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首页> 外文期刊>Potato Research >Development of molecular tools for distinguishing between the highly similar Rx1 and Rx2 PVX extreme resistance genes in tetraploid potato.
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Development of molecular tools for distinguishing between the highly similar Rx1 and Rx2 PVX extreme resistance genes in tetraploid potato.

机译:开发用于区分四倍体马铃薯中高度相似的Rx1和Rx2 PVX极端抗性基因的分子工具。

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摘要

The Rx1 and Rx2 are extreme resistance genes, which have been introgressed from different species into potato cultivars and breeding lines. These two genes have a 98% and 96% sequence similarity at the nucleotide as well as at the amino acid level, respectively. Except one extra amino acid in the Rx2 gene, the high variations of the amino acid chain are due to single and double nucleotide variations, which are scattered throughout the coding regions. The high level of sequence similarity makes it complicated to identify these genes and to distinguish them from other highly similar genes, like the Gpa2 or from paralogous sequences by a single polymerase chain reaction (PCR). Here, we report the development of markers for the simple and rapid identification of the Rx1 as well as the Rx2 gene. Further, a multiplex PCR reaction is recommended for the simultaneous detection of both genes in a single reaction. Since these genes reside on different chromosomes, following their inheritance by the multiplex PCR method could help the easy incorporation of both genes into breeding lines. The detection method shown here could be routinely used in marker-assisted selection for Potato virus X extreme resistance and could enhance the effectiveness of potato breeding programs. Besides potato breeding, this method could also be effectively applied to mapping experiments as well as in research studies of resistance.
机译:Rx1和Rx2是极端抗性基因,已从不同物种渗入马铃薯品种和育种系。这两个基因分别在核苷酸和氨基酸水平上具有98%和96%的序列相似性。 Rx2基因中除了一个额外的氨基酸外,氨基酸链的高度变异是由于单核苷酸和双核苷酸变异所致,它们分散在整个编码区中。高度的序列相似性使鉴定这些基因并使它们与其他高度相似的基因(如Gpa2)或通过单聚合酶链反应(PCR)与旁系同源序列区分开来变得很复杂。在这里,我们报告了用于Rx1以及Rx2基因的简单,快速鉴定的标记物的发展。此外,建议在一次反应中同时检测两个基因的多重PCR反应。由于这些基因位于不同的染色体上,因此通过多重PCR方法遗传后,可以帮助将这两个基因轻松整合到育种系中。此处显示的检测方法可以常规用于马铃薯X病毒极端抗性的标记辅助选择,并可以提高马铃薯育种程序的有效性。除马铃薯育种外,该方法还可有效地用于作图实验以及抗性研究。

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