Department of Crop and Soil Sciences, University of Georgia, Griffin Campus, Griffin, GA 30223, USA.
Theor Appl Genet. 2013 Apr;126(4):1067-76. doi: 10.1007/s00122-012-2037-x. Epub 2013 Jan 8.
The discovery of several new loci for resistance to Hessian fly was reported here. QHf.uga-6AL, the late HR61 was recognized from wheat cultivar 26R61 on the distal end of 6AL with resistance to both biotypes E and vH13. It is the first gene or QTL found on this particular chromosome. QHf.uga-3DL and QHf.uga-1AL, physically assigned to the deletion bins 3DL2-0.27-0.81 and 1AL1-0.17-0.61, respectively, were detected for resistance to biotype vH13. Both QTL should represent new loci for Hessian fly resistance and the latter was detectable only in the late seedling stage when tolerance was evident. In addition, QHf.uga-6DS-C and QHf.uga-1AS had minor effect and were identified from the susceptible parent AGS 2000 for resistance to biotype E and vH13, respectively. QHf.uga-6DS-C is different from the known gene H13 on 6DS and QHf.uga-1AS is different from H9 gene cluster on 1AS. These loci also might be new components of Hessian fly resistance, although their LOD values were not highly significant. The QTL detections were all conducted on a RIL mapping population of 26R61/AGS 2000 with good genome coverage of molecular markers. The strategy used in the current study will serve as a good starting point for the discovery and mapping of resistance genes including tolerance to the pest and the closely linked markers will certainly be useful in selecting or pyramiding of these loci in breeding programs.
本文报道了几个新的抗黑森瘿蚊(Hessian fly)基因/位点的发现。QHf.uga-6AL 位于小麦品种 26R61 的 6AL 染色体的远端,对 E 型和 vH13 型均具有抗性。这是该特定染色体上发现的第一个基因或 QTL。QHf.uga-3DL 和 QHf.uga-1AL,物理位置分别被分配到 3DL2-0.27-0.81 和 1AL1-0.17-0.61 的缺失-bin 中,对 vH13 型表现出抗性。这两个 QTL 都代表了黑森瘿蚊抗性的新位点,而后者仅在幼苗后期表现出明显的耐性时才能够被检测到。此外,QHf.uga-6DS-C 和 QHf.uga-1AS 分别从小麦品种 AGS 2000 中被鉴定出对 E 型和 vH13 型的抗性,其效应较小。QHf.uga-6DS-C 与已知的 6DS 上的基因 H13 不同,QHf.uga-1AS 与 1AS 上的 H9 基因簇不同。尽管这些基因座的 LOD 值不高,但它们也可能是黑森瘿蚊抗性的新组成部分。这些 QTL 的检测均在 26R61/AGS 2000 的 RIL 作图群体上进行,该群体具有良好的分子标记基因组覆盖度。本研究中使用的策略将为包括对害虫的耐性在内的抗性基因的发现和作图提供良好的起点,并且紧密连锁的标记在这些基因座的选择或聚合方面肯定会有用。