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PMID: 2760980 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Temporal aspects of DNA and RNA synthesis during human immunodeficiency virus infection: evidence for differential gene expression.

Journal of virology ·Vol. 63 ·No. 9 ·1989-09-00 ·Pages 3708-13

Kim SY, Byrn R, Groopman J, Baltimore D

Abstract

The kinetics of retroviral DNA and RNA synthesis are parameters vital to understanding viral growth, especially for human immunodeficiency virus (HIV), which encodes several of its own regulatory genes. We have established a single-cycle growth condition for HIV in H9 cells, a human CD4+ lymphocyte line. The full-length viral linear DNA is first detectable by 4 h postinfection. During a one-step growth of HIV, amounts of viral DNA gradually increase until 8 to 12 h postinfection and then decrease. The copy number of unintegrated viral DNA is not extraordinarily high even at its peak. Most strikingly, there is a temporal program of RNA accumulation: the earliest RNA is greatly enriched in the 2-kilobase subgenomic mRNA species, while the level of 9.2-kilobase RNA which is both genomic RNA and mRNA remains low until after 24 h of infection. Virus production begins at about 24 h postinfection. Thus, viral DNA synthesis is as rapid as for other retroviruses, but viral RNA synthesis involves temporal alteration in the species that accumulate, presumably as a consequence of viral regulatory genes.

MeSH Terms
Cell Line DNA, Viral/biosynthesis Gene Expression Regulation HIV/genetics,growth & development Humans RNA, Viral/biosynthesis
Chemicals
DNA, Viral RNA, Viral
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kim S Y
Whitehead Institute for Biomedical Research, Nine Cambridge Center, Massachusetts 02142.
Byrn R
Groopman J
Baltimore D
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1989-09-00
Pages
3708-13
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC250962
Subset
IM
Grants
NHLBI NIH HHS · HL33774 · United States
NHLBI NIH HHS · HL41374 · United States
NHLBI NIH HHS · HL42112 · United States
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