首页> 外文期刊>Nucleic Acids Research >RNA processing machineries in Archaea: the 5 '-3 ' exoribonuclease aRNase J of the beta-CASP family is engaged specifically with the helicase ASH-Ski2 and the 3 '-5 ' exoribonucleolytic RNA exosome machinery
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RNA processing machineries in Archaea: the 5 '-3 ' exoribonuclease aRNase J of the beta-CASP family is engaged specifically with the helicase ASH-Ski2 and the 3 '-5 ' exoribonucleolytic RNA exosome machinery

机译:Archaea中的RNA加工机械:Beta-Casp系列的5'-3'Exoribonuclease Arnase J是专门用氦胺 - Ski2和3'-5'外核典的RNA外容机械进行啮合

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摘要

A network of RNA helicases, endoribonucleases and exoribonucleases regulates the quantity and quality of cellular RNAs. To date, mechanistic studies focussed on bacterial and eukaryal systems due to the challenge of identifying the main drivers of RNA decay and processing in Archaea. Here, our data support that aRNase J, a 5'-3' exoribonuclease of the beta-CASP family conserved in Euryarchaeota, engages specifically with a Ski2-like helicase and the RNA exosome to potentially exert control over RNA surveillance, at the vicinity of the ribosome. Proteomic landscapes and direct protein-protein interaction analyses, strengthened by comprehensive phylogenomic studies demonstrated that aRNase J interplay with ASH-Ski2 and a cap exosome subunit. Finally, Thermococcus barophilus whole-cell extract fractionation experiments provide evidences that an aRNase J/ASH-Ski2 complex might exist in vivo and hint at an association of aRNase J with the ribosome that is emphasised in absence of ASH-Ski2. Whilst aRNase J homologues are found among bacteria, the RNA exosome and the Ski2-like RNA helicase have eukaryotic homologues, underlining the mosaic aspect of archaeal RNA machines. Altogether, these results suggest a fundamental role of beta-CASP RNase/helicase complex in archaeal RNA metabolism.
机译:的RNA解旋酶,内切核糖核酸酶和核糖核酸外切酶的网络调节量和细胞RNA的质量。迄今为止,机理研究集中在细菌和eukaryal系统由于识别RNA降解的主要驱动因素和古菌处理的挑战。这里,我们的数据支持,aRNaseĴ,在广古菌门保守的βCASP家族的5'-3' 核糖核酸外切酶,特别是与接合Ski2状旋酶和RNA外来体超过RNA监视潜在施加控制,在附近核糖体。蛋白质组学风景和直接蛋白质 - 蛋白质相互作用的分析,通过综合phylogenomic加强研究表明,aRNaseĴ相互作用与ASH-Ski2和盖外来体亚基。最后,嗜热barophilus全细胞萃取物分馏实验提供了证据表明一个aRNase焦耳/ ASH-Ski2复杂可能存在于体内和暗示在aRNase的J与在不存在ASH-Ski2的强调核糖体的关联。虽然aRNaseĴ同源物的细菌中找到,外来体RNA和Ski2样RNA解旋酶具有真核同源物,下划线古细菌RNA机器的镶嵌方面。总之,这些结果表明β-内CASP RNA酶的基础性作用/解旋酶在古RNA代谢复杂。

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  • 来源
    《Nucleic Acids Research》 |2020年第7期|共16页
  • 作者单位

    Univ Toulouse Univ Paul Sabatier CBI Lab Microbiol &

    Genet Mol UMR5100 CNRS F-31062 Toulouse France;

    Univ Toulouse Univ Paul Sabatier CBI Lab Microbiol &

    Genet Mol UMR5100 CNRS F-31062 Toulouse France;

    Univ Toulouse Univ Paul Sabatier CBI Lab Microbiol &

    Genet Mol UMR5100 CNRS F-31062 Toulouse France;

    Univ Toulouse Univ Paul Sabatier CBI Lab Microbiol &

    Genet Mol UMR5100 CNRS F-31062 Toulouse France;

    Univ Brest Lab Microbiol Environnements Extremes CNRS IFREMER F-29280 Plouzane France;

    Univ Brest Lab Microbiol Environnements Extremes CNRS IFREMER F-29280 Plouzane France;

    Univ Paris Saclay Micalis Inst AgroParisTech INRA PAPPSO F-78350 Jouy En Josas France;

    Univ Toulouse Univ Paul Sabatier CBI Lab Microbiol &

    Genet Mol UMR5100 CNRS F-31062 Toulouse France;

    Univ Brest Lab Microbiol Environnements Extremes CNRS IFREMER F-29280 Plouzane France;

    Univ Toulouse Univ Paul Sabatier CBI Lab Microbiol &

    Genet Mol UMR5100 CNRS F-31062 Toulouse France;

    Univ Toulouse Univ Paul Sabatier CBI Lab Microbiol &

    Genet Mol UMR5100 CNRS F-31062 Toulouse France;

    Univ Brest Lab Microbiol Environnements Extremes CNRS IFREMER F-29280 Plouzane France;

    Univ Toulouse Univ Paul Sabatier CBI Lab Microbiol &

    Genet Mol UMR5100 CNRS F-31062 Toulouse France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
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