Department of Evolutionary and Environmental Biology, The Institute of Evolution, Faculty of Science and Science Education, University of Haifa, Mt. Carmel, 31905, Haifa, Israel.
Theor Appl Genet. 2010 Aug;121(3):499-510. doi: 10.1007/s00122-010-1326-5. Epub 2010 Apr 21.
The gene-pool of wild emmer wheat, Triticum turgidum ssp. dicoccoides, harbors a rich allelic repertoire for disease resistance. In the current study, we made use of tetraploid wheat mapping populations derived from a cross between durum wheat (cv. Langdon) and wild emmer (accession G18-16) to identify and map a new powdery mildew resistance gene derived from wild emmer wheat. Initially, the two parental lines were screened with a collection of 42 isolates of Blumeria graminis f. sp. tritici (Bgt) from Israel and 5 isolates from Switzerland. While G18-16 was resistant to 34 isolates, Langdon was resistant only to 5 isolates and susceptible to 42 isolates. Isolate Bgt#15 was selected to differentiate between the disease reactions of the two genotypes. Segregation ratio of F(2-3) and recombinant inbreed line (F(7)) populations to inoculation with isolate Bgt#15 indicated the role of a single dominant gene in conferring resistance to Bgt#15. This gene, temporarily designated PmG16, was located on the distal region of chromosome arm 7AL. Genetic map of PmG16 region was assembled with 32 simple sequence repeat (SSR), sequence tag site (STS), Diversity array technology (DArT) and cleaved amplified polymorphic sequence (CAPS) markers and assigned to the 7AL physical bin map (7AL-16). Using four DNA markers we established colinearity between the genomic region spanning the PmG16 locus within the distal region of chromosome arm 7AL and the genomic regions on rice chromosome 6 and Brachypodium Bd1. A comparative analysis was carried out between PmG16 and other known Pm genes located on chromosome arm 7AL. The identified PmG16 may facilitate the use of wild alleles for improvement of powdery mildew resistance in elite wheat cultivars via marker-assisted selection.
野生二粒小麦(Triticum turgidum ssp. dicoccoides)的基因库蕴藏着丰富的抗病等位基因。在本研究中,我们利用源于硬粒小麦(品种 Langdon)和野生二粒小麦(G18-16 品系)杂交的四倍体小麦作图群体,鉴定并定位了一个来自野生二粒小麦的新的抗白粉病基因。最初,用来自以色列的 42 个小麦白粉菌(Blumeria graminis f. sp. tritici,Bgt)分离物和来自瑞士的 5 个分离物对两个亲本系进行筛选。G18-16 对 34 个分离物具有抗性,而 Langdon 仅对 5 个分离物具有抗性,对 42 个分离物敏感。选择 Bgt#15 分离物来区分两种基因型的发病反应。用 Bgt#15 接种 F(2-3)和重组自交系(F(7))群体的分离比表明,一个单一显性基因在赋予对 Bgt#15 的抗性中起作用。这个基因暂时命名为 PmG16,位于 7AL 染色体臂的远端区域。用 32 个简单重复序列(SSR)、序列标签位点(STS)、多样性阵列技术(DArT)和切割扩增多态性序列(CAPS)标记组装 PmG16 区域的遗传图谱,并将其分配到 7AL 物理 bin 图谱(7AL-16)。利用四个 DNA 标记,我们在 7AL 染色体臂远端的 PmG16 基因座所在的基因组区域和水稻染色体 6 和短柄草 Bd1 上的基因组区域之间建立了共线性。对位于 7AL 染色体臂上的 PmG16 和其他已知 Pm 基因进行了比较分析。鉴定的 PmG16 可能有助于通过标记辅助选择利用野生等位基因改良普通小麦品种的白粉病抗性。