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劳氏肉瘤病毒核糖体移码信号的二级结构与突变分析

Secondary structure and mutational analysis of the ribosomal frameshift signal of rous sarcoma virus.

作者信息

Marczinke B, Fisher R, Vidakovic M, Bloys A J, Brierley I

机构信息

Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QP, UK.

出版信息

J Mol Biol. 1998 Nov 27;284(2):205-25. doi: 10.1006/jmbi.1998.2186.

Abstract

Expression of the Gag-Pol polyprotein of Rous sarcoma virus (RSV) requires a -1 ribosomal frameshifting event at the overlap region of the gag and pol open reading frames. The signal for frameshifting is composed of two essential mRNA elements; a slippery sequence (AAAUUUA) where the ribosome changes reading frame, and a stimulatory RNA structure located immediately downstream. This RNA is predicted to be a complex stem-loop but may also form an RNA pseudoknot. We have investigated the structure of the RSV frameshift signal by a combination of enzymatic and chemical structure probing and site-directed mutagenesis. The stimulatory RNA is indeed a complex stem-loop with a long stable stem and two additional stem-loops contained as substructures within the main loop region. The substructures are not however required for frameshifting. Evidence for an additional interaction between a stretch of nucleotides in the main loop and a region downstream to generate an RNA pseudoknot was obtained from an analysis of the frameshifting properties of RSV mutants translated in the rabbit reticulocyte lysate in vitro translation system. Mutations that disrupted the predicted pseudoknot-forming sequences reduced frameshifting but when the mutations were combined and should re-form the pseudoknot, frameshifting was restored to a level approaching that of the wild-type construct. It was also observed that the predicted pseudoknot-forming regions had reduced sensitivity to cleavage by the single-stranded probe imidazole. Overall, however, the structure probing data indicate that the pseudoknot interaction is weak and may form transiently. In comparison to other characterised RNA structures present at viral frameshift signals, the RSV stimulator falls into a novel group. It cannot be considered to be a simple hairpin-loop yet it is distinct from other well characterised frameshift-inducing RNA pseudoknots in that the overall contribution of the RSV pseudoknot to frameshifting is less dramatic.

摘要

劳氏肉瘤病毒(RSV)的Gag-Pol多聚蛋白的表达需要在gag和pol开放阅读框的重叠区域发生-1核糖体移码事件。移码信号由两个必需的mRNA元件组成;一个滑序列(AAAUUUA),核糖体在此处改变阅读框,以及一个位于紧邻下游的刺激性RNA结构。该RNA预计是一个复杂的茎环结构,但也可能形成RNA假结。我们通过酶促和化学结构探测以及定点诱变相结合的方法研究了RSV移码信号的结构。刺激性RNA确实是一个复杂的茎环结构,具有一个长的稳定茎以及两个作为子结构包含在主环区域内的额外茎环。然而,这些子结构对于移码并非必需。通过对在兔网织红细胞裂解物体外翻译系统中翻译的RSV突变体的移码特性进行分析,获得了主环中一段核苷酸与下游区域之间存在额外相互作用以形成RNA假结的证据。破坏预计的假结形成序列的突变会降低移码,但当这些突变组合并应重新形成假结时,移码恢复到接近野生型构建体的水平。还观察到,预计的假结形成区域对单链探针咪唑切割的敏感性降低。然而,总体而言,结构探测数据表明假结相互作用较弱,可能是瞬时形成的。与病毒移码信号处存在的其他已表征的RNA结构相比,RSV刺激物属于一个新的类别。它不能被认为是一个简单的发夹环,但它与其他特征明确的移码诱导RNA假结不同,因为RSV假结对移码的总体贡献较小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f38/7126186/7986ef0d0117/gr1_lrg.jpg

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