Ping Jieqing, Fitzgerald Joshua C, Zhang Chunbao, Lin Feng, Bai Yonghe, Wang Dechun, Aggarwal Rajat, Rehman Maqsood, Crasta Oswald, Ma Jianxin
Department of Agronomy, Purdue University, West Lafayette, IN, 47907, USA.
Bayer CropScience LP, Research Triangle Park, NC, 27709, USA.
Theor Appl Genet. 2016 Feb;129(2):445-51. doi: 10.1007/s00122-015-2638-2. Epub 2015 Dec 10.
Rps11 confers excellent resistance to predominant Phytophthora sojae isolates capable of defeating major Rps genes deployed into soybean production, representing a novel source of resistance for soybean cultivar enhancement.
Phytophthora root and stem rot (PRSR), caused by the soil-borne pathogen Phytophthora sojae, is a devastating disease of soybean [Glycine max (L.) Merr.] throughout the world. Deploying resistant soybean cultivars is the most effective and environmentally friendly approach to managing this disease. The soybean landrace PI 594527 was found to carry excellent resistance to all P. sojae isolates examined, some of which were capable of overcoming the major Rps genesp, such as Rps1-k, Rps1-c, and Rps3-a, predominantly used for soybean protection in the past decades. A mapping population consisting of 58 F2 individuals and 209 F2:3 families derived from a cross between PI 594527 and the susceptible cultivar 'Williams' was used to characterize the inheritance pattern of the resistance to P. soja (Rps) in PI 594527. It was found that the resistance was conferred by a single Rps gene, designated Rps11, which was initially defined as an ~5 Mb genomic region at the beginning of chromosome 7 by bulked segregant analysis (BSA) with a nucleotide polymorphism (SNP) chip comprising 7039 SNP markers. Subsequently, simple sequence repeat (SSR) markers in the defined region were used to genotype the F2:3 mapping population to map Rps11 to a 225.3 kb genomic region flanked by SSR markers BARCSOYSSR_07_0286 and BARCSOYSSR_07_0300, according to the soybean reference genome sequence. Particularly, an SSR marker (i.e., BARCSOYSSR_07_0295) was found to tightly co-segregate with Rps11 in the mapping population and can be effectively used for marker-assisted selection of this gene for development of resistant soybean cultivars.
Rps11对能克服大豆生产中主要Rps基因的大豆疫霉优势分离株具有优异抗性,是增强大豆品种抗性的新来源。
由土壤传播病原菌大豆疫霉引起的大豆根茎腐病(PRSR)是全球大豆[Glycine max (L.) Merr.]的毁灭性病害。种植抗病大豆品种是防治该病最有效且环保的方法。发现大豆地方品种PI 594527对所有检测的大豆疫霉菌株都具有优异抗性,其中一些菌株能够克服过去几十年主要用于大豆保护的主要Rps基因,如Rps1-k、Rps1-c和Rps3-a。利用由PI 594527与感病品种‘Williams’杂交产生的包含58个F2个体和209个F2:3家系的作图群体,来鉴定PI 594527对大豆疫霉(Rps)抗性的遗传模式。发现该抗性由一个单一的Rps基因Rps11控制,通过使用包含7039个单核苷酸多态性(SNP)标记的SNP芯片进行混合分离分析(BSA),最初将其定位在7号染色体起始处约5 Mb的基因组区域。随后,根据大豆参考基因组序列,使用定义区域内的简单序列重复(SSR)标记对F2:3作图群体进行基因分型,将Rps11定位到由SSR标记BARCSOYSSR_07_0286和BARCSOYSSR_07_0300侧翼的225.3 kb基因组区域。特别地,发现一个SSR标记(即BARCSOYSSR_07_0295)在作图群体中与Rps11紧密共分离,可有效用于该基因的标记辅助选择,以培育抗病大豆品种。