首页> 外文OA文献 >Protein-mediated RNA folding governs sequence-specific interactions between rotavirus genome segments
【2h】

Protein-mediated RNA folding governs sequence-specific interactions between rotavirus genome segments

机译:蛋白质介导的RNa折叠控制轮状病毒基因组区段之间的序列特异性相互作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Segmented RNA viruses are ubiquitous pathogens, which include influenza viruses and rotaviruses. A major challenge in understanding their assembly is the combinatorial problem of a non-random selection of a full genomic set of distinct RNAs. This process involves complex protein/RNA interactions, which are often obscured by non-specific binding at concentrations approaching in vvo assembly conditions. Here, we present direct experimental evidence of sequence-specific inter-segment interactions in rotaviruses, taking place in a complex RNA- and protein- rich milieu. We show that binding of the rotaviral protein NSP2 to ssRNAs results in the remodeling of RNA, which is conducive to formation of inter-segment contacts. To identify the sites of these interactions, we have developed an RNA-RNA SELEX approach for mapping the sequences involved in inter-segment base-pairing. Our findings elucidate the molecular basis underlying inter-segment interactions in rotaviruses, paving the way for delineating RNA-RNA interactions that govern assembly of other segmented RNA viruses
机译:分段的RNA病毒是普遍存在的病原体,包括流感病毒和轮状病毒。理解其组装的主要挑战是非随机选择完整基因组的不同RNA的组合问题。此过程涉及复杂的蛋白质/ RNA相互作用,通常在接近vvo组装条件的浓度下被非特异性结合所掩盖。在这里,我们提供轮状病毒中特定序列间相互作用的直接实验证据,发生在富含RNA和蛋白质的复杂环境中。我们表明,轮状病毒蛋白NSP2与ssRNAs的结合导致RNA的重塑,这有利于段间接触的形成。为了确定这些相互作用的位点,我们开发了一种RNA-RNA SELEX方法来定位涉及段间碱基配对的序列。我们的发现阐明了轮状病毒中片段间相互作用的分子基础,为描述支配其他分段RNA病毒装配的RNA-RNA相互作用铺平了道路。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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