McCartney C A, Brûlé-Babel A L, Lamari L, Somers D J
Department of Plant Science, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
Theor Appl Genet. 2003 Nov;107(7):1181-6. doi: 10.1007/s00122-003-1359-0. Epub 2003 Jul 26.
Septoria tritici blotch, caused by Mycosphaerella graminicola, is a serious foliar disease of wheat worldwide. Qualitative, race-specific resistance sources have been identified and utilized for resistant cultivar development. However, septoria tritici blotch resistant varieties have succumbed to changes in virulence of M. graminicola on at least three continents. The use of resistance gene pyramids may slow or prevent the breakdown of resistance. A clear understanding of the genetics of resistance and the identification of linked PCR-based markers will facilitate the recovery of wheat lines carrying multiple septoria tritici blotch resistance genes. The resistance gene in ST6 to isolate MG2 of M. graminicola was mapped with microsatellite markers in two populations, ST6/Erik and ST6/Katepwa. Bulk segregant analysis identified a marker on chromosome 4AL putatively linked to the resistance gene. A large linkage group was identified in each population using additional microsatellite markers mapping to chromosome 4AL. The resistance gene in ST6 mapped to the distal end of chromosome 4AL in each mapping population and was designated Stb7. Three of the microsatellite loci, Xwmc313, Xwmc219 and Xgwm160, mapped within 3.5 cM of Stb7; however, none flanked Stb7. Xwmc313 was the closest and mapped 0.3 and 0.5 cM from Stb7 in the crosses ST6/Katepwa and ST6/Erik, respectively. WMC313 will be very useful for marker-assisted selection of Stb7 in Canadian breeding programs because the ST6 allele of Xwmc313 was not identified in any of the Canadian common wheat cultivars tested.
由小麦壳针孢引起的小麦叶枯病是一种在全球范围内严重危害小麦叶片的病害。已鉴定出定性的、具有小种专化性的抗性资源,并将其用于抗性品种的培育。然而,至少在三大洲,抗小麦叶枯病的品种已因小麦壳针孢毒力的变化而不再抗病。使用抗性基因聚合体可能会减缓或防止抗性的丧失。对抗性遗传学的清晰理解以及基于PCR的连锁标记的鉴定,将有助于培育携带多个抗小麦叶枯病基因的小麦品系。利用微卫星标记在ST6/Erik和ST6/Katepwa这两个群体中对ST6中抗小麦壳针孢分离株MG2的抗性基因进行了定位。混合分组分析法鉴定出4AL染色体上一个可能与抗性基因连锁的标记。使用定位到4AL染色体上的其他微卫星标记,在每个群体中鉴定出一个大的连锁群。在每个定位群体中,ST6中的抗性基因都定位到4AL染色体的远端,并被命名为Stb7。三个微卫星位点Xwmc313、Xwmc219和Xgwm160定位在距Stb7 3.5 cM范围内;然而,没有一个位于Stb7两侧。Xwmc313距离最近,在ST6/Katepwa和ST6/Erik杂交组合中分别距Stb7 0.3 cM和0.5 cM。WMC313对于加拿大育种项目中Stb7的标记辅助选择将非常有用,因为在所测试的任何加拿大普通小麦品种中都未鉴定出Xwmc313的ST6等位基因。