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首页> 外文期刊>Journal of Molecular Biology >The role of RNA pseudoknot stem 1 length in the promotion of efficient -1 ribosomal frameshifting.
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The role of RNA pseudoknot stem 1 length in the promotion of efficient -1 ribosomal frameshifting.

机译:RNA假结茎1长度在促进有效-1核糖体移码中的作用。

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The ribosomal frameshifting signal present in the genomic RNA of the coronavirus infectious bronchitis virus (IBV) contains a classic hairpin-type RNA pseudoknot that is believed to possess coaxially stacked stems of 11 bp (stem 1) and 6 bp (stem 2). We investigated the influence of stem 1 length on the frameshift process by measuring the frameshift efficiency in vitro of a series of IBV-based pseudoknots whose stem 1 length was varied from 4 to 13 bp in single base-pair increments. Efficient frameshifting depended upon the presence of a minimum of 11 bp; pseudoknots with a shorter stem 1 were either non-functional or had reduced frameshift efficiency, despite the fact that a number of them had a stem 1 with a predicted stability equal to or greater than that of the wild-type IBV pseudoknot. An upper limit for stem 1 length was not determined, but pseudoknots containing a 12 or 13 bp stem 1 were fully functional. Structure probing analysis was carried out on RNAs containing either a ten or 11 bp stem 1; these experiments confirmed that both RNAs formed pseudoknots and appeared to be indistinguishable in conformation. Thus the difference in frameshifting efficiency seen with the two structures was not simply due to an inability of the 10 bp stem 1 construct to fold into a pseudoknot. In an attempt to identify other parameters which could account for the poor functionality of the shorter stem 1-containing pseudoknots, we investigated, in the context of the 10 bp stem 1 construct, the influence on frameshifting of altering the slippery sequence-pseudoknot spacing distance, loop 2 length, and the number of G residues at the bottom of the 5'-arm of stem 1. For each parameter, it was possible to find a condition where a modest stimulation of frameshifting was observable (about twofold, from seven to a maximal 17 %), but we were unable to find a situation where frameshifting approached the levels seen with 11 bp stem 1 constructs (48-57 %). Furthermore, in the next smaller construct (9 bp stem 1), changing the bottom four base-pairs to G.C (the optimal base composition) only stimulated frameshifting from 3 to 6 %, an efficiency about tenfold lower than seen with the 11 bp construct. Thus stem 1 length is a major factor in determining the functionality of this class of pseudoknot and this has implications for models of the frameshift process. Copyright 1999 Academic Press.
机译:冠状病毒感染性支气管炎病毒(IBV)的基因组RNA中存在的核糖体移码信号包含经典的发夹型RNA假结,据信具有11 bp(茎1)和6 bp(茎2)的同轴堆叠茎。我们通过测量一系列基于IBV的假结的移码效率,研究了茎1长度对移码过程的影响,这些假结的茎1长度在单个碱基对的范围内从4到13 bp不等。有效的移码取决于最小11 bp的存在。茎1较短的假结要么没有功能,要么移码效率降低,尽管事实上许多假结的茎1的预测稳定性等于或大于野生型IBV假结。茎1长度的上限尚未确定,但包含12或13 bp茎1的假结完全起作用。对含有10或11 bp茎1的RNA进行结构探测分析;这些实验证实两个RNA均形成假结,并且在构象上似乎无法区分。因此,用这两种结构观察到的移码效率的差异不仅仅是由于10 bp茎1构建体无法折叠成假结而引起的。为了确定其他可能解释较短茎1假结功能差的参数,我们在10 bp茎1构造的背景下研究了滑移序列-伪尾间隔距离对移码的影响,循环2的长度以及茎1的5'臂底部的G残基数。对于每个参数,都可以找到一种条件,在这种条件下可以观察到适度的移码刺激(大约是两倍,从七个到另一个)最大17%),但我们无法找到移码接近11 bp茎1构建体所见水平的情况(48-57%)。此外,在下一个较小的构建体(9 bp茎1)中,将底部的四个碱基对更改为GC(最佳碱基组成)仅会刺激从3%移至6%的移码,效率比使用11 bp的构建体低约十倍。因此,茎1的长度是确定此类伪结功能的主要因素,这对移码过程的模型有影响。版权所有1999,学术出版社。

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