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1型人类免疫缺陷病毒RNA的主要5'端对应于G456。

The major 5' end of HIV type 1 RNA corresponds to G456.

作者信息

Menees Thomas M, Müller Barbara, Kräusslich Hans-Georg

机构信息

School of Biological Sciences, Division of Cell Bilogy and Biophysics, University of Missouri-Kansas City, Kansas City, Missouri 64110, USA.

出版信息

AIDS Res Hum Retroviruses. 2007 Aug;23(8):1042-8. doi: 10.1089/aid.2006.0275.

Abstract

In the course of studies on HIV-1 RNA structure, we determined that the main 5' end of viral RNA from virions and virus producer cells corresponds to G456 in the proviral DNA sequence, one or two nucleotides down-stream from the reported ends that correspond to G454 and G455. We mapped 5' ends using the highly accurate RNA ligase-mediated rapid amplification of cDNA ends (RLM-RACE) method. The reactivity of the 5' ends indicates that they are mainly capped, although the presence of some uncapped (5'-triphosphorylated) RNA cannot formally be excluded. When we used a 5' mapping method susceptible to incorporating a cytosine at the 3' end of cDNA first strands, at a position templated by the 7-methylguanosine cap, 50% of clones derived from virion RNA had incorporated the additional cytosine. Reassignment of the 5' end has consequences for the design of short RNAs used to study HIV-1 RNA structural dynamics.

摘要

在对HIV-1 RNA结构的研究过程中,我们确定来自病毒粒子和病毒产生细胞的病毒RNA的主要5'端对应于前病毒DNA序列中的G456,比报道的对应于G454和G455的末端下游一或两个核苷酸。我们使用高度精确的RNA连接酶介导的cDNA末端快速扩增(RLM-RACE)方法绘制5'端图谱。5'端的反应性表明它们主要被加帽,尽管不能完全排除一些未加帽(5'-三磷酸化)RNA的存在。当我们使用一种易于在cDNA第一链的3'端掺入胞嘧啶的5'作图方法时,在由7-甲基鸟苷帽作为模板的位置,来自病毒粒子RNA的50%的克隆掺入了额外的胞嘧啶。5'端的重新定位对用于研究HIV-1 RNA结构动力学的短RNA的设计有影响。

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