Suppr超能文献

大豆对大豆花叶病毒SC20株系抗性的精细定位及候选基因鉴定

Fine-mapping and identifying candidate genes conferring resistance to Soybean mosaic virus strain SC20 in soybean.

作者信息

Karthikeyan Adhimoolam, Li Kai, Li Cui, Yin Jinlong, Li Na, Yang Yunhua, Song Yingpei, Ren Rui, Zhi Haijian, Gai Junyi

机构信息

Soybean Research Institute, Nanjing Agricultural University, Nanjing, 210095, Jiangsu, China.

National Center for Soybean Improvement, Ministry of Agriculture, Nanjing, 210095, Jiangsu, China.

出版信息

Theor Appl Genet. 2018 Feb;131(2):461-476. doi: 10.1007/s00122-017-3014-1. Epub 2017 Nov 27.

Abstract

The Mendelian gene conferring resistance to Soybean mosaic virus Strain SC20 in soybean was fine-mapped onto a 79-kb segment on Chr.13 where two closely linked candidate genes were identified and qRT-PCR verified. Soybean mosaic virus (SMV) threatens the world soybean production, particularly in China. A country-wide SMV strain system composed of 22 strains was established in China, among which SC20 is a dominant strain in five provinces in Southern China. Resistance to SC20 was evaluated in parents, F, F and the F RIL (recombinant inbred line) population derived from a cross between Qihuang-1 (resistant) and NN1138-2 (susceptible). The segregation ratio of resistant to susceptible in the populations suggested a single dominant gene involved in the resistance to SC20 in Qihuang-1. A "partial genome mapping strategy" was used to map the resistance gene on Chromosome 13. Linkage analysis between 178 RILs and genetic markers showed that the SC20-resistance gene located at 3.9 and 3.8 cM to the flanking markers BARCSOYSSR_13_1099 and BARCSOYSSR_13_1185 on Chromosome 13. Subsequently, a residual heterozygote segregating population with 346 individuals was developed by selfing four plants heterozygous at markers adjacent to the tentative SC20-resistance gene; then, the candidate region was delimited to a genomic interval of approximately 79 kb flanked by the new markers gm-ssr_13-14 and gm-indel_13-3. Among the seven annotated candidate genes in this region, two genes, Glyma.13G194700 and Glyma.13G195100, encoding Toll Interleukin Receptor-nucleotide-binding-leucine-rich repeat resistance proteins were identified as candidate resistance genes by quantitative real-time polymerase chain reaction and sequence analysis. The two closely linked genes work together to cause the phenotypic segregation as a single Mendelian gene. These results will facilitate marker-assisted selection, gene cloning and breeding for the resistance to SC20.

摘要

赋予大豆对大豆花叶病毒SC20株系抗性的孟德尔基因被精细定位到13号染色体上一个79kb的区段,在该区段鉴定出两个紧密连锁的候选基因,并通过qRT-PCR验证。大豆花叶病毒(SMV)威胁着全球大豆生产,在中国尤为严重。中国建立了一个由22个株系组成的全国性SMV株系体系,其中SC20是中国南方五个省份的优势株系。在亲本、F1、F2以及由齐黄1号(抗病)和NN1138-2(感病)杂交衍生的F2重组自交系(RIL)群体中评估了对SC20的抗性。群体中抗病与感病的分离比例表明,齐黄1号中存在一个控制对SC20抗性的单显性基因。采用“部分基因组定位策略”将抗性基因定位到13号染色体上。对178个RILs与遗传标记进行连锁分析表明,SC20抗性基因位于13号染色体上侧翼标记BARCSOYSSR_13_1099和BARCSOYSSR_13_1185的3.9和3.8 cM处。随后,通过对与暂定的SC20抗性基因相邻标记处杂合的4株植株进行自交,构建了一个包含346个个体的残余杂合子分离群体;然后,候选区域被限定在由新标记gm-ssr_13-14和gm-indel_13-3侧翼的约79kb基因组区间内。在该区域的7个注释候选基因中,通过定量实时聚合酶链反应和序列分析,鉴定出两个编码Toll白细胞介素受体-核苷酸结合-富含亮氨酸重复序列抗性蛋白的基因Glyma.13G194700和Glyma.13G195100为候选抗性基因。这两个紧密连锁的基因共同作用,导致表型分离如同一个孟德尔基因。这些结果将有助于对SC20抗性的分子标记辅助选择、基因克隆和育种。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验