Napthine S, Liphardt J, Bloys A, Routledge S, Brierley I
Division of Virology Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QP, UK.
J Mol Biol. 1999 May 7;288(3):305-20. doi: 10.1006/jmbi.1999.2688.
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.
传染性支气管炎病毒(IBV)基因组RNA中存在的核糖体移码信号包含一个经典的发夹型RNA假结,据信其具有11个碱基对(茎1)和6个碱基对(茎2)的同轴堆叠茎。我们通过测量一系列基于IBV的假结在体外的移码效率来研究茎1长度对移码过程的影响,这些假结的茎1长度以单碱基对增量从4个碱基对变化到13个碱基对。高效移码依赖于至少11个碱基对的存在;茎1较短的假结要么无功能,要么移码效率降低,尽管其中一些假结的茎1预测稳定性等于或大于野生型IBV假结。未确定茎1长度的上限,但包含12或13个碱基对茎1的假结功能完全正常。对包含10或11个碱基对茎1的RNA进行了结构探测分析;这些实验证实两种RNA都形成了假结,并且在构象上似乎无法区分。因此,两种结构在移码效率上的差异不仅仅是由于10个碱基对茎1构建体无法折叠成假结。为了试图确定其他可以解释较短茎1假结功能不佳的参数,我们在10个碱基对茎1构建体的背景下,研究了改变滑序列 - 假结间隔距离、环2长度以及茎1 5'臂底部G残基数量对移码的影响。对于每个参数,都有可能找到一种情况,其中可以观察到移码有适度的刺激(约两倍,从7%到最大17%),但我们无法找到移码接近11个碱基对茎1构建体所见水平(48 - 57%)的情况。此外,在次小的构建体(9个碱基对茎1)中,将底部四个碱基对变为G.C(最佳碱基组成)仅将移码刺激从3%提高到6%,效率比11个碱基对构建体低约十倍。因此,茎1长度是决定这类假结功能的主要因素,这对移码过程的模型有影响。