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卫星烟草花叶病毒基因组 RNA 的体外二级结构。

In vitro secondary structure of the genomic RNA of satellite tobacco mosaic virus.

机构信息

School of Biology, Georgia Institute of Technology, Atlanta, Georgia, USA.

出版信息

PLoS One. 2013;8(1):e54384. doi: 10.1371/journal.pone.0054384. Epub 2013 Jan 22.

Abstract

Satellite tobacco mosaic virus (STMV) is a T = 1 icosahedral virus with a single-stranded RNA genome. It is widely accepted that the RNA genome plays an important structural role during assembly of the STMV virion. While the encapsidated form of the RNA has been extensively studied, less is known about the structure of the free RNA, aside from a purported tRNA-like structure at the 3' end. Here we use selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) analysis to examine the secondary structure of in vitro transcribed STMV RNA. The predicted secondary structure is unusual in the sense that it is highly extended, which could be significant for protecting the RNA from degradation. The SHAPE data are also consistent with the previously predicted tRNA-like fold at the 3' end of the molecule, which is also known to hinder degradation. Our data are not consistent with the secondary structure proposed for the encapsidated RNA by Schroeder et al., suggesting that, if the Schroeder structure is correct, either the RNA is packaged as it emerges from the replication complex, or the RNA undergoes extensive refolding upon encapsidation. We also consider the alternative, i.e., that the structure of the encapsidated STMV RNA might be the same as the in vitro structure presented here, and we examine how this structure might be organized in the virus. This possibility is not rigorously ruled out by the available data, so it remains open to examination by experiment.

摘要

卫星烟草花叶病毒(STMV)是一种 T = 1 二十面体病毒,具有单链 RNA 基因组。人们普遍认为,在 STMV 病毒粒子的组装过程中,RNA 基因组发挥着重要的结构作用。尽管已对包裹的 RNA 进行了广泛研究,但除了在 3' 端假定的 tRNA 样结构外,对游离 RNA 的结构知之甚少。在这里,我们使用选择性 2'-羟乙酰化分析引物延伸(SHAPE)分析来研究体外转录的 STMV RNA 的二级结构。预测的二级结构非常伸展,这在保护 RNA 免受降解方面可能很重要。SHAPE 数据也与分子 3' 端先前预测的 tRNA 样折叠一致,这也已知会阻碍降解。我们的数据与 Schroeder 等人提出的包裹 RNA 的二级结构不一致,表明如果 Schroeder 结构是正确的,那么 RNA 要么在从复制复合物中出现时就被包裹,要么在包裹时经历广泛的重折叠。我们还考虑了另一种可能性,即包裹的 STMV RNA 的结构可能与这里呈现的体外结构相同,我们研究了这种结构如何在病毒中组织。由于现有数据没有严格排除这种可能性,因此仍然可以通过实验进行检查。

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