Wiersma Andrew T, Pulman Jane A, Brown Linda K, Cowger Christina, Olson Eric L
Department of Plant, Soil and Microbial Sciences, Michigan State University, 1066 Bogue Street, Room A286, East Lansing, MI, 48824, USA.
Department of Plant Biology and Center for Genomics-Enabled Plant Science, Michigan State University, 612 Wilson Rd, Room 166, East Lansing, MI, 48824, USA.
Theor Appl Genet. 2017 Jun;130(6):1123-1133. doi: 10.1007/s00122-017-2874-8. Epub 2017 Mar 3.
A novel powdery mildew-resistance gene, designated Pm58, was introgressed directly from Aegilops tauschii to hexaploid wheat, mapped to chromosome 2DS, and confirmed to be effective under field conditions. Selectable KASP™ markers were developed for MAS. Powdery mildew caused by Blumeria graminis (DC.) f. sp. tritici (Bgt) remains a significant threat to wheat (Triticum aestivum L.) production. The rapid breakdown of race-specific resistance to Bgt reinforces the need to identify novel sources of resistance. The D-genome species, Aegilops tauschii, is an excellent source of disease resistance that is transferrable to T. aestivum. The powdery mildew-resistant Ae. tauschii accession TA1662 (2n = 2x = DD) was crossed directly with the susceptible hard white wheat line KS05HW14 (2n = 6x = AABBDD) followed by backcrossing to develop a population of 96 BCF introgression lines (ILs). Genotyping-by-sequencing was used to develop a genome-wide genetic map that was anchored to the Ae. tauschii reference genome. A detached-leaf Bgt assay was used to screen BCF ILs, and resistance was found to segregate as a single locus (χ = 2.0, P value = 0.157). The resistance gene, referred to as Pm58, mapped to chromosome 2DS. Pm58 was evaluated under field conditions in replicated trials in 2015 and 2016. In both years, a single QTL spanning the Pm58 locus was identified that reduced powdery mildew severity and explained 21% of field variation (P value < 0.01). KASP™ assays were developed from closely linked GBS-SNP markers, a refined genetic map was developed, and four markers that cosegregate with Pm58 were identified. This novel source of powdery mildew-resistance and closely linked genetic markers will support efforts to develop wheat varieties with powdery mildew resistance.
一个新的抗白粉病基因,命名为Pm58,直接从节节麦渗入到六倍体小麦中,定位在2DS染色体上,并证实在田间条件下有效。开发了可选择的KASP™标记用于分子辅助选择(MAS)。由禾本科布氏白粉菌(DC.)小麦专化型(Bgt)引起的白粉病仍然是小麦(普通小麦)生产的重大威胁。对Bgt的小种专化抗性的快速丧失强化了鉴定新抗性来源的必要性。D基因组物种节节麦是可转移到普通小麦的优良抗病源。将抗白粉病的节节麦种质TA1662(2n = 2x = DD)与感病的硬白小麦品系KS05HW14(2n = 6x = AABBDD)直接杂交,随后回交,构建了一个由96个回交导入系(ILs)组成的群体。通过测序进行基因分型,构建了一个全基因组遗传图谱,并将其锚定到节节麦参考基因组上。采用离体叶片Bgt检测法对回交导入系进行筛选,发现抗性分离为单一位点(χ = 2.0,P值 = 0.157)。该抗性基因命名为Pm58,定位在2DS染色体上。2015年和2016年在田间重复试验中对Pm58进行了评估。在这两年中,均鉴定出一个跨越Pm58位点的单数量性状基因座(QTL),该QTL降低了白粉病严重程度,并解释了21%的田间变异(P值 < 0.01)。基于紧密连锁的简化基因组测序(GBS)-单核苷酸多态性(SNP)标记开发了KASP™检测方法,构建了精细的遗传图谱,并鉴定出四个与Pm58共分离的标记。这个新的抗白粉病来源和紧密连锁的遗传标记将有助于培育抗白粉病小麦品种。