Genetic analysis and molecular mapping of resistance gene to Phakopsora pachyrhizi in soybean germplasm SX6907

被引:16
|
作者
Chen, Haifeng [1 ,2 ]
Zhao, Sheng [1 ,2 ,3 ]
Yang, Zhonglu [1 ,2 ]
Sha, Aihua [1 ,2 ]
Wan, Qiao [1 ,2 ]
Zhang, Chanjuan [1 ,2 ]
Chen, Limiao [1 ,2 ]
Yuan, Songli [1 ,2 ]
Qiu, Dezhen [1 ,2 ]
Chen, Shuilian [1 ,2 ]
Shan, Zhihui [1 ,2 ]
Zhou, Xin-an [1 ,2 ]
机构
[1] Chinese Acad Agr Sci, Oil Crops Res Inst, Wuhan 430062, Peoples R China
[2] Minist Agr, Key Lab Biol & Genet Improvement Oil Crops, Wuhan 430062, Peoples R China
[3] Chinese Acad Agr Sci, Grad Sch, Beijing 10081, Peoples R China
关键词
BULKED SEGREGANT ANALYSIS; CONFERS RESISTANCE; RUST RESISTANCE; SSR-MARKERS; IDENTIFICATION; LOCUS; CONFIRMATION; VIRULENCE; DETECT; ASSAY;
D O I
10.1007/s00122-015-2468-2
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
In this study, Rpp6907, a novel resistance gene/allele to Phakopsora pachyrhizi in soybean, was mapped in a 111.9-kb region, including three NBS-LRR type predicted genes, on chromosome 18. Soybean rust caused by Phakopsora pachyrhizi Sydow has been reported in numerous soybean-growing regions worldwide. The development of rust-resistant varieties is the most economical and environmentally safe method to control the disease. The Chinese soybean germplasm SX6907 is resistant to P. pachyrhizi and exhibits immune reaction compared with the known Rpp genes. These characteristics suggest that SX6907 may carry at least one novel Rpp gene/allele. Three F-2 populations from the crosses of SX6907 (resistant) and Tianlong 1, Zhongdou40, and Pudou11 (susceptible) were used to map the Rpp gene. Three resistance responses (immune, red-brown, and tan-colored lesion) were observed from the F-2 individuals. The segregation follows a ratio of 1(resistance):2(heterozygous):1(susceptible), indicating that the resistance in SX6907 is controlled by a single incomplete dominant gene (designated as Rpp6907). Results showed that Rpp6907 was mapped on soybean chromosome 18 (molecular linkage group G, MLG G) flanked by simple sequence repeat (SSR) markers SSR24 and SSR40 at a distance of 111.9 kb. Among the ten genes marked within this 111.9-kb region between the two markers, three genes (Glyma18g51930, Glyma18g51950, and Glyma18g51960) are nucleotide-binding site and leucine-rich repeat-type genes. These genes may be involved in recognizing the presence of pathogens and ultimately conferring resistance. Based on resistance spectrum analysis and mapping results, we inferred that Rpp6907 is a novel gene different from Rpp1 in PI 200492, PI 561356, PI 587880A, PI 587886, and PI 594538A, or a new Rpp1-b allele.
引用
收藏
页码:733 / 743
页数:11
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