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Barley disease resistance gene analogs of the NBS-LRR class: identification and mapping

机译:NBS-LRR类的大麦抗病基因类似物:鉴定和作图

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The majority of verified plant disease resistance genes isolated to date are of the NBS-LRR class, encoding proteins with a predicted nucleotide binding site (NBS) and a leucine-rich repeat (LRR) region. We took advantage of the sequence conservation in the NBS motif to clone, by PCR, gene fragments from barley representing putative disease resistance genes of this class. Over 30 different resistance gene analogs (RGAs) were isolated from the barley cultivar Regatta. These were grouped into 13 classes based on DNA sequence similarity. Actively transcribed genes were identified from all classes but one, and cDNA clones were isolated to derive the complete NBS-LRR protein sequences. Some of the NBS-LRR genes exhibited variation with respect to whether and where particular introns were spliced, as well as frequent premature polyadenylation. DNA sequences related to the majority of the barley RGAs were identified in the recently expanded public rice genomic sequence database, indicating that the rice sequence can be used to extract a large proportion of the RGAs from barley and other cereals. Using a combination of RFLP and PCR marker technique, representatives of all barley RGA gene classes were mapped in the barley genome, to all chromosomes except 4H. A number of the RGA loci map in the vicinity of known disease resistance loci, and the association between RGA S-120 and the nematode resistance locus Ha2on chromosome 2H was further tested by co-segregation analysis. Most of the RGA sequences reported here have not been described previously, and represent a useful resource as candidates or molecular markers for disease resistance genes in barley and other cereals.
机译:迄今为止,大多数已验证的植物抗病性基因均属于NBS-LRR类,编码具有预测核苷酸结合位点(NBS)和富含亮氨酸的重复(LRR)区的蛋白质。我们利用NBS基序中的序列保守性,通过PCR从大麦中克隆了代表此类推定抗病基因的基因片段。从大麦栽培品种Regatta分离出30多种不同的抗性基因类似物(RGA)。基于DNA序列相似性将它们分为13类。从所有类别中鉴定出活跃转录的基因,但只有一种,并分离cDNA克隆以得到完整的NBS-LRR蛋白序列。一些NBS-LRR基因在是否剪接特定内含子和剪接特定内含子方面表现出变异,并且频繁发生过早的聚腺苷酸化。在最近扩展的公共水稻基因组序列数据库中鉴定了与大多数大麦RGA相关的DNA序列,表明该水稻序列可用于从大麦和其他谷物中提取大部分RGA。使用RFLP和PCR标记技术的组合,所有大麦RGA基因类别的代表都在大麦基因组中定位到了4H以外的所有染色体。通过共分离分析进一步检测了已知疾病抗性基因座附近的许多RGA基因座图谱,以及RGAS-120和2H染色体上线虫抗性基因座Ha2之间的关联。这里报道的大多数RGA序列以前没有描述过,它们代表了有用的资源,作为大麦和其他谷物中抗病基因的候选者或分子标记。

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