4.7 Article

Fine mapping of a Phytophthora-resistance gene RpsWY in soybean (Glycine max L.) by high-throughput genome-wide sequencing

期刊

THEORETICAL AND APPLIED GENETICS
卷 130, 期 5, 页码 1041-1051

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SPRINGER
DOI: 10.1007/s00122-017-2869-5

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资金

  1. National Natural Science Foundation of China [30971814]
  2. China Agricultural Research System [CARS-04-PS09]
  3. Science and Technology Projects of Guangdong Province [2011A020102010]
  4. Project of Molecular Design Breeding for Major Economic Crops [2016yfd0101901]
  5. Research Project of the State Key Laboratory of Agricultural and Biological Resources Protection and Utilization in Subtropics [4100-M13024]

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Using a combination of phenotypic screening, genetic and statistical analyses, and high-throughput genome-wide sequencing, we have finely mapped a dominant Phytophthora resistance gene in soybean cultivar Wayao. Phytophthora root rot (PRR) caused by Phytophthora sojae is one of the most important soil-borne diseases in many soybean-production regions in the world. Identification of resistant gene(s) and incorporating them into elite varieties are an effective way for breeding to prevent soybean from being harmed by this disease. Two soybean populations of 191 F-2 individuals and 196 F-7:8 recombinant inbred lines (RILs) were developed to map Rps gene by crossing a susceptible cultivar Huachun 2 with the resistant cultivar Wayao. Genetic analysis of the F-2 population indicated that PRR resistance in Wayao was controlled by a single dominant gene, temporarily named RpsWY, which was mapped on chromosome 3. A high-density genetic linkage bin map was constructed using 3469 recombination bins of the RILs to explore the candidate genes by the high-throughput genome-wide sequencing. The results of genotypic analysis showed that the RpsWY gene was located in bin 401 between 4466230 and 4502773 bp on chromosome 3 through line 71 and 100 of the RILs. Four predicted genes (Glyma03g04350, Glyma03g04360, Glyma03g04370, and Glyma03g04380) were found at the narrowed region of 36.5 kb in bin 401. These results suggest that the high-throughput genome-wide resequencing is an effective method to fine map PRR candidate genes.

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