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PMID: 7543593 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Modification of retroviral RNA by double-stranded RNA adenosine deaminase.

Journal of virology ·Vol. 69 ·No. 9 ·1995-09-00 ·Pages 5878-82

Hajjar AM, Linial ML

Abstract

In this report, we describe a recombinant provirus generated during in vitro passage that contains a short region of adenosine-to-guanosine hypermutation. The hypermutated region is restricted to complementary sequences present in the recombinant provirus. We propose that a duplex was formed in the recombinant RNA prior to reverse transcription. This duplex was a substrate for double-stranded RNA adenosine deaminase, an activity found in all cells examined that deaminates A in double-stranded RNA, converting it to inosine, which is further converted to a guanosine by reverse transcription. It appears that cis viral sequences facilitated the A-->G transitions.

Related Genes
MeSH Terms
Adenosine Adenosine Deaminase/metabolism Animals Avian Sarcoma Viruses/genetics Base Sequence Cell Line DNA Primers Genes, env Genes, pol Guanosine Molecular Sequence Data Mutation Polymerase Chain Reaction Proviruses/genetics Quail RNA/biosynthesis,metabolism RNA, Antisense RNA, Viral/biosynthesis,metabolism RNA-Binding Proteins Repetitive Sequences, Nucleic Acid Substrate Specificity
Chemicals
DNA Primers RNA, Antisense RNA, Viral RNA, recombinant RNA-Binding Proteins Guanosine RNA ADARB1 protein, human Adenosine Deaminase Adenosine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hajjar A M
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Linial M L
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1995-09-00
Pages
5878-82
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC189466
Subset
IM
Grants
NCI NIH HHS · CA18282 · United States
NCI NIH HHS · P30CA15704 · United States
NCRR NIH HHS · RR00079 · United States
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