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在天然和修饰的RNA模板的3' 类tRNA结构内,雀麦花叶病毒复制酶引发负链合成。

Minus-strand initiation by brome mosaic virus replicase within the 3' tRNA-like structure of native and modified RNA templates.

作者信息

Miller W A, Bujarski J J, Dreher T W, Hall T C

出版信息

J Mol Biol. 1986 Feb 20;187(4):537-46. doi: 10.1016/0022-2836(86)90332-3.

Abstract

An RNA-dependent RNA polymerase (replicase) extract from brome mosaic virus-infected barley leaves has been shown to initiate synthesis of (-) sense RNA from (+) sense virion RNA. Initiation occurred de novo, as demonstrated by the incorporation of [gamma-32P]GTP into the product. Sequencing using cordycepin triphosphate to terminate (-) strands during their synthesis by the replicase generated sequence ladders that confirmed that copying was accurate, and that initiation occurred very close to the 3' end. The precise site of initiation was further defined by testing the replicase template activity after stepwise removal of 3'-terminal nucleotides. Whereas removal of the terminal A did not decrease template activity, removal of the next nucleotide (C-2) did. Thus, initiation almost certainly occurs opposite the penultimate 3'-nucleotide (C-2) in vitro. The structure of the double-stranded replicative form of RNA isolated from brome mosaic virus-infected leaves was consistent with such a mechanism occurring in vivo, in that it lacked the 3'-terminal A found on virion RNAs. The specific site of (-) strand initiation and normal template activity were retained for RNAs with as many as 15 to 30 A residues added to the 3' end. However, only limited oligonucleotide 3' extensions can be present on active templates. In order to assess the 5' extent of sequences required for an active template, a 134-nucleotide-long fragment of brome mosaic virus RNA, corresponding to the tRNA-like structure, was generated. This RNA had high template activity, but a shorter 3' (85-nucleotide) fragment was inactive. RNAs with various heterologous sequences 5' to position 134 also showed high template activity. Thus, the 3'-terminal tRNA-like structure common to all four brome mosaic virus virion RNAs contains all of the signals required for initiation of replication, and sequences 5' to it do not play a role in template selection.

摘要

已证明,从感染了雀麦花叶病毒的大麦叶片中提取的一种依赖RNA的RNA聚合酶(复制酶)能从(+)义病毒粒子RNA起始合成(-)义RNA。起始是从头开始的,这通过将[γ-32P]GTP掺入产物得以证明。在复制酶合成(-)链过程中,使用三磷酸虫草素终止(-)链进行测序,生成的序列梯证实了复制是准确的,并且起始发生在非常靠近3'端的位置。通过逐步去除3'末端核苷酸后测试复制酶模板活性,进一步确定了起始的精确位点。去除末端A不会降低模板活性,而去除下一个核苷酸(C-2)则会降低。因此,在体外起始几乎肯定发生在倒数第二个3'-核苷酸(C-2)相对的位置。从感染雀麦花叶病毒的叶片中分离出的双链复制型RNA的结构与体内发生的这种机制一致,因为它缺少病毒粒子RNA上存在的3'-末端A。对于在3'端添加了多达15至30个A残基的RNA,(-)链起始的特定位点和正常模板活性得以保留。然而,活性模板上只能存在有限的寡核苷酸3'延伸。为了评估活性模板所需序列的5'范围,生成了一段与类tRNA结构相对应的134个核苷酸长的雀麦花叶病毒RNA片段。该RNA具有高模板活性,但较短的3'(85个核苷酸)片段无活性。在位置134上游具有各种异源序列的RNA也显示出高模板活性。因此,所有四种雀麦花叶病毒粒子RNA共有的3'-末端类tRNA结构包含复制起始所需的所有信号,其上游序列在模板选择中不起作用。

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