首页> 美国卫生研究院文献>RNA >The NMR structure of the II–III–VI three-way junction from the Neurospora VS ribozyme reveals a critical tertiary interaction and provides new insights into the global ribozyme structure
【2h】

The NMR structure of the II–III–VI three-way junction from the Neurospora VS ribozyme reveals a critical tertiary interaction and provides new insights into the global ribozyme structure

机译:Neurospora VS核酶的II–III–VI三向连接的NMR结构揭示了关键的三级相互作用并提供了对整体核酶结构的新见解

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

As part of an effort to structurally characterize the complete Neurospora VS ribozyme, NMR solution structures of several subdomains have been previously determined, including the internal loops of domains I and VI, the I/V kissing-loop interaction and the III–IV–V junction. Here, we expand this work by determining the NMR structure of a 62-nucleotide RNA (J236) that encompasses the VS ribozyme II–III–VI three-way junction and its adjoining stems. In addition, we localize Mg2+-binding sites within this structure using Mn2+-induced paramagnetic relaxation enhancement. The NMR structure of the J236 RNA displays a family C topology with a compact core stabilized by continuous stacking of stems II and III, a cis WC/WC G•A base pair, two base triples and two Mg2+ ions. Moreover, it reveals a remote tertiary interaction between the adenine bulges of stems II and VI. Additional NMR studies demonstrate that both this bulge–bulge interaction and Mg2+ ions are critical for the stable folding of the II–III–VI junction. The NMR structure of the J236 RNA is consistent with biochemical studies on the complete VS ribozyme, but not with biophysical studies performed with a minimal II–III–VI junction that does not contain the II–VI bulge–bulge interaction. Together with previous NMR studies, our findings provide important new insights into the three-dimensional architecture of this unique ribozyme.
机译:为了对完整的Neurospora VS核酶进行结构表征,在此之前,已经确定了多个子域的NMR溶液结构,包括域I和VI的内部环,I / V接吻环相互作用和III–IV–V交界处。在这里,我们通过确定包含VS核酶II–III–VI三向连接及其相邻茎的62个核苷酸的RNA(J236)的NMR结构来扩展这项工作。此外,我们利用Mn 2 + 诱导的顺磁弛豫增强在该结构中定位Mg 2 + 结合位点。 J236 RNA的NMR结构显示出C族拓扑结构,其核心紧密,通过连续堆叠茎II和III,顺式WC / WC G•A碱基对,两个碱基三元组和两个Mg 2 + sup>离子。此外,它揭示了茎II和茎VI的腺嘌呤凸起之间的远程三级相互作用。额外的NMR研究表明,这种凸起-凸起相互作用和Mg 2 + 离子对于II-III-VI连接的稳定折叠都是至关重要的。 J236 RNA的NMR结构与完整VS核酶的生物化学研究一致,但与不包含II-VI凸起-凸起相互作用的最小II-III-VI连接进行的生物物理研究不一致。与以前的NMR研究一起,我们的发现为这种独特的核酶的三维结构提供了重要的新见解。

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