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细菌表达的双链 RNA 可保护玉米免受 SCMV 感染。

Bacterially expressed dsRNA protects maize against SCMV infection.

机构信息

Anhui Province Key Laboratory of Crop Biology, School of Life Science, Anhui Agricultural University, Hefei, 230036, China.

出版信息

Plant Cell Rep. 2010 Nov;29(11):1261-8. doi: 10.1007/s00299-010-0911-z. Epub 2010 Aug 24.

Abstract

RNA interference (RNAi) is a sequence-specific, posttranscriptional gene silencing (PTGS) process in plants that is mediated by dsRNA homologous to the silenced gene(s). In this study, we report an efficient method to produce dsRNA using a bacterial expression system. Two fragments of the Sugarcane Mosaic Virus (SCMV) CP (coat protein) gene were amplified by RT-PCR, and cloned into the inverted-repeat cloning vector pUCCRNAi. The two recombinant plasmids were transformed individually into E. coli HT115, an RNase-III deficient strain, and dsRNA was induced by isopropyl-β-D: -thiogalactopyranoside (IPTG). The crude extracts of E. coli HT115 containing large amounts of dsRNA were applied to plants as a spray and the experiment confirmed a preventative efficacy. Our findings demonstrated that spraying crude dsRNA-containing extracts inhibited SCMV infection, and the dsRNA derived from an upstream region (CP1) was more effective than was dsRNA derived from a downstream region (CP2) of the SCMV CP gene. The results provide a valuable tool for plant viral control using dsRNA and the PTGS approach.

摘要

RNA 干扰 (RNAi) 是一种在植物中由 dsRNA 介导的序列特异性转录后基因沉默 (PTGS) 过程,该 dsRNA 与被沉默的基因同源。在本研究中,我们报告了一种使用细菌表达系统产生 dsRNA 的有效方法。通过 RT-PCR 扩增了甘蔗花叶病毒 (SCMV) CP(外壳蛋白)基因的两个片段,并将其克隆到反向重复克隆载体 pUCCRNAi 中。将两个重组质粒分别转化到 RNase-III 缺陷型大肠杆菌 HT115 中,并通过异丙基-β-D: -硫代半乳糖吡喃糖苷 (IPTG) 诱导 dsRNA 的产生。含有大量 dsRNA 的大肠杆菌 HT115 的粗提取物被用作喷雾施用于植物,实验证实了其预防功效。我们的发现表明,喷洒含有 dsRNA 的粗提取物可以抑制 SCMV 感染,并且源自 SCMV CP 基因上游区域 (CP1) 的 dsRNA 比源自下游区域 (CP2) 的 dsRNA 更有效。该结果为使用 dsRNA 和 PTGS 方法进行植物病毒控制提供了有价值的工具。

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