (Wang et al., 2017). Accumulation of MTA1, MTA9, p1, and p2 therefore correlates with the presence of 6 mA in vivo.

[0207] We next investigated the phylogenetic relationship of MTA1 and MTA9 to other eukaryotic MT-A70 domain-containing proteins. Two widely studied mammalian MT-A70 proteins—METTL3 and METTL14 (Ime4 and Kar4 in yeast)-form a heterodimeric complex that is responsible for m6A methylation on mRNA. METTL3 is the catalytically active subunit, while METTL14 functions as an RNA-binding scaffold protein (Sledi arid Jinek, 2016; Wang et al., 2016a, 2016b). MTA1 and MTA9 derive from distinct monophyletic clades, outside of those that contain mammalian METTL3, METTL14, and C. elegans DAMT-1 (METTL4) (FIG. 2A). Thus, MTA1 and MTA9 are divergent MT-A70 family members that are phylogenetically distinct from all previously studied RNA and DNA N6-methyladenine MTases. We then asked whether MTA1 and MTA9 are also present in other eukaryotes with a similar occurrence of 6 mA in ApT motifs as Tetrahymena. We queried the genomes of Oxytricha, green algae, and eight basal yeast species, all of which exhibit this distinct methylation pattern (as evidenced from FIGS. 1A-1E; FIGS. 9A-9E; Fu et al., 2015; Mondo et al., 2017). For all of these taxa, we can identify MT-A70 homologs that are monophyletic with MTA1 and MTA9 (FIG. 2B). On the other hand, MT-A70 homologs from multicellular eukaryotes, including Arabidopsis, C. elegans, Drosophila, and mammals, grouped exclusively with METTL3, METTL14, and METTL4 lineages, but not MTA1 or MTA9. None of these latter genomes exhibit a consensus ApT dinucleotide methylation motif for 6 mA (Greer et al., 2015; Koziol et al., 2016; Liang et al., 2018; Liu et al., 2016; Wu et al., 2016; Xiao et al., 2018; Zhang et al., 2015). We note that the absence of an ApT dinucleotide motif is based on data from a limited number of cell types, developmental stages, and culture conditions tested in these studies. Nonetheless, within the scope of currently available data, the presence of MTA1 and MTA9 correlates with the distinctive genomic localization of 6 mA within ApT motifs.

[0208] We then sought to determine whether MTA1 and/or MTA9 are bona fide 6 mA methyltransferases. MTA1, but not MTA9, contains a catalytic DPPW motif (FIG. 10E)—a hallmark of N6-adenosine methyltransferases (Iyer et al., 2016). Surprisingly, recombinant full-length Tetrahymena MTA1 and MTA9 (FIG. 10G) showed no detectable DNA methyltransferase activity, individually or together (FIG. 2E). Examination of the MTA1 and MTA9 sequences revealed that neither protein possesses a predicted nucleic acid binding domain (FIG. 10D). In contrast, METTL3, which catalyzes m6A methylation on RNA, contains two tandem CCCH-type zinc finger motifs, necessary for RNA binding (Huang et al., 2019; Wang et al., 2016a). Additional co-factors may thus be necessary for MTA1/7 to engage DNA substrates. Indeed, the p1 and p2 proteins that co-elute with MTA1/7 in nuclear extracts possess homeobox-like domains predicted to bind DNA. We then tested whether these accessory factors, in addition to MTA1/7, are necessary for 6 mA methylation. Strikingly, mixing recombinant, full-length p1, p2, MTA1, and MTA9 resulted in robust 6 mA methylation in vitro (FIGS. 2E and 2F). This activity was abolished when each protein was omitted, indicated that all four are necessary for 6 mA methylation. Furthermore, MTA1 harboring a D209A mutation in the catalytic DPPW motif showed no activity, even in the presence of MTA9, p1, and p2 (FIG. 2E). We also created double mutations in MTA1 (N370A, E371A), which lie in the conserved region that interacts with the 2′ and 3′-hydroxyl groups of the ribose moiety in the SAM cofactor (FIG. 2E). This mutant protein also exhibited no 6 mA methylase activity. Taken together, we find that four proteins—MTA1, MTA9, p1, and p2—are necessary for 6 mA methylation in vitro, with MTA1 the likely catalytic subunit. Henceforth, we refer to these four proteins as the putative MTA1 complex (MTA1c).

[0209] Purification of the MTA1c proteins from an E. coli overexpression system raises the possibility of methyltransferase activity arising from contaminating Dam methylase; however, we exclude this possibility for three reasons. (1) The DNA substrate used in this assay does not contain 5′-NATC-3′ sites, which are recognized and methylated by Dam methylase (Horton et al., 2006). (2) Methyltransferase activity was only observed when all four recombinant proteins were incubated with DNA. If contaminating Dam methylase were present in one or more of these protein preparations, then background activity should be observed when subsets of these proteins are used in the assay. 3) Mutation of MTA1 catalytic residues leads to loss of methylation, which is also inconsistent with contaminating methyltransferase activity.

TABLE-US-00006 TABLE 5 Candidate genes in ciliates. MT-A70 genes in Oxytricha trifallax Gene name in UniProt ID this study OxyDB gene name J9IF92_9SPIT MTA1 Contig12701.0.0.g16 J9IGS7_9SPIT TAMT-1 Contig17486.0.g100 J9J9V7_9SPIT MTA1-B Contig16314.0.g25 J9HW68_9SPIT MTA9 Contig1237.1.g126 J9IMU5_9SPIT MTA9-B Contig17413.0.g36 MT-A70 genes in Tetrahymena thermophila Gene name in Tetrahymena Genome UniProt ID this study Database gene name Q22GC0_TETTS MTA1 TTHERM_00704040 Q23TW8_TETTS MTA2 TTHERM_00962190 I7LVP8_TETTS MTA3/TAMT-1-B TTHERM_00136470 I7MGX6_TETTS MTA4 TTHERM_00558100 Q23RE0_TETTS MTA5/TAMT-1 TTHERM_00388490 I7MIF9_TETTS MTA9 TTHERM_00301770 Q22XT1_TETTS MTA9-B TTHERM_01005150 METTL16 homologs in Oxytricha trifallax UniProt ID OxyDB gene name J9F3J7_9SPIT Contig11945.0.g48 J9J5P9_9SPIT Contig7462.0.g41 J9III0_9SPIT Contig4244.0.g39 N6AMT1 homologs in Oxytricha trifallax UniProt ID OyDB gene name J9IFV1_9SPIT Contig7751.0.g12 Accessory factor genes in Tetrahymena thermophila Gene name in Tetrahymena Genome UniProt ID this study Database gene name Q22VV9_TETTS p1 TTHERM_00161750 I7M8B9_TETTS p2 TTHERM_00439330 ISWI homologs in Oxytricha trifallax and Tetrahymena thermophile Tetrahymena Genome UniProt ID OxyDB gene name Database gene name I7M280_TETTS TTHERM_00137610 J9FBJ2_9SPIT Contig11737.0.g12
The Uniprot ID of each gene is listed. The Oxytricha macronuclear genome encodes five genes belonging to the MT-A70 family (Iyer et al., 2016; Swart et al., 2013). Such genes commonly function as RNA m6 A MTases in eukaryotes, having evolved from m.MunI-like MTases in bacterial restriction-modification systems (Iyer et al., 2016). An MT-A70 gene belonging to the METTL4 subclade, DAMT1, is a putative 6 mA methyltransferase in C. elegans (Greer et al., 2015). However, none of the Oxytricha MT-A70 genes in this Table cluster together with METTL4 on a phylogenetic tree (FIGS. 2A and 9G). The Oxytricha genome also contains homologs of a structurally distinct RNA m6 A MTase, METTL16, which was reported to methylate U6 snRNA (Table 5) (Pendleton et al., 2017; Warda et al., 2017). Another candidate, N6AMT1—which does not contain an MT-A70 domain—was recently found to mediate DNA 6 mA methylation in human cells (Xiao et al., 2018). An N6AMT1 homolog is also present in the Oxytricha genome. Accessory factors refer to the p1 and p2 proteins, which are necessary for 6 mA methylation by MTA1 and MTA9 in vitro. The UniProt IDs of putative ISWI homologs in Oxytricha and Tetrahymena are also listed.

TABLE-US-00007 TABLE 6 Mass spectrometry analysis of MTA1, MTA9, p1, and p2 proteins. Data from Low Salt Fraction Gene name in % of protein covered by peptide UniProt ID this study data from LC-MS/MS experiment Q22GC0_TETTS MTA1 78.8% I7MIF9_TETTS MTA9 46.3% Q22W9_TETTS p1 41.9% I7M8B9_TETTS p2 81.7% Data from High Salt Fraction Gene name in % of protein covered by peptide UniProt ID this study data from LC-MS/MS experiment Q22GC0_TETTS MTA1 69.9% I7MIF9_TETTS MTA9 72.2% Q22VV9_TETTS p1 55.3% I7M8B9_TETTS p2 93.4%
Percentage of each polypeptide that is covered by peptide data is calculated. “Low Salt Sample” and “High Salt Sample” correspond to partially purified nuclear extracts that elute as two distinct peaks of activity from a Q sepharose anion exchange column (FIG. 2C).

Example 4

[0210] MTA1c Preferentially Methylates ApT Dinucleotides in dsDNA

[0211] We next investigated the substrate preferences of MTA1c. First, in vitro transcription was performed to generate doublestranded RNA (dsRNA) and single-stranded RNA (ssRNA) from the input dsDNA substrate. We found that MTA1c methylates dsDNA but not dsRNA or ssRNA of the same sequence, indicating that it is selective for DNA over RNA (FIG. 10H). We then generated a series of dsDNA substrates by annealing oligonucleotide pairs of different length and sequence. All of these substrates are bona fide Tetrahymena genomic DNA sequences. In each case, MTA1c can methylate the annealed dsDNA but not ssDNA (FIGS. 2G and 10I).

[0212] Since 6 mA methylation mainly lies in ApT dinucleotides in vivo (FIGS. 1D and 9D), we asked whether MTA1c preferentially methylates this motif. To test this, we used a 27 bp dsDNA substrate with two ApT dinucleotides in its native sequence (FIG. 2G). We disrupted one or both ApT motifs (FIG. 2G) by mutually swapping the 5′ A with a neighboring base 5′-CAT-3′.fwdarw.5′-ACT-3′. Disrupting both ApT dinucleotides resulted in >10-fold reduced methylation, while disrupting only one motif led to a 2- to 4-fold loss (FIGS. 2G and 10K).

[0213] Given that 6 mA occurs on both strands of genomic DNA in vivo (FIGS. 1E and 9E), we asked whether pre-existing methylation of one strand affects MTA1c activity. DNA oligonucleotides were nonspecifically methylated with 6 mA using EcoGII (Murray et al., 2018), a bacterial 6 mA methyltransferase. After rigorous purification, samples were annealed to an unmethylated, complementary strand to yield hemimethylated dsDNA (FIG. 10F). MTA1c activity was 3- to 3.5-fold higher on hemimethylated substrates, relative to unmethylated dsDNA (FIG. 2G). This effect was similar between dsDNA substrates pre-methylated on the sense or antisense strand, consistent with the lack of an overt strand bias in 6 mA locations in vivo (FIGS. 1E and 9E). Importantly, the increase in MTA1c activity cannot be attributed to contaminating EcoGII in hemimethylated substrates, since no activity was observed in the absence of MTA1c (FIG. 10J). Thus, pre-existing 6 mA methylation stimulates MTA1c, indicative of a positive feedback loop.

[0214] We then asked whether MTA1c activity is modulated not only by the dinucleotide motif sequence per se, but also by flanking sequences. This may manifest as the wide variation in frequency of DNA 4-mer containing a methylated ApT dinucleotide 5′-NA*TN-3′ in vivo (FIG. 10M). To test this, we used a dsDNA substrate containing two ApT dinucleotides, both within a 5′-CATT-3′. Swapping of the ApT motif with the adjacent downstream DNA residue produced substrates containing 5′-TATA-3′ (FIG. 10L). Substrates with this change at both locations had 4-fold less MTA1c activity, and an intermediate effect when only one dinucleotide was altered (FIG. 10L). These data indicate that 5′-CATT-3′ is the preferred methylation substrate, consistent with the higher frequency of methylated 5-CA*TT-3′ versus 5-TA*TA-3′ in both Tetrahymena and Oxytricha genomic DNA (FIG. 10M). The difference in frequency of methylated sequences cannot simply be attributed to the higher frequency of the 4nt 5′-CATT-3′ motif versus 5′-TATA-3′ in the genome, because the opposite trend is observed (FIG. 10N). Thus, MTA1c is sensitive to variation in DNA sequences flanking the ApT dinucleotide motif.

Example 5

MTA1 is Necessary for 6 mA Methylation In Vivo

[0215] Having established that MTA1c is a 6 mA methyltransferase, we tested the role of MTA1c in mediating 6 mA methylation in vivo in Oxytricha, for which we have ease of generating mutants. The genome-wide localization of 6 mA is conserved between Oxytricha and Tetrahymena (FIGS. 1A-1E and 9A-9F), implying similar underlying enzymatic machinery. Indeed, all four component genes—MTA1, MTA9, p1, and p2—are clearly conserved between both species (FIGS. 9G-9J). The DPPW catalytic motif is also completely conserved in Tetrahymena and Oxytricha MTA1 but not MTA9, suggesting that MTA1 is the likely catalytic subunit of MTA1c in both ciliates (FIG. 10E). To abrogate MTA1c function, we disrupted the Oxytricha MTA1 gene by inserting an ectopic DNA sequence 49 bp downstream of the start codon, resulting in a frameshift mutation and loss of the C-terminal MTase domain (FIG. 3A). Oxytricha has two MTA1 paralogs, named MTA1 and MTA1-B (FIGS. 2A and 9G). We focused on MTA1 because MTA1-B is not expressed in vegetative Oxytricha cells (Swart et al., 2013), which we used to profile 6 mA locations via SMRT-seq. Dot blot analysis confirmed a significant reduction in bulk 6 mA levels in mutant lines (FIG. 3B). We then examined 6 mA positions at high resolution using SMRT-seq to understand how the DNA methylation landscape is altered in mta1 mutants. Notably, these mutants exhibit genome-wide loss of 6 mA, with complete abolishment of the dimethylated ApT motif, and reduction in frequency of all other methylated dinucleotide motifs (FIGS. 3C-3E). These findings are consistent across all biological replicates and are robust to wide variation in SMRT-seq parameters for calling 6 mA modifications (FIGS. 11B-11D). It cannot be attributed to variation in sequencing coverage between wild-type and mutant lines. The loss of methylated ApT dinucleotides in mta1 mutants is consistent with our in vitro data suggesting that MTA1c primarily methylates ApT sites (FIGS. 2G and 10K). The Inter Pulse Duration ratio (degree of polymerase slowing during PacBio sequencing due to presence of a modified base) and estimated fractional methylation also decreased significantly at called 6 mA sites in mta1 mutants (p<2.2×10-16, Wilcoxon rank-sum test) (FIG. 11A). MTA1 is therefore necessary for a significant proportion of in vivo 6 mA methylation events in Oxytricha.

[0216] What are the phenotypic consequences of 6 mA loss in vivo? It has been proposed that DNA methylation—including 6 mA and cytosine methylation—is involved in nucleosome organization (Fu et al., 2015; Huff and Zilberman, 2014). We thus asked whether nucleosome organization is altered in mta1 mutants. We quantified nucleosome “fuzziness,” defined as the SD of MNase-seq read locations surrounding the called nucleosome peak (Lai and Pugh, 2017; Mavrich et al., 2008). A poorly positioned nucleosome consists of a shallow and wide peak of MNase-seq reads, manifested by a high fuzziness score. Nucleosomes were first grouped according to the change in flanking 6 mA between wild-type and mta1 mutant cells (FIGS. 12A-12G). The nucleosomes that experience large changes in flanking 6 mA exhibit significantly greater increase in fuzziness, compared to nucleosomes with little change in flanking 6 mA (FIGS. 12A and 12D). Such nucleosomes also exhibit changes in occupancy that are consistent with an increase in fuzziness (FIGS. 12A and 12E). These results are robust to variation in MNase digestion (FIGS. 14C and 14D). On the other hand, nucleosome linkers do not change in length or occupancy, even though 6 mA is lost from these regions (FIGS. 12B, 12C, 12F, and 12G). We conclude that 6 mA exerts subtle effects on nucleosome organization in vivo.

Example 6

6 mA Disfavors Nucleosome Occupancy Across the Genome In Vitro but not in Vivo

[0217] Multiple factors, including 6 mA, DNA sequence, and chromatin remodeling complexes, may collectively contribute to nucleosome organization in vivo. The effect of 6 mA could therefore be masked by these elements. We next sought to determine whether 6 mA directly impacts nucleosome organization. To this end, we assembled chromatin in vitro using Oxytricha gDNA, which contains cognate 6 mA. To obtain a matched negative control lacking DNA methylation, 98 complete chromosomes were amplified using PCR (FIG. 4A), purified and subsequently mixed together in stoichiometric ratios to obtain a “mini-genome” (FIG. 4B). These chromosomes collectively reflect overall genome properties, including AT content, chromosome length, and transcriptional activity (Table 7). Native genomic DNA (containing 6 mA) and amplified mini-genome DNA (lacking 6 mA) were each assembled into chromatin in vitro using Xenopus or Oxytricha histone octamers (FIGS. 13A-13F) and analyzed using MNase-seq. We computed nucleosome occupancy from the native genome and mini-genome samples across 199,795 overlapping DNA windows, spanning all base pairs in the 98 chromosomes. This allowed the direct comparison of nucleosome occupancy in each window of identical DNA sequence, with and without 6 mA (FIGS. 4C and 4D). Windows exhibit lower nucleosome occupancy with increasing 6 mA, confirming the quantitative nature of this effect. Furthermore, similar trends were observed for both native Oxytricha and recombinant Xenopus histones, suggesting that the effects of 6 mA on nucleosome organization arise mainly from intrinsic features of the histone octamer rather than from species-specific variants (FIGS. 4C and 4D). These results are also robust to the extent of MNase digestion of reconstituted chromatin (FIG. 14A).

[0218] We then directly compared the impact of 6 mA on nucleosome occupancy in vitro and in vivo. Loss of 6 mA in vitro is achieved by mini-genome construction, while loss in vivo is achieved by the mta1 mutation. For each overlapping DNA window, we calculated the difference in nucleosome occupancy: (1) between native genome and mini-genome DNA in vitro, and (2) between wild-type and mta1 mutants in vivo (FIG. 4C). Nucleosome occupancy is indeed lower in the presence of 6 mA methylation in vitro (FIGS. 4C and 4D). In contrast, no change in nucleosome occupancy is observed in vivo (FIGS. 4C and 4E). This result is consistent with our earlier analysis of linker occupancy in mta1 mutants (FIGS. 12C and 12G). We note that highly methylated DNA windows show greater change in 6 mA relative to mta1 mutants (FIG. 3D). Yet, these windows do not change in nucleosome occupancy in vivo. We conclude that 6 mA methylation locally disfavors nucleosome occupancy in vitro, but that this intrinsic effect can be overcome by endogenous chromatin factors in vivo.

TABLE-US-00008 TABLE 7 Descriptive statistics of reference genomes. Native genomic DNA Mini-genome DNA Chromosome 2449 +/− 742 2107 +/− 778  length (bp) Min = 1155 Min = 1201 Max = 6494 Max = 4659 SMRT-seq  177.4 +/− 117.0 205.3 +/− 136.1 coverage (x) Min = 75.1 Min = 77.8 Max = 1392.6 Max = 918.4 Total number 46,322 2,344 of 6mA marks in genome 6mA sites per 12 +/− 8 24 +/− 16 chromosome Min = 0 Min = 0 Max = 73 Max = 73 AT content (%) 67.8 +/− 3.0 66.5 +/− 2.7  Min = 55.7 Min = 60.2 Max = 76.2 Max = 72.2 RNAseq  34.4 +/− 75.2 53.7 +/− 71.5 (FPKM) Min = 0.0 Min = 0.1 Max = 1444.5 Max = 424.8
Properties of Oxytricha chromosomes in native genomic DNA and mini-genome DNA. “+/−” indicates one standard deviation above or below the mean.

Example 7

Modular Synthesis of Epigenetically Defined Chromosomes

[0219] The above experiments used kinetic signatures from SMRT-seq data to infer the presence of 6 mA marks in genomic DNA. We next sought to confirm that 6 mA is directly responsible for disfavoring nucleosomes in vitro, and to understand how this effect could be overcome by cellular factors. 6 mA-containing oligonucleotides were annealed and subsequently ligated with DNA building blocks to form full-length chromosomes. Importantly, these chromosomes contain 6 mA at all locations identified by SMRT-seq in vivo. The representative chromosome, Contig1781.0, is 1.3 kb, contains a clearly defined TSS, and encodes a single highly transcribed gene with a predicted RING finger domain. The length and gene structure are characteristic of typical Oxytricha chromosomes (FIG. 5A). We independently validated the location of 6 mA in vivo by sequencing chromosomal DNA immunoprecipitated with an anti-6 mA antibody (FIG. 5A).

[0220] Four chromosome variants were synthesized, with cognate 6 mA sites on neither, one, or both DNA strands (chromosomes 1-4 in FIGS. 5B and 5C). Chromatin was assembled by salt dialysis with either Oxytricha or Xenopus nucleosomes and subsequently digested with MNase to obtain mononucleosomal DNA (FIGS. 6A and 13G). Tiling qPCR was used to quantify nucleosome occupancy at ˜50 bp increments along the entire length of the synthetic chromosome (FIG. 6B). The fully methylated locus exhibits a ˜46% reduction in nucleosome occupancy relative to the unmethylated variant, while hemimethylated chromosomes containing half the number of 6 mA marks showed intermediate nucleosome occupancy at the corresponding region (FIG. 6B). The reduction in nucleosome occupancy was confined to the methylated region and not observed across the rest of the chromosome. Similar trends were observed when chromatin was assembled using the NAP1 histone chaperone (FIG. 14F. top panel). indicating that this effect is not an artifact of the salt dialysis method. Furthermore, moving 6 mA to an ectopic location (chromosome 5 in FIGS. 5B and 5C) decreases nucleosome occupancy at that site (FIG. 6C). We conclude that 6 mA directly disfavors nucleosome occupancy in a local, quantitative manner in vitro.

Example 8

Chromatin Remodelers Restore Nucleosome Occupancy Over 6 mA Sites

[0221] Nucleosome occupancy in vivo is influenced not only by DNA sequences but also by trans-acting factors such as ATP-dependent chromatin remodeling factors (Struhl and Segal, 2013). We used synthetic, methylated chromosomes to test how the well-studied chromatin remodeler ACF responds to 6 mA in native DNA. ACF generates regularly spaced nucleosome arrays in vitro and in vivo (Clapier and Cairns, 2009; Ito et al., 1997). Its catalytic subunit ISWI is conserved across eukaryotes, including Oxytricha and Tetrahymena (Table 5). Synthetic chromosomes were assembled into chromatin by salt dialysis as before and then incubated with ACF in the presence of ATP (FIGS. 13H and 6D). We find that ACF partially—but not completely—restores nucleosome occupancy over the methylated locus in an ATP-dependent manner (FIG. 6D). This effect is observed when ACF was added to chromatin assembled by salt dialysis or the NAP1 histone chaperone (FIGS. 6D and 14F). ACF also restores nucleosome occupancy over methylated loci in native genomic DNA (FIGS. 6E and 13I), indicating that the effect is not restricted to a single chromosome. This result is robust to the extent of MNase digestion (FIG. 14B). Although the heterologous system used here may differ from endogenous chromatin assembly factors in Oxytricha, our experiment illustrates the principle that trans-acting factors can counteract or even overcome the effect of 6 mA on nucleosome organization.

Example 9

Disruption of MTA1 Impacts Gene Expression and Sexual Development

[0222] Since mta1 mutants exhibit genome-wide loss of 6 mA, we assayed these cells for transcriptional changes by poly(A).sup.+ RNAseq. Only a small minority of genes show significant changes in gene expression (10% false discovery rate [FDR]; FIG. 7A). To examine the methylation status of these differentially expressed genes, we grouped them according to “starting” methylation level, as defined by the total number of 6 mA marks near the TSS in wild-type cells. Genes exhibit two distinct transcriptional responses: those with low starting levels of 6 mA exhibit a small change in 6 mA between wild-type and mutant cells (FIG. 3D) and tend to be significantly upregulated in mutant lines (p=2.8×10.sup.−9, Fisher's exact test; FIG. 7B). Surprisingly, genes with high starting 6 mA are not enriched in differentially expressed genes (p>0.1, Fisher's exact test), even though they exhibit greater loss of 6 mA in mutants (FIG. 3D). Steady-state RNA-seq levels are therefore largely robust to drastic changes in 6 mA levels. Since most, but not all, 6 mA is lost from mta1 mutants (FIG. 3C), it is also possible that residual DNA methylation across the genome sufficiently buffers genes from changes in transcription.

[0223] Because the aforementioned phenotypic changes were assayed in vegetative Oxytricha cells, we asked whether MTA1 may play roles outside of this developmental state. MTA1 transcript levels are markedly upregulated in the sexual cycle, as assayed by poly(A). RNA-seq (FIG. 7C). Strikingly, mta1 mutants fail to complete the sexual cycle when induced to mate and display complete lethality (FIG. 7D). Our data do not exclude the possibility that m6A RNA methylation, in addition to 6 mA DNA methylation, is also impacted by MTA1 loss during development. Further studies would clarify the role of MTA1 in these pathways.

Example 10

Discussion

[0224] The present disclosure has identified MTA1c as a conserved, hitherto undescribed 6 mA methyltransferase. It consists of two MT-A70 proteins (MTA1/MTA9) and two homeobox-like proteins (p1/p2). The composition of MTA1c provides immediate insights into how it specifically methylates DNA (FIG. 7F). MTA1 likely mediates transfer of the methyl group from SAM to the acceptor adenine moiety, given that it contains conserved amino acid residues implicated in catalysis and SAM binding (FIG. 10E). Indeed, we show that these residues are necessary for its activity (FIG. 2E). While MTA1 constitutes the catalytic center, it lacks a CCCH-type zinc finger domain that is necessary for RNA binding in the canonical m6A methyltransferase METTL3. Instead, nucleic acid binding is likely assumed by the homeobox-like domains in p1 and p2, which are known to specifically engage dsDNA through helix-turn-helix motifs.

[0225] The observation that MTA1c is more active in the presence of pre-methylated DNA templates is reminiscent of the CpG methyltransferase DNMT1. Yet, MTA1c and DNMT1 exhibit distinct protein domain architectures. Further biochemical studies are required to elucidate the molecular basis of this property. A distinct MT-A70 protein, named TAMT-1, was recently reported to act as a 6 mA methyltransferase in Tetrahymena, (Luo et al., 2018), suggesting that multiple enzymes mediate 6 mA deposition. It remains to be determined how MTA1c and TAMT-1 collectively mediate DNA methylation at various developmental stages, and whether cross-talk occurs between these enzymes.

[0226] In addition to identifying the ciliate 6 mA methyltransferase, we investigated the function of 6 mA in vitro by building epigenetically defined chromosomes. We show that 6 mA directly disfavors nucleosome occupancy in a local, quantitative manner, independent of DNA sequence (FIG. 7E). Our experiments do not reveal exactly how 6 mA disfavors nucleosome occupancy. Early studies suggest that 6 mA destabilizes dA:dT base pairing, leading to a decrease in the melting temperature of DNA (Engel and von Hippel, 1978). Whether this or some other property of 6 mA contributes to lowered nucleosome stability awaits further investigation.

[0227] Intriguingly, nucleosome organization exhibits only subtle changes after genome-wide loss of 6 mA (FIG. 7E). Only a small set of genes (<10%) is transcriptionally dysregulated. It is possible that residual 6 mA in mta1 mutants could mask relevant phenotypes. Nonetheless, our results caution against interpreting 6 mA function solely based on correlation with genomic elements. We also find that 6 mA intrinsically disfavors nucleosomes in vitro, but—crucially—this effect can be overridden by distinct factors in vitro and in vivo. We propose that phased nucleosome arrays are first established in vivo, which then restrict MTA1-mediated methylation to linker regions due to steric hindrance. This in turn decreases the fuzziness of flanking nucleosomes, reinforcing chromatin organization. Therefore, 6 mA tunes nucleosome organization in vivo. Our data do not support the hypothesis that nucleosome phasing is established by predeposited 6 mA.

[0228] More broadly, our work showcases the utility of Oxytricha chromosomes for advancing chromatin biology. By extending current technologies (Muller et al., 2016), it should be feasible to introduce both modified nucleosomes and DNA methylation in a site-specific manner on full-length chromosomes. Such “designer” chromosomes will serve as powerful tools for studying DNA-templated processes such as transcription within a fully native DNA environment.

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[0327] The embodiments described in this disclosure can be combined in various ways. Any aspect or feature that is described for one embodiment can be incorporated into any other embodiment mentioned in this disclosure. While various novel features of the inventive principles have been shown, described and pointed out as applied to particular embodiments thereof, it should be understood that various omissions and substitutions and changes may be made by those skilled in the art without departing from the spirit of this disclosure. Those skilled in the art will appreciate that the inventive principles can be practiced in other than the described embodiments, which are presented for purposes of illustration and not limitation.