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大豆细菌性斑点病抗性基因的精细定位。

Fine mapping of a resistance gene to bacterial leaf pustule in soybean.

机构信息

Department of Plant Science and Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul, 151-921, Korea.

出版信息

Theor Appl Genet. 2010 May;120(7):1443-50. doi: 10.1007/s00122-010-1266-0. Epub 2010 Jan 20.

Abstract

Soybean bacterial leaf pustule (BLP) is a prevalent disease caused by Xanthomonas axonopodis pv. glycines. Fine mapping of the BLP resistant gene, rxp, is needed to select BLP resistant soybean cultivars by marker-assisted selection (MAS). We used a total of 227 recombinant inbred lines (RILs) derived from a cross between 'Taekwangkong' (BLP susceptible) and 'Danbaekkong' (BLP resistant) for rxp fine mapping and two different sets of near isogenic lines (NILs) from Hwangkeumkong x SS2-2 and Taekwangkong x SS2-2 were used for confirmation. Using sequences between Satt372 and Satt486 flanking rxp from soybean genome sequences, eight simple sequence repeats (SSR) and two single nucleotide polymorphism (SNP) markers were newly developed in a 6.2-cM interval. Linkage mapping with the RILs and NILs allowed us to map the rxp region with high resolution. The genetic order of all markers was completely consistent with their physical order. QTL analysis by comparison of the BLP phenotyping data with all markers showed rxp was located between SNUSSR17_9 and SNUSNP17_12. Gene annotation analysis of the 33 kb region between SNUSSR17_9 and SNUSNP17_12 suggested three predicted genes, two of which could be candidate genes of BLP resistance: membrane protein and zinc finger protein. Candidate genes showed high similarity with their paralogous genes, which were located on the duplicated regions obtaining BLP resistance QTLs. High-resolution map in rxp region with eight SSR and two SNP markers will be useful for not only MAS of BLP resistance but also characterization of rxp.

摘要

大豆细菌性斑疹病(BLP)是由黄单胞菌属大豆致病变种引起的一种常见病害。通过标记辅助选择(MAS)选择抗 BLP 大豆品种,需要对 BLP 抗性基因 rxp 进行精细定位。我们共使用了 227 个来自 'Taekwangkong'(BLP 敏感)和 'Danbaekkong'(BLP 抗性)杂交的重组自交系(RIL)进行 rxp 精细定位,还使用了来自 Hwangkeumkong x SS2-2 和 Taekwangkong x SS2-2 的两套不同的近等基因系(NIL)进行确认。利用大豆基因组序列中围绕 rxp 的 Satt372 和 Satt486 侧翼序列,在 6.2-cM 区间内新开发了 8 个简单序列重复(SSR)和 2 个单核苷酸多态性(SNP)标记。利用 RIL 和 NIL 进行连锁作图,可以对 rxp 区域进行高分辨率定位。所有标记的遗传顺序与物理顺序完全一致。通过将 BLP 表型数据与所有标记进行比较进行 QTL 分析,结果表明 rxp 位于 SNUSSR17_9 和 SNUSNP17_12 之间。对 SNUSSR17_9 和 SNUSNP17_12 之间 33kb 区域的基因注释分析表明,有 3 个预测基因,其中 2 个可能是 BLP 抗性的候选基因:膜蛋白和锌指蛋白。候选基因与位于获得 BLP 抗性 QTL 的重复区域的其同源基因具有高度相似性。带有 8 个 SSR 和 2 个 SNP 标记的 rxp 区域的高分辨率图谱不仅对 BLP 抗性的 MAS 有用,而且对 rxp 的表征也有用。

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