4.7 Article

PmSN15218: A Potential New Powdery Mildew Resistance Gene on Wheat Chromosome 2AL

期刊

FRONTIERS IN PLANT SCIENCE
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2022.931778

关键词

wheat; powdery mildew; BSR-Seq; Pm4 loci; Pm-SN15218

资金

  1. Key R&D Program of Shandong Province (Major Science and Technology Innovation Project) [2021LZGC009]
  2. Shandong Provincial Scientific Innovation Project for Young Scholars of Universities [2019KJF026]

向作者/读者索取更多资源

Powdery mildew, caused by Blumeria graminis f. sp. tritici, is a devastating fungal disease affecting wheat worldwide. Identifying new resistance genes and breeding resistant varieties are effective strategies to combat this disease. Genetic and molecular analysis of the resistant breeding line SN15218 led to the discovery of the new resistance gene Pm-SN15218 located on chromosome 2AL.
Powdery mildew, caused by Blumeria graminis f. sp. tritici (Bgt), is a devastating fungal disease that seriously damages the yield and quality of wheat in many regions of the world. Identifying new resistance genes and breeding new resistant varieties are effective methods to control this disease. The breeding line SN15218 shows good resistance against powdery mildew. We, therefore, developed an F-2 population and 287 F-2:3 families crossed between SN15218 and the powdery mildew susceptible cultivar Huixianhong (HXH). Genetic analysis indicated that a single dominant gene, designated herein Pm-SN15218, conferred resistance to the Bgt isolate E09 in SN15218. Bulked segregant RNA-Seq (BSR-Seq) analysis revealed that Pm-SN15218 is located in a similar to 25-Mb interval on chromosome 2AL. Using the polymorphism information between SN15218 and HXH, we developed 13 polymerase chain reaction (PCR) markers and mapped this gene to a 0.5-cM genetic interval between the two flanking markers PmM12 and PmM14, corresponding to a 6.01-Mb physical region in the Chinese Spring reference genome. The results of molecular marker analysis, allelic tests of resistance spectrum, and DNA resequencing indicated that Pm-SN15218 is distinct from the known resistance gene Pm4b on 2AL.

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