Compositions and methods for down-regulating genes through oral administration of RNAi molecule encapsulated in plant cells are provided.

Anti-sense-oriented RNA gene suppression agents in the form of a loop of anti-sense-oriented RNA is produced in cells of transgenic organisms, e.g. plants, by transcription from a recombinant DNA construct that comprises in 5′ to 3′ order a promoter element operably linked to more than one anti-sense-oriented DNA element and one or more complementary DNA elements.

The present invention relates to methods of synthesizing long-chain polyunsaturated fatty acids, especially eicosapentaenoic acid, docosapentaenoic acid and docosahexaenoic acid, in recombinant cells such as yeast or plant cells. Also provided are recombinant cells or plants which produce long-chain polyunsaturated fatty acids. Furthermore, the present invention relates to a group of new enzymes which possess desaturase or elongase activity that can be used in methods of synthesizing long-chain polyunsaturated fatty acids. In particular, the present invention provides ω3 destaurases, Δ5 elongases and Δ6 desaturases with novel activities. Also provided are methods and DNA constructs for transiently and/or stably transforming cells, particularly plant cells, with multiple genes.

Transgenic plants that have enhanced yield-related traits, such as increased seed oil production, are produced by genetically engineering the plants to down-regulate the expression of at least one BPM protein. Such transgenic plants can, for example, be cultivated and yield higher seed oil production than control plants which have not been genetically engineered for down regulation of a BPM protein.

The present invention provides a new plant gene-rice high temperature resistance 1 gene (Rice High Temperature Resistance 1, HTR1) and encoded protein thereof. Also disclosed is the use of the high temperature resistance gene, especially for the enhancement of high-temperature resistance of plants in plant variety improvement and cross breeding.

A gene LBA5 for regulating lateral shoot angles, growth habits, and a plant architecture of Arachis hypogaea L., and use thereof are provided. In the present disclosure, a major gene LBA5 for controlling lateral shoot angles, growth habits, and a plant architecture of Arachis hypogaea L. is mapped and cloned from Arachis hypogaea L., which includes two homologous genes LBA5b and LBA5a and promoters thereof. The allelic variations of the gene can be selected through crossbreeding and backcrossing to achieve the genetic improvement on an angle between an Arachis hypogaea L. lateral shoot and a main stem. Through a genetic engineering operation for the gene and a change for a promoter sequence of the gene, the function or expression level of this gene in a procumbent Arachis hypogaea L. variety can be adjusted to further regulate an angle between an Arachis hypogaea L. lateral shoot and a main stem.

The present disclosure provides methods for increasing meiotic recombination in crop plants, as well as plants and seeds produced by such methods.

The invention provides corn event MON 87411, and plants, plant cells, seeds, plant parts, and commodity products comprising event MON 87411. The invention also provides polynucleotides specific for event MON 87411 and plants, plant cells, seeds, plant parts, and commodity products comprising polynucleotides specific for event MON 87411. The invention also provides methods related to event MON 87411.

Provided herein is a method for improving growth, stress tolerance and productivity of a plant. Also provided herein is a method for increasing seed quality of a plant. Specifically, the disclosure provides a method for improving growth, stress tolerance and productivity of a plant, comprising: providing a transgenic plant, which includes a reduced expression on an MYBS2 gene as relative to its wild-type counterpart; and a method for increasing seed quality of a plant, comprising: providing a seed from a transgenic plant, which overexpresses a full-length MYBS2 gene or a mutant MYBS2 gene as relative to its wild-type counterpart.

A CC-NBS-LRR gene NLR1-V encoded by the enduring and broad-spectrum gene Pm21 which is resistant to powdery mildew in the wheat-Haynaldia villosa 6VS/6AL translocation line in Nannong 9918, and an expression vector and use thereof. The ORF sequence of the NLR1-V gene having an NLR domain is as shown in SEQ ID NO: 1, and the encoded amino acid sequence is as shown in SEQ ID NO: 2.