Liu Ruiying, Luo Dangping, Scheffler Brian E, Hulse-Kemp Amanda M, Overlander-Chen Megan, Nandety Raja Sekhar, Fiedler Jason D, Chu Chenggen, Zhong Shaobin, Yang Shengming
Department of Plant Pathology, North Dakota State University, Fargo, ND, 58102, USA.
Genomics and Bioinformatics Research Unit, USDA-ARS, Stoneville, MS, 38776, USA.
Theor Appl Genet. 2025 May 27;138(6):127. doi: 10.1007/s00122-025-04916-w.
Fine mapping of the leaf rust susceptibility gene Sph1 identified a receptor-like kinase-encoding gene as a candidate and provided user-friendly markers for barley breeding. Caused by the biotrophic fungal pathogen Puccinia hordei, leaf rust is one of the important foliar diseases in barley. Although a few dominant genes for leaf rust resistance have been identified and cloned in barley, resistance conferred by major genes has been frequently defeated by the pathogen. A recessive resistance was identified in a spring barley accession using the P. hordei isolate VA90-34 which is virulent to most of major resistance genes. To localize this recessive resistance (hereafter named Susceptibility to P. hordei 1 or Sph1 indicating that the dominant allele confers disease susceptibility), we conducted fine mapping with an F population and molecular markers in the present study. The Sph1 gene was anchored near the telomere of the short arm of chromosome 3H, delimited within an ⁓560 kb region in the dominant parent. Of the six predicted genes in the Sph1 region, a gene encoding putative receptor-like kinase was selected as a candidate for functional validation. Therefore, our study provides a high-resolution genetic map and candidate for Sph1, building a foundation for the cloning of this important gene.
叶锈病感病基因Sph1的精细定位鉴定出一个编码类受体激酶的基因作为候选基因,并为大麦育种提供了实用的分子标记。叶锈病由活体营养型真菌病原体大麦柄锈菌引起,是大麦重要的叶部病害之一。尽管在大麦中已鉴定并克隆了一些抗叶锈病的显性基因,但主要基因赋予的抗性常常被病原菌克服。利用对大多数主要抗性基因具有毒性的大麦柄锈菌分离株VA90 - 34,在一个春大麦材料中鉴定出一种隐性抗性。在本研究中,为了定位这种隐性抗性(以下称为对大麦柄锈菌1的敏感性或Sph1,表明显性等位基因赋予感病性),我们利用一个F群体和分子标记进行了精细定位。Sph1基因定位于3H染色体短臂的端粒附近,在显性亲本中限定在一个约560 kb的区域内。在Sph1区域的6个预测基因中,一个编码假定类受体激酶的基因被选为功能验证的候选基因。因此,我们的研究提供了Sph1的高分辨率遗传图谱和候选基因,为克隆这个重要基因奠定了基础。