PubAg

Main content area

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

Author:
Karthikeyan, Adhimoolam, Li, Kai, Li, Cui, Yin, Jinlong, Li, Na, Yang, Yunhua, Song, Yingpei, Ren, Rui, Zhi, Haijian, Gai, Junyi
Source:
Theoretical and applied genetics 2018 v.131 no.2 pp. 461-476
ISSN:
0040-5752
Subject:
Glycine max, Soybean mosaic virus, chromosome mapping, chromosomes, crop production, disease resistance, dominant genes, gene segregation, genetic markers, genomics, heterozygosity, inbred lines, interleukins, marker-assisted selection, molecular cloning, parents, phenotype, proteins, quantitative polymerase chain reaction, resistance genes, reverse transcriptase polymerase chain reaction, selfing, sequence analysis, soybeans, China
Abstract:
KEY MESSAGE: 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, F₁, F₂ and the F₂:₇ 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.
Agid:
5900019