This invention is directed to methods of switching from sexual reproduction to apomixis or from apomixis to sexual reproduction in a eukaryote. More particularly, this invention provides methods of switching from meiosis to apomeiosis and from syngamy to parthenogenesis in a plant. The invention also provides methods of producing an apomictic eukaryote from a sexual eukaryote and a sexual eukaryote from an apomictic eukaryote.

The present invention refers to methods for selectively recognizing a base pair in a DNA sequence by a polypeptide, to modified polypeptides which specifically recognize one or more base pairs in a DNA sequence and, to DNA which is modified so that it can be specifically recognized by a polypeptide and to uses of the polypeptide and DNA in specific DNA targeting as well as to methods of modulating expression of target genes in a cell.

This document relates to methods and materials for genome engineering in eukaryotic cells, and particularly to methods for increasing genome engineering (i.e. transformation or genome editing) efficiency via delivery of one or more RKD2 and RKD4 genes, with genome engineering components.

The present invention relates to an expression control element and expression system comprising same, particularly to an expression control element regulated by a polyamine or polyamine analogue, host cells and eukaryotic organisms comprising same and methods of use thereof.

The present invention provides the specific expression promoters in rice and the application. The present invention applies the promoter in the plant genetic engineering. The sequence of the promoter provided in the present invention is composed of the nucleotide sequence shown in SEQ ID No. 1; the nucleotide sequence shown in SEQ ID No. 2; Or the nucleotide sequence shown in SEQ ID No. 3.

The present invention refers to methods for selectively recognizing a base pair in a DNA sequence by a polypeptide, to modified polypeptides which specifically recognize one or more base pairs in a DNA sequence and, to DNA which is modified so that it can be specifically recognized by a polypeptide and to uses of the polypeptide and DNA in specific DNA targeting as well as to methods of modulating expression of target genes in a cell.

The invention provides a genetically modified plant or plant cell transformed with an isolated nucleic acid, wherein the isolated nucleic acid encodes a SYAC1 protein or a protein related to the SYAC1 protein or a protein with at least about 80%, 85%, 90%, 95%, 98%, 99% or more sequence identity protein with a SYAC1 protein. The invention also provides a genetically modified plant or plant cell engineered to express a reduced level, or no, SYAC1 protein. A genetically modified plant according to the invention may be more resistant to infection by Plasmodiophora brassicae. Alternatively, the invention provides a genetically modified plant with increased levels of SYAC1 protein or related protein which is more receptive to beneficial microorganisms and/or grows more effectively on land contaminated with heavy metals.

This document relates to methods and materials for genome engineering in eukaryotic cells, and particularly to methods for increasing genome engineering (i.e. transformation or genome editing) efficiency via co-delivery of one or more chemicals, such as protein deacetylase inhibitors, phytohormones and/or regeneration boost genes, with genome engineering components.

This invention provides molecular constructs and methods for the temporally specific control of gene expression in plants or in plant pests or pathogens. More specifically, this invention provides plant miRNA genes having novel circadian expression patterns that are useful for designing recombinant DNA constructs for temporally specific expression of at least one gene. Also provided are non-natural transgenic plant cells, plants, and seeds containing in their genome a recombinant DNA construct of this invention.

This invention provides a drug-inducible promoter that can be used for sugarcane plants and plants related thereto. Such drug-inducible promoter comprises a polynucleotide comprising a first nucleotide sequence having 90% or higher identity to the nucleotide sequence as shown in SEQ ID NO: 1, a second nucleotide sequence having 90% or higher identity to the nucleotide sequence as shown in SEQ NO: 2, a third nucleotide sequence having 90% or higher identity to the nucleotide sequence as shown in SEQ ID NO: 3, a fourth nucleotide sequence having 90% or higher identity to the nucleotide sequence as shown in SEQ ID NO: 4, and a fifth nucleotide sequence having 90% or higher identity to the nucleotide sequence as shown in SEQ ID NO: 5 in such an order from the 3 terminal side toward the 5′ terminal side.