Method of Increasing the Effective Tiller Number of Rice Plant

Abstract

Provided is a method of increasing the effective tiller number of a rice plant, including overexpressing a gene having a nucleic acid sequence as shown in SEQ ID NO: 1 in the rice plant. The gene encodes a protein which interacts with MOC1 in the rice plant.

Claims

1. A method of increasing the effective tiller number of a rice plant, comprising overexpressing a gene having a nucleic acid sequence as shown in SEQ ID NO: 1 in the rice plant.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0015] The specific embodiments of this invention are described in detail with the accompanying drawings.

[0016] FIG. 1 shows the expression level of gene LOC_OS05G38680 in the rice transgenic lines.

[0017] FIG. 2 shows plant phenotypes of the rice transgenic lines overexpressing gene LOC_OS05G38680.

[0018] FIG. 3 shows statistics of the effective tiller number of the rice transgenic lines overexpressing gene LOC_OS05G38680.

[0019] For all figures, WT refers to the wild-type control variety Nipponbare; OE1 and OE2 refer to the two different rice transgenic lines overexpressing gene LOC_OS05G38680. ‘*’ and ‘**’ indicate the significance (P<0.05) and the extreme significance (P<0.01) by t-test between the transgenic line and the wild-type control.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0020] Step 1. Extraction of Total RNA from Rice and Synthesis of cDNA

[0021] Rice total RNA was extracted from the leaves of the wild-type variety Nipponbare by RNeasy Plant Mini Kit (QIAGEN, Germany) according to the product's instructions, and was reversely transcribed into the cDNA by PrimeScript™ 1st Strand cDNA Synthesis Kit (TaKaRa, Japan) according to the product's instructions.

[0022] Step 2. PCR Amplification of Gene LOC_Os05g38680

[0023] PCR amplification of gene LOC_Os05g38680 was carried by PrimeSTAR® HS DNA Polymerase (TaKaRa, Japan). The sequences of the primers are F1: 5′-CGGGGTACCAGATAGATAAGTAAGCAGTGAG-3′ (SEQ ID NO: 2) and R1: 5′-AAAACTGCAGGATGCATGCTTACGGCACAT-3′ (SEQ ID NO: 3). The reaction solution of PCR was prepared according to the product's instructions, and PCR process were used as: 5 min at 95° C.; 10 sec at 98° C. for denaturation, 15 sec at 55° C. for annealing, 30 sec at 72° C. for extension, 30 cycles; and 5 min at 72° C.

[0024] Step 3. Enzymes Digestion and Purification of the PCR Products

[0025] The PCR products of gene LOC_Os05g38680 were purified bye the AxyPrep PCR cleaning kit (Axygen, USA) according to the product's instructions. Then, the purified products were digested by two restriction enzymes, Kpn I and Pst I (TaKaRa, Japan), and the digestion system included 1 μL Kpn I, 1 μL Pst I, 3 μl Buffer M (TaKaRa company restriction enzyme Buffer M), 10 μL PCR product, ddH.sub.2O to make up to 20 μL, and then was incubated at 37° C. for 4 h. Finally, the digestion products were purified by the AxyPrep PCR cleaning kit (Axygen, USA) again.

[0026] Step 4. Enzymes digestion and purification of pCAMBIA1300-2×35S vector

[0027] The plasmid of vector pCAMBIA1300-2×35S was digested and purified according to the method in Step 3.

[0028] Step 5. Overexpression Vector Construction of Gene LOC_Os05g38680

[0029] {circle around (1)} The purified products obtained in Step 3 and Step 4 were ligated by the T4 ligase Kit (Promega, USA). The ligation system included 1 μL digested plasmid of the pCAMBIA1300-2×35S vector, 2 μL digested PCR fragment of gene LOC_Os05g38680, 0.5 μL T4 ligase, 1 μL ligation Buffer, ddH.sub.2O supplement to 10 μL, and then was incubated overnight (12 h) at 4° C.

[0030] {circle around (2)} Ten μL ligation products obtained from step {circle around (1)} were mixed with the bacterial competent cells of JM109 and incubated for 30 min in ice bath; then the bacterial mixture was incubated in water bath at 42° C. for 90s and immediately transferred on ice for 10 min; 800 μL LB medium without any antibiotics was added into the bacterial mixture and incubated at 37° C. for 1 h on the shaker; finally, the bacterial mixture was spread on the LB medium plate containing Kanamycin (25 mg/L) and incubated at 37° C. overnight.

[0031] {circle around (3)} Monoclonal colonies on the plate were separately picked into test tubes with 4 mL of LB medium (Kanamycin 25 mg/L), and incubated overnight at 37° C. with a rotational speed 200 r/min on the shaker. the bacterial fluid of each tubes was identified by PCR using the 2×Taq PCR premix reagent (Tiangen, Beijing). PCR reaction system included 1 μL bacteria fluid, 10 μL 2×Taq PCR MasterMix II, 1 μL F1+R1 primers (10 μM), ddH.sub.2O up to 20 μL. The PCR process were used as: 5 min at 94° C.; 30 sec at 94° C. for denaturation, 30 sec at 55° C. for annealing, 30 sec at 72° C. for extension, 35 cycles; and 5 min at 72° C. Then, 5 μL PCR products of each reaction was detected by agarose-gel electrophoresis.

[0032] {circle around (4)} The positive colonies identified by PCR were sent to the biotechnology company for sequencing the sequence of gene LOC_OS05g38680 inserted into the vector pCAMBIA-1300. The universal primers P1: 5′-CCAGGCTTTACACTTTATGC-3′ (SEQ ID NO: 4) and P2: 5′-GCGATTAAGTTGGGTAACGC-3′ (SEQ ID NO: 5) were used for sequencing. The vector containing a correct sequence of gene LOC_OS05G38680 was used for further rice transformation. The nucleotide sequence of gene LOC_Os05g38680 in the vector was shown in SEQ ID NO: 1.

[0033] Step 6. Genetic Transformation of Rice

[0034] The vector constructed from Step 5 was transformed into a wild-type rice variety Nipponbare using the method of Nishimura et al. (Nishimura et al, Nat Protoc, 2006) to obtain the transgenic rice plants.

[0035] Step 7. Identification of the Transgenic Plants

[0036] The extraction of the total RNAs from the transgenic plants and cDNA synthesis were followed by the methods described in Step 1. The expression levels of gene LOC_Os05g38680 in the transgenic plants were analyzed by Real-time PCR using the primer pair F2: 5′-GGAGCTTGCTGATCCAGTAGTC-3′ (SEQ ID NO: 6) and R2: 5′-TAGCTAGAGCTCATGTGAAGAG-3′ (SEQ ID NO: 7). The SYBR® Premix Ex Taq™ II Kit (TakaRa, Japan) was used for Real-time PCR, and the reaction system included 10 μL SYBR® Premix Ex Taq® II, 2 μL cDNA template, 1 μL F2+R2 primers (10 μM each), 0.4 μL ROX Reference Dye, ddH.sub.2O up to 20 μL. Rice housekeeping gene Actin was used for the standard normalization, the PCR primers are F3: 5′-TGGCATCTCTCAGCACATTCC-3′ (SEQ ID NO: 8) and R3: 5′-TGCACAATGGATGGGTCAGA-3′ (SEQ ID NO: 9). PCR process was performed as: 95° C. for 30s; 95° C. for 5s and 60° C. for 30s, 40 cycles. Three replicates were done for each sample, and the data were analyzed using the 2.sup.−ΔΔCT method (Livak KJ and Schmittgen TD, Methods, 2001), and the significances between the transgenic plants and the wild-type control were analyzed by the t-test method.

[0037] As the results of Real-time PCR, the two transgenic lines (OE1 and OE2) were identified with high expression levels of gene LOC_Os05g38680, which were significantly higher than that in the wild-type control (FIG. 1)

[0038] Step 8. Statistical Investigation of Effective Tillers Number in the Transgenic Lines

[0039] In May, rice seeds were sowed in south China, and transplanted in fields at June in the same year. After maturity (October in the same year), each 20 plants were randomly selected from the two transgenic lines (OE1 and OE2) and the wild-type control Nipponbare for investigating the number of effective tillers per plant. The significances between the two transgenic lines and the wild-type control were analyzed by the t-test.

[0040] As a result of the statistical investigation, the number of effective tillers per plant both in the two transgenic lines (OE1 and OE2) were significantly higher than that in the wild-type control (FIG. 2 and FIG. 3), indicating that enhancing the expression level of gene LOC_Os05g38680 could effectively increase the number of effective tillers in rice.

[0041] Finally, it is important to note that the above lists are only specific embodiments of the present invention. Obviously, the invention is not limited to the above embodiments, but can also have a lot of deformation. All the deformation that the general technical personnel in this field can directly derive or associate with the contents disclosed in this field should be considered as the scope of protection of the invention.