| Literature DB >> 33326748 |
Benjamin Lau1, Jingdong Cheng2, Dirk Flemming1, Giuseppe La Venuta1, Otto Berninghausen2, Roland Beckmann3, Ed Hurt4.
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.Entities:
Keywords: 5’ ETS; 90S pre-ribosome; MTR4; exosome; ribosome biogenesis
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Year: 2020 PMID: 33326748 DOI: 10.1016/j.molcel.2020.11.009
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970