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Identification of rice (Oryza sativa L.) genes involved in sheath blight resistance via a genome‐wide association study

Authors :
Xin Jing
Yueyang Liang
Yubi Huang
Xinyue Shu
Jun Zhu
Chen Lei
Ping Li
Ma Li
Aijun Wang
Shiquan Wang
Yuqi Jiang
Lingxia Wang
Aiping Zheng
Naoki Yamamoto
Chengzhi Jiao
Qiming Deng
Huainian Liu
Shuangcheng Li
Jinfeng Zhang
Ting Zou
Source :
Plant Biotechnology Journal
Publication Year :
2021
Publisher :
John Wiley and Sons Inc., 2021.

Abstract

Summary Rice sheath blight (RSB) is an economically significant disease affecting rice yield worldwide. Genetic resistance to RSB is associated with multiple minor genes, with each providing a minor phenotypic effect, but the underlying dominant resistance genes remain unknown. A genome‐wide association study (GWAS) of 259 diverse rice varieties, with genotypes based on a single nucleotide polymorphism (SNP) and haplotype, was conducted to assess their sheath blight reactions at three developmental stages (seedlings, tillering and booting). A total of 653 genes were correlated with sheath blight resistance, of which the disease resistance protein RPM1 (OsRSR1) and protein kinase domain‐containing protein (OsRLCK5) were validated by overexpression and knockdown assays. We further found that the coiled‐coil (CC) domain of OsRSR1 (OsRSR1‐CC) and full‐length OsRLCK5 interacted with serine hydroxymethyltransferase 1 (OsSHM1) and glutaredoxin (OsGRX20), respectively. It was found that OsSHM1, which has a role in the reactive oxygen species (ROS) burst, and OsGRX20 enhanced the antioxidation ability of plants. A regulation model of the new RSB resistance though the glutathione (GSH)‐ascorbic acid (AsA) antioxidant system was therefore revealed. These results enhance our understanding of RSB resistance mechanisms and provide better gene resources for the breeding of disease resistance in rice.

Details

Language :
English
ISSN :
14677652 and 14677644
Volume :
19
Issue :
8
Database :
OpenAIRE
Journal :
Plant Biotechnology Journal
Accession number :
edsair.doi.dedup.....8e39eefaa03e6991b6939cd67b952f3f