Literature DB >> 34172362

The enzymes for genome size increase and maintenance of large (+)RNA viruses.

François Ferron1, Bhawna Sama2, Etienne Decroly2, Bruno Canard3.   

Abstract

With sizes <50 kb, viral RNA genomes are at the crossroads of genetic, biophysical, and biochemical stability in their host cell. Here, we analyze the enzymatic assets accompanying large RNA genome viruses, mostly based on recent scientific advances in Coronaviridae. We argue that, in addition to the presence of an RNA exonuclease (ExoN), two markers for the large size of viral RNA genomes are (i) the presence of one or more RNA methyltransferases (MTases) and (ii) a specific architecture of the RNA-dependent RNA polymerase active site. We propose that RNA genome expansion and maintenance are driven by an evolutionary ménage-à-trois made of fast and processive RNA polymerases, RNA repair ExoNs, and RNA MTases that relates to the transition between RNA- to DNA-based life.
Copyright © 2021. Published by Elsevier Ltd.

Entities:  

Keywords:  RNA exonuclease; RNA methyltransferase; RNA world; RNA-dependent RNA polymerase; fidelity; innate immunity

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Year:  2021        PMID: 34172362     DOI: 10.1016/j.tibs.2021.05.006

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  1 in total

1.  The SARS-CoV nsp12 Polymerase Active Site Is Tuned for Large-Genome Replication.

Authors:  Grace Campagnola; Vishnu Govindarajan; Annelise Pelletier; Bruno Canard; Olve B Peersen
Journal:  J Virol       Date:  2022-08-04       Impact factor: 6.549

  1 in total

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