4.7 Article

Fine mapping of a stripe rust resistance gene YrZM175 in bread wheat

Journal

THEORETICAL AND APPLIED GENETICS
Volume 135, Issue 10, Pages 3485-3496

Publisher

SPRINGER
DOI: 10.1007/s00122-022-04195-9

Keywords

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Funding

  1. National Natural Science Foundation of China [31971929, 31961143007]
  2. National Key Research and Development Program of China [2016YFD0101802, 2016YFE0108600]
  3. CAAS Science and Technology Innovation Program

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In this study, we conducted fine mapping and candidate gene analysis of the stripe rust resistance gene YrZM175 in the Chinese wheat cultivar Zhongmai 175. Through bulked segregant RNA-seq analysis, we identified a genomic interval on chromosome arm 2AL where YrZM175 is located and predicted a potential candidate gene for map-based cloning. Collinearity analysis and gene expression level analysis further supported the identification of the candidate gene. The fine mapping of YrZM175 provides a solid foundation for functional gene analysis and marker-assisted selection for improved stripe rust resistance in wheat.
Key message A stripe rust resistance gene YrZM175 in Chinese wheat cultivar Zhongmai 175 was mapped to a genomic interval of 636.4 kb on chromosome arm 2AL, and a candidate gene was predicted. Stripe rust, caused by Puccinia striiformis f. sp. tritici (PST), is a worldwide wheat disease that causes large losses in production. Fine mapping and cloning of resistance genes are important for accurate marker-assisted breeding. Here, we report the fine mapping and candidate gene analysis of stripe rust resistance gene YrZM175 in a Chinese wheat cultivar Zhongmai 175. Fifteen F-1, 7,325 F-2 plants and 117 F-2:3 lines derived from cross Avocet S/Zhongmai 175 were inoculated with PST race CYR32 at the seedling stage in a greenhouse, and F-2:3 lines were also evaluated for stripe rust reaction in the field using mixed PST races. Bulked segregant RNA-seq (BSR-seq) analyses revealed 13 SNPs in the region 762.50-768.52 Mb on chromosome arm 2AL. By genome mining, we identified SNPs and InDels between the parents and contrasting bulks and mapped YrZM175 to a 0.72-cM, 636.4-kb interval spanned by YrZM175-InD1 and YrZM175-InD2 (763,452,916-764,089,317 bp) including two putative disease resistance genes based on IWGSC RefSeq v1.0. Collinearity analysis indicated similar target genomic intervals in Chinese Spring, Aegilops tauschii (2D: 647.7-650.5 Mb), Triticum urartu (2A: 750.7-752.3 Mb), Triticum dicoccoides (2A: 771.0-774.5 Mb), Triticum turgidum (2B: 784.7-788.2 Mb), and Triticum aestivum cv. Aikang 58 (2A: 776.3-778.9 Mb) and Jagger (2A: 789.3-791.7 Mb). Through collinearity analysis, sequence alignments of resistant and susceptible parents and gene expression level analysis, we predicted TRITD2Bv1G264480 from Triticum turgidum to be a candidate gene for map-based cloning of YrZM175. A gene-specific marker for TRITD2Bv1G264480 co-segregated with the resistance gene. Molecular marker analysis and stripe rust response data revealed that YrZM175 was different from genes Yr1, Yr17, Yr32, and YrJ22 located on chromosome 2A. Fine mapping of YrZM175 lays a solid foundation for functional gene analysis and marker-assisted selection for improved stripe rust resistance in wheat.

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