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Structural view on recycling of archaeal and eukaryotic ribosomes after canonical termination and ribosome rescue

机译:规范终止和核糖体抢救后古细菌和真核生物核糖体回收的结构性观点

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摘要

Ribosome recycling usually occurs after canonical termination triggered by a stop codon. Additionally, ribosomes that are stalled by aberrant mRNAs need to be recognized and subsequently recycled. In eukaryotes and archaea, the factors involved in canonical termination and ribosome rescue are structurally and functionally related. Both termination and ribosome rescue are mediated by class I release factors (eRF1/aRF1 in eukaryotic/archaeal termination) or their paralogs (Pelota/aPelota for ribosome rescue) and homologs of translational GTPases (eRF3/aEF1α in termination, Hbs1/aEF1α in ribosome rescue). These events are followed by recycling of the ribosome. Recently the ATPase ABCE1 was shown to be the main ribosome recycling factor. In concert with eRF1 or Pelota, ABCE1 dissociates the ribosome into subunits. During the past two years, several structures of ribosome rescue and ribosome recycling complexes have been solved by cryo-electron microscopy and crystallography. These structures along with recent functional data make it possible to propose a molecular model of these late translation events in termination and recycling.
机译:核糖体回收通常在终止密码子触发规范终止后发生。另外,被异常mRNA停滞的核糖体需要被识别并随后被回收。在真核生物和古细菌中,规范终止和核糖体拯救所涉及的因素在结构和功能上均相关。终止和核糖体拯救均由I类释放因子(真核/古细菌终止中的eRF1 / aRF1)或其旁系同源物(核糖体拯救的Pelota / aPelota)和翻译型GTP酶的同源物(终止中的eRF3 /aEF1α,核糖体中的Hbs1 /aEF1α)介导。拯救)。这些事件之后是核糖体的再循环。最近,ATPase ABCE1被证明是主要的核糖体回收因子。与eRF1或Pelota协同作用,ABCE1将核糖体解离成亚基。在过去的两年中,通过冷冻电子显微镜和晶体学已经解决了核糖体拯救和核糖体再循环复合物的几种结构。这些结构以及最新的功能数据使我们有可能提出这些终止和回收中后期翻译事件的分子模型。

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