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Visualization of chemical modifications in the human 80S ribosome structure

机译:可视化人类80S核糖体结构中的化学修饰

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摘要

Chemical modifications of human ribosomal RNA (rRNA) are introduced during biogenesis and have been implicated in the dysregulation of protein synthesis, as is found in cancer and other diseases. However, their role in this phenomenon is unknown. Here we visualize more than 130 individual rRNA modifications in the three-dimensional structure of the human ribosome, explaining their structural and functional roles. In addition to a small number of universally conserved sites, we identify many eukaryote-or human-specific modifications and unique sites that form an extended shell in comparison to bacterial ribosomes, and which stabilize the RNA. Several of the modifications are associated with the binding sites of three ribosome-targeting antibiotics, or are associated with degenerate states in cancer, such as keto alkylations on nucleotide bases reminiscent of specialized ribosomes. This high-resolution structure of the human 80S ribosome paves the way towards understanding the role of epigenetic rRNA modifications in human diseases and suggests new possibilities for designing selective inhibitors and therapeutic drugs.
机译:人核糖体RNA(rRNA)的化学修饰是在生物发生过程中引入的,并且已被证明与蛋白质合成失调有关,如在癌症和其他疾病中所发现的。但是,它们在这种现象中的作用尚不清楚。在这里,我们在人类核糖体的三维结构中可视化了130多个单独的rRNA修饰,解释了它们的结构和功能作用。除了少数普遍保守的位点之外,我们还鉴定了许多真核生物或人特异性修饰和独特位点,与细菌核糖体相比,这些位点形成了延伸的外壳,并且稳定了RNA。几种修饰与三种靶向核糖体的抗生素的结合位点相关,或与癌症的简并状态有关,例如使核苷酸碱基上的酮烷基化使人想起专门的核糖体。人类80S核糖体的这种高分辨率结构为理解表观遗传rRNA修饰在人类疾病中的作用铺平了道路,并为设计选择性抑制剂和治疗药物提供了新的可能性。

著录项

  • 来源
    《Nature 》 |2017年第7681期| 472-477| 共6页
  • 作者单位

    Univ Strasbourg, CNRS, INSERM,IGBMC, Ctr Integrat Biol CBI,Dept Integrated Struct Biol, 1 Rue Laurent Fries, F-67404 Illkirch Graffenstaden, France|Inst Genet & Mol & Cellular Biol IGBMC, 1 Rue Laurent Fries, Illkirch Graffenstaden, France|CNRS, UMR 7104, Illkirch Graffenstaden, France|INSERM, U964, Illkirch Graffenstaden, France|Univ Strasbourg, Illkirch Graffenstaden, France;

    Univ Strasbourg, CNRS, INSERM,IGBMC, Ctr Integrat Biol CBI,Dept Integrated Struct Biol, 1 Rue Laurent Fries, F-67404 Illkirch Graffenstaden, France|Inst Genet & Mol & Cellular Biol IGBMC, 1 Rue Laurent Fries, Illkirch Graffenstaden, France|CNRS, UMR 7104, Illkirch Graffenstaden, France|INSERM, U964, Illkirch Graffenstaden, France|Univ Strasbourg, Illkirch Graffenstaden, France;

    Univ Strasbourg, CNRS, INSERM,IGBMC, Ctr Integrat Biol CBI,Dept Integrated Struct Biol, 1 Rue Laurent Fries, F-67404 Illkirch Graffenstaden, France|Inst Genet & Mol & Cellular Biol IGBMC, 1 Rue Laurent Fries, Illkirch Graffenstaden, France|CNRS, UMR 7104, Illkirch Graffenstaden, France|INSERM, U964, Illkirch Graffenstaden, France|Univ Strasbourg, Illkirch Graffenstaden, France|Ludwig Maximilians Univ Munchen, Gene Ctr, Munich, Germany;

    Univ Strasbourg, CNRS, INSERM,IGBMC, Ctr Integrat Biol CBI,Dept Integrated Struct Biol, 1 Rue Laurent Fries, F-67404 Illkirch Graffenstaden, France|Inst Genet & Mol & Cellular Biol IGBMC, 1 Rue Laurent Fries, Illkirch Graffenstaden, France|CNRS, UMR 7104, Illkirch Graffenstaden, France|INSERM, U964, Illkirch Graffenstaden, France|Univ Strasbourg, Illkirch Graffenstaden, France;

    Univ Strasbourg, CNRS, INSERM,IGBMC, Ctr Integrat Biol CBI,Dept Integrated Struct Biol, 1 Rue Laurent Fries, F-67404 Illkirch Graffenstaden, France|Inst Genet & Mol & Cellular Biol IGBMC, 1 Rue Laurent Fries, Illkirch Graffenstaden, France|CNRS, UMR 7104, Illkirch Graffenstaden, France|INSERM, U964, Illkirch Graffenstaden, France|Univ Strasbourg, Illkirch Graffenstaden, France;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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