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Rampant C→U Hypermutation in the Genomes of SARS-CoV-2 and Other Coronaviruses: Causes and Consequences for Their Short- and Long-Term Evolutionary Trajectories

Simmonds, P.·2020·mSphere

Published version of a preprint

Abstract

The wealth of accurately curated sequence data for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), its long genome, and its low substitution rate provides a relatively blank canvas with which to investigate effects of mutational and editing processes imposed by the host cell. The finding that a large proportion of sequence change in SARS-CoV-2 in the initial months of the pandemic comprised C→U mutations in a host APOBEC-like context provides evidence for a potent host-driven antiviral editing mechanism against coronaviruses more often associated with antiretroviral defense. In evolutionary terms, the contribution of biased, convergent, and context-dependent mutations to sequence change in SARS-CoV-2 is substantial, and these processes are not incorporated by standard models used in molecular epidemiology investigations.

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Metadata

Authors
Simmonds, P.
Affiliations
Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom
Venue
mSphere
Published
2020-06-24
Volume
5
Issue
3
ISSN
2379-5042
Cited by
245
References
5
Language
en
Funders
Wellcome Trust (WT103767MA)

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