The low abundance of CpG in the SARS-CoV-2 genome is not an evolutionarily signature of ZAP.
Sci Rep
; 12(1): 2420, 2022 02 14.
Article
in English
| MEDLINE | ID: covidwho-1684102
ABSTRACT
The zinc finger antiviral protein (ZAP) is known to restrict viral replication by binding to the CpG rich regions of viral RNA, and subsequently inducing viral RNA degradation. This enzyme has recently been shown to be capable of restricting SARS-CoV-2. These data have led to the hypothesis that the low abundance of CpG in the SARS-CoV-2 genome is due to an evolutionary pressure exerted by the host ZAP. To investigate this hypothesis, we performed a detailed analysis of many coronavirus sequences and ZAP RNA binding preference data. Our analyses showed neither evidence for an evolutionary pressure acting specifically on CpG dinucleotides, nor a link between the activity of ZAP and the low CpG abundance of the SARS-CoV-2 genome.
Full text:
Available
Collection:
International databases
Database:
MEDLINE
Main subject:
Dinucleoside Phosphates
/
RNA-Binding Proteins
/
Genome, Viral
/
SARS-CoV-2
/
COVID-19
Limits:
Animals
/
Humans
Language:
English
Journal:
Sci Rep
Year:
2022
Document Type:
Article
Affiliation country:
S41598-022-06046-5
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