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

机译:通过测序进行基因分型,可鉴定甘蓝(Brassica oleracea L.)的根部抗性QTL和参考基因组装配的修订

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摘要

Clubroot is a devastating disease caused by Plasmodiophora brassicae and results in severe losses of yield and quality in Brassica crops. Many clubroot resistance genes and markers are available in Brassica rapa but less is known in Brassica oleracea. 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 >5x coverage in the GBS data. Among those, 4,103 were credibly genotyped for all 78 F-2 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-2 (:) (3) progenies revealed two and single major QTLs for Race 2 and Race 9 of P. brassicae, respectively. The QTLs show similar locations to the previously reported CR loci for Race 4 in B. oleracea but are in different positions from any of the CR loci found in B. rapa. 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.
机译:马蹄根是由芸苔疟原虫引起的毁灭性疾病,导致芸苔属作物的产量和品质严重损失。在甘蓝型油菜中有许多根癌抗性基因和标记,但在甘蓝型油菜中却鲜为人知。在这里,我们应用了测序基因分型(GBS)技术来构建高分辨率遗传图谱并鉴定杆根抗性(CR)基因。使用GBS数据,针对两个亲本品系,一种抗性和一根对杆根的敏感品系,共鉴定出43,821个SNP,其中18,187个在GBS数据中显示> 5倍的覆盖率。其中,对所有78株F-2单株可靠地进行了4103种基因分型。这些标记聚类为9个连锁组,跨度为879.9 cM,平均间隔为1.15 cM。基于F-2(:)(3)后代的三轮根癌抗性测试的定量性状基因座(QTL)调查显示,芸苔假单胞菌第2种族和第9种族分别有两个和单个主要QTL。 QTL显示与先前报道的甘蓝型油菜第4种族的CR基因座相似的位置,但与在芜菁中发现的任何CR基因座的位置不同。在这项研究中,我们利用了两个参考基因组序列。本文开发的高分辨率遗传图谱使我们能够分别在02-12和TO1000DH基因组序列中重新定位37个和2个错误锚定的支架。我们的数据还支持将两个未锚定的3.3 Mb支架进一步定位到02-12基因组序列中。

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