Cytosine deamination in SARS-CoV-2 leads to progressive CpG depletion.
KAUST DepartmentBiological and Environmental Sciences and Engineering (BESE) Division
Environmental Science and Engineering Program
King Abdullah University of Science and Technology (KAUST), Pathogen Genomics Laboratory, Biological and Environmental Science and Engineering (BESE), Thuwal8 Jeddah, 23955-6900, Saudi Arabia.
Pathogen Genomics Laboratory
KAUST Grant NumberBAS/1/1020-01-01
Permanent link to this recordhttp://hdl.handle.net/10754/663776
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AbstractRNA viruses use CpG reduction to evade the host cell defense, but the driving mechanism is still largely unknown. To address this, we used rapidly growing genomic dataset of SARS-CoV-2 with relevant metadata information. SARS-CoV-2 genomes show a progressive increase of C-to-U substitutions resulting in CpG loss over just a few months. This is consistent with APOBEC-mediated RNA editing resulting in CpG reduction, thus allowing the virus to escape ZAP-mediated RNA degradation. Our results thus link the dynamics of target sequences in viral genome for two known host molecular defense mechanisms, the APOBEC and ZAP proteins.
CitationSadykov, M., Mourier, T., Guan, Q., & Pain, A. (2020). Cytosine deamination in SARS-CoV-2 leads to progressive CpG depletion. doi:10.1101/2020.06.19.161687
SponsorsWe thank all laboratories which have contributed sequences to the GISAID database and Zhadyra Yerkesh for giving her comments and helpful discussions. This work was supported by funding from King Abdullah University of Science and Technology (KAUST), Office of Sponsored Research (OSR). Work in AP’s laboratory is supported by the KAUST faculty baseline fund (BAS/1/1020-01-01).
PublisherCold Spring Harbor Laboratory