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一种非编码植物病原体可引起番茄的转录和转录后改变。

A noncoding plant pathogen provokes both transcriptional and posttranscriptional alterations in tomato.

机构信息

Instituto de Biología Molecular y Celular de Plantas, Universitat Politècnica de València (UPV), Consejo Superior de Investigaciones Científicas (CSIC), Valencia, Spain.

出版信息

Proteomics. 2013 Mar;13(5):833-44. doi: 10.1002/pmic.201200286. Epub 2013 Jan 31.

Abstract

Viroids are single-stranded, circular, noncoding RNAs that infect plants, causing devastating diseases. In this work, we employed 2D DIGE, followed by MS identification, to analyze the response of tomato plants infected by Citrus exocortis viroid (CEVd). Among the differentially expressed proteins detected, 45 were successfully identified and classified into different functional categories. Validation results by RT-PCR allowed us to classify the proteins into two expression groups. First group included genes with changes at the transcriptional level upon CEVd infection, such as an endochitinase, a β-glucanase, and pathogenesis-related proteins, PR10 and P69G. All these defense proteins were also induced by gentisic acid, a pathogen-induced signal in compatible interactions. The second group of proteins showed no changes at the transcriptional level and included several ribosomal proteins and translation factors, such as the elongation factors 1 and 2 and the translation initiation factor 5-alpha. These results were validated by 2D Western blot, and possible PTMs caused by CEVd infection were detected. Moreover, an interaction between eukaryotic elongation factor 1 and CEVd was observed by 2D Northwestern. The present study provides new protein-related information on the mechanisms of plant resistance to pathogens.

摘要

类病毒是侵染植物的单链环状非编码 RNA,会导致严重的疾病。在这项工作中,我们采用 2D DIGE 和 MS 鉴定分析了受柑橘外束果胶菌 viroid(CEVd)感染的番茄植株的反应。在检测到的差异表达蛋白中,成功鉴定出 45 种,并将其分类到不同的功能类别中。通过 RT-PCR 进行的验证结果使我们能够将这些蛋白分为两组表达类型。第一组包括在 CEVd 感染时转录水平发生变化的基因,如几丁质酶、β-葡聚糖酶和与发病相关的蛋白 PR10 和 P69G。所有这些防御蛋白也被植物病原体诱导的信号物质水杨酸诱导。第二组蛋白在转录水平上没有变化,包括几个核糖体蛋白和翻译因子,如延伸因子 1 和 2 以及翻译起始因子 5-α。这些结果通过 2D Western blot 进行了验证,并检测到了 CEVd 感染引起的可能的翻译后修饰。此外,还通过 2D 西北印迹观察到真核延伸因子 1 和 CEVd 之间的相互作用。本研究为植物对病原体的抗性机制提供了新的蛋白质相关信息。

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