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Genetic dissection and identification of stripe rust resistance genes in the wheat cultivar Lanhangxuan 121, a cultivar selected from a space mutation population.

Authors :
Wu, Qimeng
Liu, Lei
Zhang, Dandan
Li, Chenchen
Nie, Ruiqi
Duan, Jiangli
Wan, Jufen
Zhao, Jiwen
Cao, Jianghao
Liu, Dan
Liu, Shengjie
Wang, Qilin
Zheng, Weijun
Yao, Qiang
Kang, Zhensheng
Zhang, Wentao
Du, Jiuyuan
Han, Dejun
Wang, Changfa
Wu, Jianhui
Source :
Molecular Breeding; Mar2024, Vol. 44 Issue 3, p1-22, 22p
Publication Year :
2024

Abstract

Stripe rust is a devastating disease of wheat worldwide. Chinese wheat cultivar Lanhangxuan 121 (LHX121), selected from an advanced line L92-47 population that had been subjected to space mutation breeding displayed a consistently higher level of resistance to stipe rust than its parent in multiple field environments. The aim of this research was to establish the number and types of resistance genes in parental lines L92-47 and LHX121 using separate segregating populations. The first population developed from a cross between LHX121 and susceptible cultivar Xinong 822 comprised 278 F<subscript>2:3</subscript> lines. The second validation population comprised 301 F<subscript>2:3</subscript> lines from a cross between L92-47 and susceptible cultivar Xinong 979. Lines of two population were evaluated for stripe rust response at three sites during the 2018–2020 cropping season. Affymetrix 660 K SNP arrays were used to genotype the lines and parents. Inclusive composite interval mapping detected QTL QYrLHX.nwafu-2BS, QYrLHX.nwafu-3BS, and QYrLHX.nwafu-5BS for resistance in all three environments. Based on previous studies and pedigree information, QYrLHX.nwafu-2BS and QYrLHX.nwafu-3BS were likely to be Yr27 and Yr30 that are present in the L92-47 parent. QYrLHX.nwafu-5BS (YrL121) detected only in LHX121 was mapped to a 7.60 cM interval and explained 10.67–22.57% of the phenotypic variation. Compared to stripe rust resistance genes previously mapped to chromosome 5B, YrL121 might be a new adult plant resistance QTL. Furthermore, there were a number of variations signals using 35 K SNP array and differentially expressed genes using RNA-seq between L92-47 and LHX121 in the YrL121 region, indicating that they probably impair the presence and/or function of YrL121. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13803743
Volume :
44
Issue :
3
Database :
Complementary Index
Journal :
Molecular Breeding
Publication Type :
Academic Journal
Accession number :
176354058
Full Text :
https://doi.org/10.1007/s11032-024-01461-0