Genotyping-by-sequencing map permits identification of clubroot resistance QTLs and revision of the reference genome assembly in cabbage ( <i>Brassica oleracea</i> L.)

다국어 초록 (Multilingual Abstract)

<P>Clubroot is a devastating disease caused by <I>Plasmodiophora brassicae</I> and results in severe losses of yield and quality in <I>Brassica</I> crops. Many clubroot resistance genes and markers are available in <I>Brassica rapa</I> but less is known in <I>Brassica oleracea.</I> Here, we applied the genotyping-by-sequencing (GBS) technique to construct a high-resolution genetic map and identify clubroot resistance (CR) genes. A total of 43,821 SNPs were identified using GBS data for two parental lines, one resistant and one susceptible lines to clubroot, and 18,187 of them showed >5× coverage in the GBS data. Among those, 4,103 were credibly genotyped for all 78 F<SUB>2</SUB> individual plants. These markers were clustered into nine linkage groups spanning 879.9 cM with an average interval of 1.15 cM. Quantitative trait loci (QTLs) survey based on three rounds of clubroot resistance tests using F<SUB>2</SUB><SUB>:</SUB><SUB>3</SUB> progenies revealed two and single major QTLs for Race 2 and Race 9 of <I>P. brassicae</I>, respectively. The QTLs show similar locations to the previously reported CR loci for Race 4 in <I>B. oleracea</I> but are in different positions from any of the CR loci found in <I>B. rapa</I>. We utilized two reference genome sequences in this study. The high-resolution genetic map developed herein allowed us to reposition 37 and 2 misanchored scaffolds in the 02–12 and TO1000DH genome sequences, respectively. Our data also support additional positioning of two unanchored 3.3 Mb scaffolds into the 02–12 genome sequence.</P>