Department of Agronomy, Iowa State University, Ames, IA, 50011-1010, USA.
Department of Agronomy, Shenyang Agricultural University, 120 Dongling Ave, Shenyang, Liaoning, 110866, China.
Theor Appl Genet. 2016 May;129(5):863-77. doi: 10.1007/s00122-015-2651-5. Epub 2016 Mar 7.
Using a combination of phenotypic screening and molecular, statistical, and linkage analyses, we have mapped a dominant soybean rust resistance gene in soybean PI 567104B. Asian soybean rust (SBR), caused by the fungus Phakopsora pachyrhizi Syd. and P. Syd., is one of the most economically important diseases that affect soybean production worldwide. A long-term strategy for minimizing the effects of SBR is the development of genetically resistant cultivars. The objectives of the study were to identify the location of a rust-resistance (Rpp) gene(s) in plant introduction (PI) 567104B, and to determine if the gene(s) in PI 567104B was different from previously mapped Rpp loci. The progeny of the cross of 'IAR 2001 BSR' × PI 567104B was phenotyped from field assays of the F 2:3 and F 4:5 generations and from a growth chamber assay of 253 F 5:6 recombinant inbred lines (RILs). For the growth chamber, the phenotyping was conducted by inoculation with a purified 2006 fungal isolate from Mississippi. A resistance gene locus on PI 567104B was mapped to a region containing the Rpp6 locus on chromosome 18. The high level of resistance of F 1 plants from two other crosses with PI 567104B as one of the parents indicated that the gene from PI 567104B was dominant. The interval containing the gene is flanked by the simple sequence repeat (SSR) markers Satt131 and Satt394, and includes the SSR markers BARCSOYSSR_18_0331 and BARCSOYSSR_18_0380. The results also indicated that the resistance gene from PI 567104B is different from the Rpp1 to the Rpp4 genes previously identified. To determine if the gene from PI 567104B is different from the Rpp6 gene from PI 567102B, additional research will be required.
利用表型筛选和分子、统计和连锁分析相结合的方法,我们在大豆 PI 567104B 中定位了一个显性大豆锈病抗性基因。亚洲大豆锈病(SBR)由真菌 Phakopsora pachyrhizi Syd. 和 P. Syd. 引起,是全球影响大豆生产的最重要的经济疾病之一。减少 SBR 影响的长期策略是开发具有遗传抗性的品种。本研究的目的是确定植物引种(PI)567104B 中锈病抗性(Rpp)基因的位置,并确定 PI 567104B 中的基因是否与先前定位的 Rpp 基因座不同。通过对 F 2:3 和 F 4:5 世代的田间试验和 253 个 F 5:6 重组自交系(RIL)的生长室试验对 'IAR 2001 BSR'×PI 567104B 的后代进行表型分析。对于生长室,通过接种来自密西西比州的 2006 年真菌分离物进行表型分析。PI 567104B 上的一个抗性基因座被定位到包含 18 号染色体上 Rpp6 基因座的区域。另外两个与 PI 567104B 作为亲本之一的杂交 F 1 植物的高水平抗性表明,来自 PI 567104B 的基因是显性的。包含该基因的区间由简单重复序列(SSR)标记 Satt131 和 Satt394 侧翼,包括 SSR 标记 BARCSOYSSR_18_0331 和 BARCSOYSSR_18_0380。结果还表明,来自 PI 567104B 的抗性基因与先前鉴定的 Rpp1 至 Rpp4 基因不同。为了确定来自 PI 567104B 的基因是否与来自 PI 567102B 的 Rpp6 基因不同,还需要进一步研究。