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中国大豆广谱抗性基因的遗传作图和分子特征。

Genetic Mapping and Molecular Characterization of a Broad-spectrum Resistance Gene in Chinese Soybean.

机构信息

National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

Institute of Pomology, Chinese Academy of Agricultural Sciences, Xingcheng 125100, China.

出版信息

Int J Mol Sci. 2019 Apr 12;20(8):1809. doi: 10.3390/ijms20081809.

DOI:10.3390/ijms20081809
PMID:31013701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6515170/
Abstract

Phytophthora root rot (PRR) causes serious annual soybean yield losses worldwide. The most effective method to prevent PRR involves growing cultivars that possess genes conferring resistance to Phytophthora sojae (Rps). In this study, QTL-sequencing combined with genetic mapping was used to identify in soybean cultivar Xiu94-11 resistance to all isolates tested, exhibiting broad-spectrum PRR resistance. Subsequent analysis revealed was located in the 242-kb genomic region spanning the locus. However, a phylogenetic investigation indicated Xiu94-11 carrying is distantly related to the cultivars containing , implying and have different origins. An examination of candidate genes revealed and share common nonsynonymous SNP and a 144-bp insertion in the sequence encoding a leucine-rich repeat (LRR) region. was considered to be the likely candidate gene of and . Sequence analyses confirmed that the 144-bp insertion caused by an unequal exchange resulted in two additional LRR-encoding fragments in the candidate gene. A marker developed based on the 144-bp insertion was used to analyze the genetic population and germplasm, and proved to be useful for identifying the and alleles. This study implies that the number of LRR units in the LRR domain may be important for PRR resistance in soybean.

摘要

大豆疫霉根腐病(PRR)在全球范围内导致严重的大豆年度减产。预防 PRR 的最有效方法是种植具有抗大豆疫霉菌(Rps)基因的品种。在本研究中,使用 QTL 测序结合遗传图谱定位到了大豆品种秀 94-11 中的一个 QTL,该 QTL 可赋予其对所有测试分离物的广谱 PRR 抗性。进一步分析表明,该 QTL 位于包含 基因的 242-kb 基因组区域内。然而,系统发育分析表明,携带 的秀 94-11 与含有 的品种远缘相关,暗示 和 具有不同的起源。对候选基因的分析表明, 和 共享常见的非同义 SNP 和 144-bp 插入,该插入位于编码富含亮氨酸重复(LRR)区域的序列中。 被认为是 的候选基因。序列分析证实,由不等交换引起的 144-bp 插入导致候选基因中额外编码两个 LRR 片段。基于 144-bp 插入开发的标记被用于分析遗传群体和种质资源,并且被证明可用于鉴定 和 等位基因。本研究表明,LRR 结构域中 LRR 单元的数量可能对大豆 PRR 抗性很重要。

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