Identification of a new Rsg1 allele conferring resistance to multiple greenbug biotypes from barley accessions PI 499276 and PI 566459

Xiangyang Xu, Dolores Mornhinweg, Guihua Bai, Genqiao Li, Ruolin Bian, Amy Bernardo, J. Scott Armstrong
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Abstract

Greenbug [Schizaphis graminum (Rondani)] is a major insect pest that significantly affects barley production worldwide. The identification of novel greenbug resistance genes is crucial for sustainable barley production and global food security. To identify greenbug resistance genes from a US breeding line PI 499276 and a Chinese cultivar PI 566459, two F6:7 recombinant inbred line (RIL) populations developed from crosses Weskan × PI 499276 and Weskan × PI 566459 were phenotyped for responses to greenbug biotype E and genotyped using genotyping-by-sequencing (GBS). Linkage analysis using single nucleotide polymorphism and kompetitive allele-specific polymorphism (KASP) markers delimited the greenbug resistance genes from PI 499276 and PI 566459 to a 1.2 Mb genomic region between 666.5 and 667.7 Mb on the long arm of chromosome 3H in the Morex Hordeum vulgare r1 reference sequence. Allelism tests based on responses of four F2 populations to greenbug biotype E indicated that the greenbug resistance gene in PI 499276 and PI 566459 is either allelic or very close to Rsg1. Given that PI 499276 and PI 566459 shared the same unique resistance pattern to a set of 14 greenbug biotypes, which is different from those of other Rsg1 alleles, they carry a new Rsg1 allele. The greenbug resistance genes in Post 90, PI 499276/PI 566459, and WBDC 336 were designated as Rsg1.a1, Rsg1.a2, and Rsg1.a3, respectively. KASP markers KASP-Rsg1a3-1, KASP-Rsg1a3-2, and KASP160 can be used to tag Rsg1.a2 in barley breeding.
从大麦登录品种 PI 499276 和 PI 566459 中鉴定出一个新的 Rsg1 等位基因,该等位基因赋予大麦对多种青虫生物型的抗性
绿虫(Schizaphis graminum, Rondani)是一种严重影响全球大麦生产的主要害虫。新绿虫抗性基因的鉴定对大麦的可持续生产和全球粮食安全至关重要。为鉴定美国品种PI 499276和中国品种PI 566459的绿虫抗性基因,利用Weskan × PI 499276和Weskan × PI 566459杂交获得的两个F6:7重组自交系(RIL)群体对绿虫E型的反应进行了表型分析,并采用基因分型测序(GBS)技术进行了基因分型。利用单核苷酸多态性和竞争等位基因特异性多态性(KASP)标记进行连锁分析,将绿虫抗性基因从PI 499276和PI 566459定位到Morex Hordeum vulgare r1参考序列3H染色体长臂上666.5 ~ 667.7 Mb之间的1.2 Mb基因组区域。对4个F2群体对绿虫E型反应的等位基因测试表明,PI 499276和PI 566459的绿虫抗性基因要么是等位基因,要么与Rsg1非常接近。鉴于PI 499276和PI 566459对一组14种绿虫生物型具有不同于其他Rsg1等位基因的独特抗性模式,它们携带了一个新的Rsg1等位基因。90后绿虫抗性基因、PI 499276/PI 566459和WBDC 336分别命名为Rsg1。a1, Rsg1。a2和Rsg1。分别a3。KASP标记物KASP- rsg13a3 -1、KASP- rsg13a3 -2和KASP160可用于标记Rsg1。大麦育种A2。
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