Genetic markers for myb28
US-2017137897-A1 · May 18, 2017 · US
US10385353B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10385353-B2 |
| Application number | US-201615359429-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 22, 2016 |
| Priority date | Sep 13, 2012 |
| Publication date | Aug 20, 2019 |
| Grant date | Aug 20, 2019 |
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The invention provides compositions and methods relating to the elevation of glucoraphanin compared to standard Brassica oleracea varieties. The invention also relates to the production of hybrid varieties having desired glucosinolate contents. The invention further provides plants, plant parts, and seeds comprising such traits and comprising a Myb28 allele from Brassica villosa that is not genetically linked to an ELONG allele from Brassica villosa.
Opening claim text (preview).
What is claimed is: 1. A method for obtaining a Brassica plant comprising a desired glucosinolate composition, said method comprising: (a) obtaining a Brassica plant heterozygous for a Myb28 allele from Brassica villosa that confers elevated glucosinolates relative to a Brassica oleracea plant lacking the Myb28 allele and is genetically linked in the plant to an elongation (ELONG) allele from Brassica villosa; (b) obtaining progeny of the plant; and (c) selecting at least a first progeny plant in which recombination has occurred such that the progeny comprises the Myb28 allele but not the ELONG allele from Brassica villosa , wherein the progeny plant possesses a desired glucosinolate composition as a result of the presence of the Myb28 allele but not the ELONG allele from Brassica villosa. 2. The method of claim 1 , wherein selecting the progeny plant comprises identifying a progeny plant that (1) comprises a genetic marker genetically linked to the Myb28 allele in Brassica villosa and/or lacks a genetic marker present at the corresponding locus in said Brassica plant, and (2) lacks a genetic marker genetically linked to the ELONG allele from Brassica villosa and/or comprises a genetic marker present at the corresponding locus from said Brassica plant. 3. The method of claim 2 , wherein selecting a progeny plant comprises detecting a polymorphism that is found in the genome of said plant flanked by the complements of SEQ ID NO:1 and SEQ ID NO:2. 4. The method of claim 3 , wherein the allele(s) are detected by a PCR-based method using oligonucleotide primer pair(s). 5. The method of claim 2 , wherein selecting a progeny plant comprises detecting in said plant a locus that is polymorphic between SEQ ID NO:8 and SEQ ID NO:9. 6. The method of claim 1 , wherein the Brassica plant is a B. oleracea plant.
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