A soybean cultivar designated S140159 is disclosed. The invention relates to the seeds of soybean cultivar S140159, to the plants of soybean cultivar S140159, to the plant parts of soybean cultivar S140159, and to methods for producing progeny of soybean cultivar S140159. The invention also relates to methods for producing a soybean plant containing in its genetic material one or more transgenes and to the transgenic soybean plants and plant parts produced by those methods. The invention also relates to soybean cultivars or breeding cultivars, and plant parts derived from soybean cultivar S140159. The invention also relates to methods for producing other soybean cultivars, lines, or plant parts derived from soybean cultivar S140159, and to the soybean plants, varieties, and their parts derived from use of those methods. The invention further relates to hybrid soybean seeds, plants, and plant parts produced by crossing cultivar S140159 with another soybean cultivar.

A soybean cultivar designated S140159 is disclosed. The invention relates to the seeds of soybean cultivar S140159, to the plants of soybean cultivar S140159, to the plant parts of soybean cultivar S140159, and to methods for producing progeny of soybean cultivar S140159. The invention also relates to methods for producing a soybean plant containing in its genetic material one or more transgenes and to the transgenic soybean plants and plant parts produced by those methods. The invention also relates to soybean cultivars or breeding cultivars, and plant parts derived from soybean cultivar S140159. The invention also relates to methods for producing other soybean cultivars, lines, or plant parts derived from soybean cultivar S140159, and to the soybean plants, varieties, and their parts derived from use of those methods. The invention further relates to hybrid soybean seeds, plants, and plant parts produced by crossing cultivar S140159 with another soybean cultivar.

A method of modifying the genome of an organism, wherein the modification method includes modifying the genome of the organism by using in a cell of the organism a protein having an optimal temperature for double-stranded DNA breakage activity in an ordinary temperature region.

A New Guinea Impatiens plant designated SAKIMP044 is disclosed. Embodiments include seeds of New Guinea Impatiens SAKIMP044, plants of New Guinea Impatiens SAKIMP044, to plant parts of New Guinea Impatiens SAKIMP044, and methods for producing an impatiens plant produced by crossing New Guinea Impatiens SAKIMP044 with itself or with another impatiens variety. Embodiments include methods for producing an impatiens plant containing in its genetic material one or more genes or transgenes and transgenic impatiens plants and plant parts produced by those methods. Embodiments also relate to impatiens varieties, breeding varieties, plant parts, and cells derived from New Guinea Impatiens SAKIMP044, methods for producing other impatiens lines or plant parts derived from New Guinea Impatiens SAKIMP044, and the impatiens plants, varieties, and their parts derived from use of those methods. Embodiments further include hybrid impatiens seeds, plants, and plant parts produced by crossing New Guinea Impatiens SAKIMP044 with another impatiens variety.

The present invention relates to a Lactuca sativa seed designated 81-01 RZ, which exhibits a combination of traits including resistance to downy mildew (Bremia lactucae) races B1:1 to B1:28, B1:30 to B1:32 and Ca-I to Ca-VIII, resistance to currant-lettuce aphid (Nasonovia ribisnigri) biotype Nr:0, and leaves having a solid main vein. The present invention also relates to a Lactuca sativa plant produced by growing the 81-01 RZ seed. The invention further relates to methods for producing the lettuce cultivar, represented by lettuce variety 81-01 RZ.

The disclosure relates to a series of independent human-induced non-transgenic mutations found at one or more of the Lip1 genes of a plant; plants having these mutations in one or more of their Lip1 genes; and a method of creating and finding similar and/or additional mutations of Lip1 by screening pooled and/or individual plants. The plants disclosed herein exhibit decreased lipase activity without having the inclusion of foreign nucleic acids in their genomes. Additionally, products produced from the plants disclosed herein exhibit increased hydrolytic and oxidative stability and increased shelf life without having the inclusion of foreign nucleic acids in their genomes.

The disclosure relates to a series of independent human-induced non-transgenic mutations found at one or more of the Lip1 genes of a plant; plants having these mutations in one or more of their Lip1 genes; and a method of creating and finding similar and/or additional mutations of Lip1 by screening pooled and/or individual plants. The plants disclosed herein exhibit decreased lipase activity without having the inclusion of foreign nucleic acids in their genomes. Additionally, products produced from the plants disclosed herein exhibit increased hydrolytic and oxidative stability and increased shelf life without having the inclusion of foreign nucleic acids in their genomes.

Presented herein, in certain embodiments, are nucleic acids and compositions for use in targeted gene editing.

This document provides materials and methods for generating oilseed (e.g., pennycress) plants that having low levels of erucic acid. For example, oilseed plants having reduced expression levels of one or more polypeptides involved in erucic acid metabolism (e.g., fatty acid elongase 1 (FAE1)), as well as materials and methods for making and using oilseed plants having low levels of erucic acid are provided.

The present invention relates to plants comprising a modified amount, activity or function of AGL11-like protein, wherein the plant is a member of plant family Cucurbitaceae or of species Solanum lycopersicum; characterized in that the plant is not a Solanum lycopersicum plant having a deletion from nucleotide 1042 to nucleotide 637 upstream of the ATG start codon of SEQ ID NO: 1.