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黄瓜茎部对白粉病抗性的分子图谱构建及候选基因分析

Molecular mapping and candidate gene analysis for resistance to powdery mildew in Cucumis sativus stem.

作者信息

Liu P N, Miao H, Lu H W, Cui J Y, Tian G L, Wehner T C, Gu X F, Zhang S P

机构信息

Institute of Vegetables and Flowers, , , China.

Department of Horticultural Science, , , USA.

出版信息

Genet Mol Res. 2017 Aug 31;16(3):gmr-16-03-gmr.16039680. doi: 10.4238/gmr16039680.

Abstract

Powdery mildew (PM) of cucumber (Cucumis sativus), caused by Podosphaera xanthii, is a major foliar disease worldwide and resistance is one of the main objectives in cucumber breeding programs. The resistance to PM in cucumber stem is important to the resistance for the whole plant. In this study, genetic analysis and gene mapping were implemented with cucumber inbred lines NCG-122 (with resistance to PM in the stem) and NCG-121 (with susceptibility in the stem). Genetic analysis showed that resistance to PM in the stem of NCG-122 was qualitative and controlled by a single-recessive nuclear gene (pm-s). Susceptibility was dominant to resistance. In the initial genetic mapping of the pm-s gene, 10 SSR markers were discovered to be linked to pm-s, which was mapped to chromosome 5 (Chr.5) of cucumber. The pm-s gene's closest flanking markers were SSR20486 and SSR06184/SSR13237 with genetic distances of 0.9 and 1.8 cM, respectively. One hundred and fifty-seven pairs of new SSR primers were exploited by the sequence information in the initial mapping region of pm-s. The analysis on the F mapping population using the new molecular markers showed that 17 SSR markers were confirmed to be linked to the pm-s gene. The two closest flanking markers, pmSSR27and pmSSR17, were 0.1 and 0.7 cM from pm-s, respectively, confirming the location of this gene on Chr.5. The physical length of the genomic region containing pm-s was 135.7 kb harboring 21 predicted genes. Among these genes, the gene Csa5G623470 annotated as encoding Mlo-related protein was defined as the most probable candidate gene for the pm-s. The results of this study will provide a basis for marker-assisted selection, and make the benefit for the cloning of the resistance gene.

摘要

由瓜单囊壳白粉菌引起的黄瓜白粉病是一种世界性的主要叶部病害,抗病性是黄瓜育种计划的主要目标之一。黄瓜茎对白粉病的抗性对整株植物的抗性很重要。在本研究中,利用黄瓜自交系NCG - 122(茎对白粉病有抗性)和NCG - 121(茎对白粉病敏感)进行了遗传分析和基因定位。遗传分析表明,NCG - 122茎对白粉病的抗性是定性的,由一个单隐性核基因(pm - s)控制。感病性对抗性为显性。在pm - s基因的初步遗传定位中,发现10个SSR标记与pm - s连锁,该基因被定位到黄瓜的5号染色体(Chr.5)上。pm - s基因最紧密的侧翼标记是SSR20486和SSR06184/SSR13237,遗传距离分别为0.9和1.8 cM。利用pm - s初步定位区域的序列信息开发了157对新的SSR引物。使用新的分子标记对F定位群体进行分析表明,有17个SSR标记被证实与pm - s基因连锁。两个最紧密的侧翼标记pmSSR27和pmSSR17分别距离pm - s 0.1和0.7 cM,证实了该基因在Chr.5上的位置。包含pm - s的基因组区域的物理长度为135.7 kb,含有21个预测基因。在这些基因中,注释为编码Mlo相关蛋白的基因CsaFiveG623470被确定为pm - s最可能的候选基因。本研究结果将为分子标记辅助选择提供依据,并有助于抗性基因的克隆。

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