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利用病毒来源的小干扰 RNA 的深度测序重新探讨植物编码的 RNA 依赖性 RNA 聚合酶的抗病毒作用。

Antiviral role of plant-encoded RNA-dependent RNA polymerases revisited with deep sequencing of small interfering RNAs of virus origin.

机构信息

Department of Plant Pathology, Ohio Agricultural Research and Development Center, The Ohio State University, Wooster, OH 44691, USA.

出版信息

Mol Plant Microbe Interact. 2010 Oct;23(10):1248-52. doi: 10.1094/MPMI-06-10-0124.

Abstract

Several recent studies profiled virus-specific small interfering RNAs (vsRNAs) using next generation sequencing platforms and compellingly implicated plant-encoded RNA-dependent RNA polymerases (RDR) in vsRNA biogenesis and vsRNA-mediated antiviral defense. Specifically, both RDR1 and RDR6 were found to contribute to the accumulation of vsRNAs in virus-infected cells. While RDR1 was responsible for the majority of vsRNAs in plants infected with three different viruses, RDR6 acted as a surrogate when RDR1 function was disrupted. Mechanistically, vsRNAs associated with RDR1 mostly mapped to viral RNA regions close to the 5' ends, whereas those associated with RDR6 mapped to more 3' regions and appeared to be dependent on higher viral RNA concentrations. Knocking out both RDR1 and RDR6 led to drastically diminished vsRNA levels concomitant with enhanced viral RNA accumulation. In conclusion, these studies established that RDR1 and RDR6 function synergistically to contain RNA virus infections through the RNA silencing-based antiviral defense.

摘要

几项最近的研究使用下一代测序平台对病毒特异性小干扰 RNA(vsRNA)进行了描绘,并令人信服地表明植物编码的 RNA 依赖性 RNA 聚合酶(RDR)在 vsRNA 生物发生和 vsRNA 介导的抗病毒防御中发挥作用。具体来说,发现 RDR1 和 RDR6 都有助于病毒感染细胞中 vsRNA 的积累。虽然 RDR1 负责感染三种不同病毒的植物中大多数 vsRNA,但当 RDR1 功能被破坏时,RDR6 充当替代物。在机制上,与 RDR1 相关的 vsRNA 主要映射到病毒 RNA 区域靠近 5' 端,而与 RDR6 相关的 vsRNA 映射到更多 3' 区域,并且似乎依赖于更高的病毒 RNA 浓度。敲除 RDR1 和 RDR6 会导致 vsRNA 水平急剧降低,同时病毒 RNA 积累增强。总之,这些研究确立了 RDR1 和 RDR6 通过基于 RNA 沉默的抗病毒防御协同作用来控制 RNA 病毒感染。

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