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利用重组自交系和次级群体对一个控制[此处缺失具体控制对象]的抗性基因进行精细定位。

Fine Mapping of a Resistance Gene that Controls Using Recombinant Inbred Lines and Secondary Populations.

作者信息

Niu Jingping, Guo Na, Sun Jutao, Li Lihong, Cao Yongce, Li Shuguang, Huang Jianli, Zhao Jinming, Zhao Tuanjie, Xing Han

机构信息

National Center for Soybean Improvement, Key Laboratory of Biology and Genetics and Breeding for Soybean, Ministry of Agriculture, State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural UniversityNanjing, China.

出版信息

Front Plant Sci. 2017 Apr 11;8:538. doi: 10.3389/fpls.2017.00538. eCollection 2017.

Abstract

Phytophthora root rot (PRR), caused by , has negative effects on soybean yield in China and can be controlled by identifying germplasm resources with resistance genes. In this study, the resistance locus in the soybean line Meng8206 was mapped using two mapping populations. Initial mapping was realized using two recombinant inbred line (RIL) populations and included 103 F RILs derived from a cross of Meng8206 × Linhedafenqing, including 2600 bin markers, and 130 F RILs derived from a cross of Meng8206 × Zhengyang148, including 2267 bin markers. Subsequently, a 159 F secondary population derived from a cross of Meng8206 × Linmeng6-46, were used to fine map this locus using SSR markers. Finally, the resistance locus from Meng8206 was fine mapped to a 278.7 kb genomic region flanked by SSR markers SSRSOYN-25 and SSRSOYN-44 at a genetic distance of 1.6 and 1.0 cM on chromosome 3 (Chr. 03). Real-time RT-PCR analysis of the possible candidate genes showed that three genes (, and ) are likely involved in PRR resistance. These results will serve as a basis for cloning, transferring of resistant genes and breeding of -resistant soybean cultivars through marker-assisted selection.

摘要

由[病原体名称未给出]引起的疫霉根腐病(PRR)对中国大豆产量有负面影响,通过鉴定具有抗性基因的种质资源可对其进行控制。在本研究中,利用两个作图群体对大豆品系蒙8206中的抗性位点进行了定位。初步定位使用了两个重组自交系(RIL)群体,包括由蒙8206×临河大粉青杂交产生的103个F代RIL,包含2600个bin标记,以及由蒙8206×正阳148杂交产生的130个F代RIL,包含2267个bin标记。随后,利用由蒙8206×临蒙6 - 46杂交产生并包含159个个体的次级群体,使用SSR标记对该位点进行精细定位。最后,将蒙8206的抗性位点精细定位到3号染色体(Chr. 03)上SSR标记SSRSOYN - 25和SSRSOYN - 44侧翼的一个278.7 kb基因组区域,遗传距离分别为1.6和1.0 cM。对可能的候选基因进行实时RT - PCR分析表明,三个基因([基因名称未给出])可能参与了对疫霉根腐病的抗性。这些结果将为通过标记辅助选择克隆、转移抗性基因以及培育抗疫霉根腐病大豆品种奠定基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4b8/5387331/802fb81577d3/fpls-08-00538-g001.jpg

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