4.7 Article

Identification and Development of KASP Markers for Novel Mutant BnFAD2 Alleles Associated With Elevated Oleic Acid in Brassica napus

Journal

FRONTIERS IN PLANT SCIENCE
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2021.715633

Keywords

Brassica napus; seed oleic acid; quantitative trait loci; BnFAD2; kompetitive allele specific PCR

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Funding

  1. Youth Fund of the Natural Science Foundation of Zhejiang Province [LQ19C130002]
  2. Project of Mechanized Oilseed rape Breeding of the Downstream of Yangtze River [2018YFD0100602]
  3. Key Project of Novel Variety Breeding of Zhejiang Province [2016C02050-8]

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The FAD2 genes play a crucial role in determining the oleic acid content in rapeseed oil, with different alleles leading to variations in oil composition. Through QTL mapping and SNP markers, four QTL related to C18:1 content were identified, with BnFAD2.A05 and BnFAD2.C05 genes explaining a significant portion of the variation. Novel mutant alleles were found near specific protein motifs, resulting in higher oleic acid content in seed oil when combined. Competitive allele-specific PCR markers based on these mutations were successfully developed and validated, aiding in breeding for ultra-high oleic acid content in oilseed rape.
The fatty acid desaturase FAD2 genes are the main contributors to oleic acid content, and different FAD2 alleles can result in different oleic acid contents in rapeseed oil. Hence, identification of allelic variation in FAD2 is an extremely desirable breeding goal. By performing QTL mapping using 190 F-2:3 lines genotyped by genome-wide single nucleotide polymorphism (SNP) markers assayed by the Brassica 60 K Infinium BeadChip Array, four quantitative trait loci (QTL) for C18:1 content were mapped on chromosomes A01, A05, A09 and C05 over 3 years in a population segregating for oleic acid content. Two BnFAD2 genes on A05 and C05 were anchored within the QTL intervals, explaining 45-52 and 15-44% of the observed variation for C18:1 content. Sequence polymorphisms between the corresponding coding regions of the parental lines found two single-nucleotide polymorphisms (SNPs) in BnFAD2.A05 and BnFAD2.C05, respectively, which led to the amino acid changes (C421T and G1073E) in the corresponding proteins. The mutation sites of Bnfad2.A05 and Bnfad2.C05 alleles were located within the second H-box and near the third H-box motif of the protein, respectively, and were found to be novel mutant alleles. Lines resulting from the combination of these two alleles contained up to 88% oleic acid in their seed oil, compared with 63% in wild-type controls. Two competitive allele-specific PCR (KASP) markers based on these two mutation sites were successfully developed and validated in segregating F-2 populations. These markers will facilitate breeding for ultra-high seed oleic acid content in oilseed rape.

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