AI Article Synopsis

  • Ribosome assembly involves various factors and irreversible pre-rRNA processing, leading to the formation of mature ribosomal subunits, with the removal of the 5' external transcribed spacer (5'-ETS) being a key early step.
  • The 5'-ETS is cleaved from the 18S rRNA in the 90S pre-ribosome structure, and this process involves the RNA exosome, a significant exoribonuclease complex.
  • Biochemical analyses and cryo-electron microscopy reveal that the RNA exosome interacts with the 90S pre-ribosome through its co-factor Mtr4 helicase, highlighting the exosome's role in remodeling the pre-ribosome for efficient ribosome synthesis

Article 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, A, 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.

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Source
http://dx.doi.org/10.1016/j.molcel.2020.11.009DOI Listing

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