Liu D, Xia X -C, He Z -H, Xu S -C
Institute of Crop Science, National Wheat Improvement Center/The National Key Facility for Crop Gene Resources and Genetic Improvement, Chinese Academy of Agricultural Sciences, Beijing, China
Phytopathology. 2008 Dec;98(12):1291-6. doi: 10.1094/PHYTO-98-12-1291.
Stripe rust and powdery mildew, caused by Puccinia striiformis f. sp. tritici and Blumeria graminis f. sp. tritici, respectively, are severe diseases in wheat (Triticum aestivum) worldwide. In our study, differential amplification of a 201-bp cDNA fragment was obtained in a cDNA-amplified fragment length polymorphism (AFLP) analysis between near-isogenic lines Yr10NIL and Avocet S, inoculated with P. striiformis f. sp. tritici race CYR29. A full-length cDNA (1,357 bp) of a homeobox-like gene, TaHLRG (GenBank accession no. EU385606), was obtained in common wheat based on the sequence of GenBank accession AW448633 with high similarity to the above fragment. The genomic DNA sequence (2,396 bp) of TaHLRG contains three exons and two introns. TaHLRG appeared to be a novel homeobox-like gene, encoding a protein with a predicted 66-amino-acid homeobox domain. It was involved in race-specific responses to stripe rust in real-time quantitative polymerase chain reaction (PCR) analyses with Yr9NIL, Yr10NIL, and Avocet S. It was also associated with adult-plant resistance to stripe rust and powdery mildew based on the field trials of doubled haploid lines derived from the cross Bainong 64/Jingshuang 16 and two F(2:3) populations from the crosses Lumai 21/Jingshuang 16 and Strampelli/Huixianhong. A functional marker, THR1 was developed based on the sequence of TaHLRG and located on chromosome 6A using a set of Chinese Spring nulli-tetrasomic lines.
条锈病和白粉病分别由条形柄锈菌小麦专化型(Puccinia striiformis f. sp. tritici)和小麦白粉菌(Blumeria graminis f. sp. tritici)引起,是全球小麦(Triticum aestivum)上的严重病害。在我们的研究中,在用条形柄锈菌小麦专化型小种CYR29接种的近等基因系Yr10NIL和阿伏塞特S(Avocet S)之间进行的cDNA扩增片段长度多态性(AFLP)分析中,获得了一个201 bp cDNA片段的差异扩增。基于与上述片段高度相似的GenBank登录号AW448633的序列,在普通小麦中获得了一个类同源异型盒基因TaHLRG的全长cDNA(1357 bp)(GenBank登录号EU385606)。TaHLRG的基因组DNA序列(2396 bp)包含3个外显子和2个内含子。TaHLRG似乎是一个新的类同源异型盒基因,编码一种具有预测的66个氨基酸的同源异型盒结构域的蛋白质。在对Yr9NIL、Yr10NIL和阿伏塞特S进行的实时定量聚合酶链反应(PCR)分析中,它参与了对条锈病的小种特异性反应。基于百农64/京双16杂交衍生的双单倍体系以及鲁麦21/京双16和斯特拉姆佩利/辉县红杂交的两个F(2:3)群体的田间试验,它还与成株对条锈病和白粉病的抗性相关。基于TaHLRG的序列开发了一个功能标记THR1,并使用一套中国春缺体-四体品系将其定位在6A染色体上。