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PK-profiling method for identifying the expression of resistance-associated genes in partially resistant oats to crown rust

机译:PK-Profiling方法,用于鉴定抗性相关基因在部分抗性燕麦中的抗性相关基因的表达

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Protein kinases play a key role in plant cell homeostasis and the activation of defense mechanisms. Partial resistance to fungi in plants is interesting because of its durability. However, the variable number of minor loci associated with this type of resistance hampers the reliable identification of the full range of genes involved. The present work reports the technique of protein kinase (PK)-profiling for the identification of the PK genes induced in the partially resistant oats line MN841801–1 following exposure to the fungus Puccinia coronata. This is the first time this technique has been used with cDNA (complementary DNA) from a suppression subtractive hybridization library obtained after the hybridization of cDNAs from inoculated and mock-inoculated plants. Six degenerate primers based on the conserved domains of protein kinases were used in a PK-profiling assay including cDNA from mock-inoculated leaves and subtracted cDNA. Of the 75.7% of sequences cloned and sequenced that showed significant similarity to resistance genes, 76% were found to code for PKs. Translation and ClustalW2 alignment of each sequence cloned with the complete sequences of the most similar B. distachyon PKs allowed those of the partially resistant oat line to be deduced and characterized. Further, a phylogenetic study carried out after alignment of these B. distachyon PK sequences with the most similar protein sequences of related species also allowed to deduce different functions for the PK cloned. RT-qPCR (Reverse Transcription-quantitative PCR) was analyzed on nine representative sequences to validate the reliability of the employed PK-profiling method as a tool for identifying the expression of resistance-associated genes. PK-profiling would appear to be a useful tool for the identification of the PKs expressed in oats after challenge by P. coronata, and perhaps other pathogens. Most of the PKs studied are related to receptor-like protein kinases expressed shortly after infection. This is in agreement with previous studies indicating a close relationship between partial resistance and the first layer of defense against pathogen used by plants.
机译:蛋白激酶在植物细胞稳态和防御机制的激活中起着关键作用。由于其耐用性,植物中的抗性对真菌的抗性是有趣的。然而,与这种类型的电阻相关的可变数量的次要基因座妨碍了所涉及的全系列基因的可靠鉴定。本作者报告了蛋白激酶(PK)-Profiming的技术,用于鉴定在暴露于真菌普昔逊核苷酸后,鉴定在部分抗性燕麦线MN841801-1中诱导的PK基因。这是第一次通过从接种和模拟接种植物杂交后获得的抑制减法杂交文库的CDNA(互补DNA)。基于蛋白激酶的保守结构域的六个简并引物用于PK - 分析测定法,包括来自嘲弄接种叶片的cDNA和减去cDNA。在克隆和测序的75.7%的序列中显示出与抗性基因的显着相似性,76%被发现为PKS编码。随着最相似B的完整序列克隆的平移和Clustalw2对准每种序列克隆的完整序列。Distachyon PKS允许推导和表征部分耐燕麦线。此外,在对准这些B.Tistachyon PK序列之后进行的系统发育研究,其具有最相似的相关物种的蛋白质序列也使得对PK克隆的不同功能推导出来。分析RT-QPCR(逆转录定量PCR)在九个代表性序列上分析,以验证所用的PK-Profing方法作为用于鉴定抗性相关基因表达的工具的可靠性。 PK-Profiling似乎是鉴定燕麦菌在核心睾丸挑战后鉴定燕麦的PKS的有用工具,也许是其他病原体。所研究的大多数PKS与感染后不久表达的受体样蛋白激酶有关。这与先前的研究一致,表明部分抗性与植物使用的病原体的第一层防御之间的密切关系。

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