首页> 外文期刊>Nucleic Acids Research >An NMR and mutational study of the pseudoknot within the gene 32 mRNA of bacteriophage T2: insights into a family of structurally related RNA pseudoknots.
【24h】

An NMR and mutational study of the pseudoknot within the gene 32 mRNA of bacteriophage T2: insights into a family of structurally related RNA pseudoknots.

机译:噬菌体T2基因32 mRNA中假结的NMR和突变研究:洞悉与结构相关的RNA假结家族。

获取原文
获取原文并翻译 | 示例
           

摘要

NMR methods were used to investigate a series of mutants of the pseudoknot within the gene 32 messenger RNA of bacteriophage T2, for the purpose of investigating the range of sequences, stem and loop lengths that can form a similar pseudoknot structure. This information is of particular relevance since the T2 pseudoknot has been considered a representative of a large family of RNA pseudoknots related by a common structural motif, previously referred to as 'common pseudoknot motif 1' or CPK1. In the work presented here, a mutated sequence with the potential to form a pseudoknot with a 6 bp stem2 was shown to adopt a pseudoknot structure similar to that of the wild-type sequence. This result is significant in that it demonstrates that pseudoknots with 6 bp in stem2 and a single nucleotide in loop1 are indeed feasible. Mutated sequences with the potential to form pseudoknots with either 5 or 8 bp in stem2 yielded NMR spectra that could not confirm the formation of a pseudoknot structure. Replacing the adenosine nucleotide in loop1 of the wild-type pseudoknot with any one of G, C or U did not significantly alter the pseudoknot structure. Taken together, the results of this study provide support for the existence of a family of similarly structured pseudoknots with two coaxially stacked stems, either 6 or 7 bp in stem2, and a single nucleotide in loop1. This family includes many of the pseudoknots predicted to occur downstream of the frameshift or readthrough sites in a significant number of viral RNAs.
机译:NMR方法用于研究噬菌体T2基因32信使RNA内的一系列假结突变体,目的是研究可形成相似假结结构的序列范围,茎和环长度。该信息特别相关,因为T2假结已被认为是由共同的结构基序(以前称为“普通假结基序1”或CPK1)相关的一大类RNA假结的代表。在本文介绍的工作中,有潜力与6 bp stem2形成假结的突变序列显示出与野生型序列相似的假结结构。该结果很重要,因为它表明在stem2中具有6 bp的假结和在loop1中具有单个核苷酸的假结确实是可行的。可能在stem2中形成5或8 bp假结的突变序列产生的NMR光谱无法确认假结结构的形成。用G,C或U中的任何一个替换野生型假结的loop1中的腺苷核苷酸都不会显着改变假结的结构。两者合计,这项研究的结果提供了存在的结构相似的假结家族的支持,假结具有两个同轴堆叠的茎,茎2中为6或7 bp,而loop1中为单个核苷酸。这个家族包括许多假结,这些假结预计会出现在大量病毒RNA的移码或通读位点的下游。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号