Your browser doesn't support javascript.
loading
Structure of the Maturing 90S Pre-ribosome in Association with the RNA Exosome.
Lau, Benjamin; Cheng, Jingdong; Flemming, Dirk; La Venuta, Giuseppe; Berninghausen, Otto; Beckmann, Roland; Hurt, Ed.
Afiliação
  • Lau B; Heidelberg University Biochemistry Center (BZH), Im Neuenheimer Feld 328, 69120 Heidelberg, Germany.
  • Cheng J; Gene Center, Department of Biochemistry and Center for Integrated Protein Science Munich (CiPSM), Ludwig-Maximilians-Universität München, Feodor-Lynen-Straße 25, 81377 Munich, Germany.
  • Flemming D; Heidelberg University Biochemistry Center (BZH), Im Neuenheimer Feld 328, 69120 Heidelberg, Germany.
  • La Venuta G; Heidelberg University Biochemistry Center (BZH), Im Neuenheimer Feld 328, 69120 Heidelberg, Germany.
  • Berninghausen O; Gene Center, Department of Biochemistry and Center for Integrated Protein Science Munich (CiPSM), Ludwig-Maximilians-Universität München, Feodor-Lynen-Straße 25, 81377 Munich, Germany.
  • Beckmann R; Gene Center, Department of Biochemistry and Center for Integrated Protein Science Munich (CiPSM), Ludwig-Maximilians-Universität München, Feodor-Lynen-Straße 25, 81377 Munich, Germany. Electronic address: beckmann@genzentrum.lmu.de.
  • Hurt E; Heidelberg University Biochemistry Center (BZH), Im Neuenheimer Feld 328, 69120 Heidelberg, Germany. Electronic address: ed.hurt@bzh.uni-heidelberg.de.
Mol Cell ; 81(2): 293-303.e4, 2021 01 21.
Article em En | MEDLINE | ID: mdl-33326748
ABSTRACT
Ribosome assembly is catalyzed by numerous trans-acting factors and coupled with irreversible pre-rRNA processing, driving the pathway toward mature ribosomal subunits. One decisive step early in this progression is removal of the 5' external transcribed spacer (5'-ETS), an RNA extension at the 18S rRNA that is integrated into the huge 90S pre-ribosome structure. Upon endo-nucleolytic cleavage at an internal site, A1, the 5'-ETS is separated from the 18S rRNA and degraded. Here we present biochemical and cryo-electron microscopy analyses that depict the RNA exosome, a major 3'-5' exoribonuclease complex, in a super-complex with the 90S pre-ribosome. The exosome is docked to the 90S through its co-factor Mtr4 helicase, a processive RNA duplex-dismantling helicase, which strategically positions the exosome at the base of 5'-ETS helices H9-H9', which are dislodged in our 90S-exosome structures. These findings suggest a direct role of the exosome in structural remodeling of the 90S pre-ribosome to drive eukaryotic ribosome synthesis.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ribossomos / Saccharomyces cerevisiae / RNA Ribossômico 18S / Proteínas de Saccharomyces cerevisiae / Endorribonucleases / Exonucleases / RNA Helicases DEAD-box / Complexo Multienzimático de Ribonucleases do Exossomo Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Cell Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ribossomos / Saccharomyces cerevisiae / RNA Ribossômico 18S / Proteínas de Saccharomyces cerevisiae / Endorribonucleases / Exonucleases / RNA Helicases DEAD-box / Complexo Multienzimático de Ribonucleases do Exossomo Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Cell Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha