首页> 外文期刊>Journal of Phytopathology >Isolation and Expression of an NBS-LRR Protein-encoding Resistance Gene Candidate that Segregates with a Rust Resistance Gene in Sunflower
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Isolation and Expression of an NBS-LRR Protein-encoding Resistance Gene Candidate that Segregates with a Rust Resistance Gene in Sunflower

机译:NBS-LRR蛋白编码抗性基因候选物的分离和表达与向日葵的抗锈性基因分离

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Sunflower rust caused by Puccinia helianthi is considered to be a major disease of sunflower because it causes significant yield losses. RACE-PCR was used to isolate a full-length cDNA of resistance gene candidate (RGC) 260, which segregated with the R-adv resistance gene conferring resistance to rust. The predicted protein of this RGC is 1340 amino acids long and belongs to the CC-NBS-LRR subfamily of plant resistance genes. To verify that RGC260 belongs to a functional group of resistance genes, the transcript accumulation of the RGC was detected using real-time PCR following infection of plants with P. helianthi and Plasmopara halstedii, the two major pathogens of sunflower. The expression profile of this RGC revealed that its expression was specifically induced during an incompatible interaction between sunflower and P. helianthi. Expression profiles of defense genes and component signaling genes proposed the nature of this pathosystem as a gene-for-gene interaction. These results suggest that RGC260 may play a critical role in protecting sunflower cells against P. helianthi.
机译:由Puccinia helianthi引起的向日葵锈病被认为是向日葵的主要病害,因为它导致大量的产量损失。 RACE-PCR用于分离抗性基因候选基因(RGC)260的全长cDNA,该基因与R-adv抗性基因分离,赋予抗锈性。该RGC的预测蛋白长1340个氨基酸,属于植物抗性基因的CC-NBS-LRR亚家族。为了验证RGC260属于抗性基因的功能组,在植物被向日葵的两个主要病原体P. helianthi和Plasmopara halstedii感染后,使用实时PCR检测了RGC的转录物积累。该RGC的表达概况表明,它的表达是在向日葵和P. helianthi之间不相容相互作用期间特异性诱导的。防御基因和成分信号转导基因的表达谱提出了该病理系统作为基因对基因相互作用的性质。这些结果表明,RGC260可能在保护向日葵细胞免受疟原虫的侵害中起关键作用。

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