Trabanco Noemí, Campa Ana, Ferreira Juan José
Plant Genetic Program, SERIDA, Asturias, Spain.
Plant Genome. 2015 Jul;8(2):eplantgenome2014.10.0079. doi: 10.3835/plantgenome2014.10.0079.
Anthracnose caused by Colletotrichum lindemuthianum (Sacc. & Magnus) Lams.-Scrib. is a major disease affecting common bean (Phaseolus vulgaris L.) crops worldwide. Response to five C. lindemuthianum isolates, classified as races 3, 6, 7, 38, and 73, were analyzed in 156 F families derived from the cross between line SEL1308 and cultivar Michigan Dark Red Kidney (MDRK). SEL1308 was resistant to all five races, while MDRK was susceptible to all except for race 73. Segregation ratio for response to races 3 and 7 indicated that single dominant genes were responsible for the resistance reaction to each race. Recombination between both race-specific genes was observed and no linkage was found with any of the molecular markers tagging Co-genes or clusters previously described. Linkage analyses allowed the location of both genes at the beginning of linkage group (LG) Pv03, a region tentatively named as Co-17. Segregation ratio for response to races 6 and 38 indicated that two dominant and independent genes conferred resistance to these races. Contingency tests and subpopulation analyses suggested the implication of one region on LG Pv08, corresponding to the Co-4 cluster, and the Co-17 region. For reaction to race 73, the most likely scenario was that two dominant and independent genes conferred resistance: Co-1 in MDRK and Co-4 in SEL1308. Results indicated that, in addition to Co-4 , SEL1308 carries resistance genes located at the beginning of LG Pv03, in which no anthracnose resistance genes were previously mapped. In silico analysis revealed the presence of seven genes codifying typical resistance proteins (R-proteins) in the underlying physical position of the Co-17 region.
由菜豆炭疽菌(Colletotrichum lindemuthianum (Sacc. & Magnus) Lams.-Scrib.)引起的炭疽病是一种影响全球普通菜豆(Phaseolus vulgaris L.)作物的主要病害。对156个F家系进行了分析,这些家系来自品系SEL1308与品种密歇根深红肾豆(MDRK)的杂交,分析了它们对5个菜豆炭疽菌分离株(分类为小种3、6、7、38和73)的反应。SEL1308对所有5个小种都具有抗性,而MDRK除对小种73外对其他小种均敏感。对小种3和7反应的分离比例表明,单个显性基因决定了对每个小种的抗性反应。观察到两个小种特异性基因之间的重组,并且未发现与先前描述的标记Co基因或簇的任何分子标记存在连锁关系。连锁分析将这两个基因定位在连锁群(LG)Pv03的起始位置,该区域暂命名为Co-17。对小种6和38反应的分离比例表明,两个显性且独立的基因赋予了对这些小种的抗性。列联检验和亚群分析表明LG Pv08上的一个区域(对应于Co-4簇)和Co-17区域有影响。对于对小种73的反应,最可能的情况是两个显性且独立的基因赋予抗性:MDRK中的Co-1和SEL1308中的Co-4。结果表明,除了Co-4之外,SEL1308还携带位于LG Pv03起始位置的抗性基因,该区域之前未定位过炭疽病抗性基因。电子分析揭示了在Co-17区域的潜在物理位置存在7个编码典型抗性蛋白(R蛋白)的基因。