State Key Laboratory for Agrobiotechnology, China Agricultural University, Beijing, 100193, People's Republic of China.
Theor Appl Genet. 2010 Nov;121(8):1613-21. doi: 10.1007/s00122-010-1414-6. Epub 2010 Aug 5.
Powdery mildew caused by Blumeria graminis f. sp. tritici is one of the most important wheat diseases worldwide and breeding for resistance using diversified disease resistance genes is the most promising approach to prevent outbreaks of powdery mildew. A powdery mildew resistance gene, originating from wild emmer wheat (Triticum turgidum var. dicoccoides) accessions collected from Israel, has been transferred into the hexaploid wheat line 3D232 through crossing and backcrossing. Inoculation results with 21 B. graminis f. sp. tritici races indicated that 3D232 is resistant to all of the powdery mildew isolates tested. Genetic analyses of 3D232 using an F(2) segregating population and F(3) families indicated that a single dominant gene, Ml3D232, confers resistance in the host seedling stage. By applying molecular markers and bulked segregant analysis (BSA), we have identified polymorphic simple sequence repeats (SSR), expressed sequence tags (EST) and derived sequence tagged site (STS) markers to determine that the Ml3D232 is located on chromosome 5BL bin 0.59-0.76. Comparative genetic analyses using mapped EST markers and genome sequences of rice and Brachypodium established co-linearity of the Ml3D232 genomic region with a 1.4 Mb genomic region on Brachypodium distachyon chromosome 4, and a 1.2 Mb contig located on the Oryza sativa chromosome 9. Our comparative approach enabled us to develop new EST-STS markers and to delimit the genomic region carrying Ml3D232 to a 0.8 cM segment that is collinear with a 558 kb region on B. distachyon. Eight EST markers, including an NBS-LRR analog, co-segregated with Ml3D232 to provide a target site for fine genetic mapping, chromosome landing and map-based cloning of the powdery mildew resistance gene. This newly developed common wheat germplasm provides broad-spectrum resistance to powdery mildew and a valuable resource for wheat breeding programs.
小麦白粉病是由禾本科布氏白粉菌引起的,是世界范围内最重要的小麦病害之一,利用多样化的抗病基因进行抗性育种是预防白粉病爆发的最有前途的方法。一个源自以色列收集的野生二粒小麦(Triticum turgidum var. dicoccoides)的白粉病抗性基因,已经通过杂交和回交的方式被转移到六倍体小麦品系 3D232 中。用 21 个禾本科布氏白粉菌小麦专化型接种 3D232 的结果表明,3D232 对所有测试的白粉病分离物均具有抗性。利用 F2 分离群体和 F3 家系对 3D232 进行的遗传分析表明,一个单一的显性基因 Ml3D232 在宿主幼苗期赋予抗性。通过应用分子标记和混池分离分析法(BSA),我们已经确定了多态性简单序列重复(SSR)、表达序列标签(EST)和衍生序列标签位点(STS)标记,以确定 Ml3D232 位于 5BL 染色体 0.59-0.76 -bin 中。利用水稻和短柄草的图谱化 EST 标记和基因组序列进行比较遗传分析,将 Ml3D232 基因组区域与短柄草染色体 4 上的 1.4 Mb 基因组区域以及水稻 9 号染色体上的 1.2 Mb 连续体建立了共线性关系。我们的比较方法使我们能够开发新的 EST-STS 标记,并将携带 Ml3D232 的基因组区域限定在与短柄草的 558 kb 区域共线性的 0.8 cM 片段内。包括一个 NBS-LRR 类似物在内的 8 个 EST 标记与 Ml3D232 共分离,为精细遗传作图、染色体着陆和基于图谱的白粉病抗性基因克隆提供了一个目标位点。这个新开发的普通小麦种质资源为小麦白粉病提供了广谱抗性,是小麦育种计划的宝贵资源。