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PMID: 1315144 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

A comparison of regulatory features in primate lentiviruses.

AIDS research and human retroviruses ·Vol. 8 ·No. 3 ·1992-03-00 ·Pages 387-93

Cullen BR, Garrett ED

Abstract

Historically, research into the regulation of gene expression in primate lentiviruses has focused on human immunodeficiency virus type 1 (HIV-1), the primary cause of acquired immunodeficiency syndrome (AIDS) in humans. The increasing emergence of HIV-2 as a human pathogen, and the importance of the various simian immunodeficiency viruses (SIV) as models for the treatment and prevention of HIV-1-induced disease, suggest that an understanding of gene regulation in these related viruses will become increasingly important. Here, the present state of knowledge in this latter field is reviewed. In general, while the data support the hypothesis that viral gene expression is regulated by very similar mechanisms in all primate lentiviruses, it also is clear that differences in detail do exist. These differences may influence the pathogenic potential of the different strains of primate lentiviruses and must be considered in evaluating SIV as an appropriate in vivo model for HIV-1.

MeSH Terms
Amino Acid Sequence Base Sequence Gene Expression Regulation, Viral/genetics,physiology Gene Products, rev/metabolism Gene Products, tat/metabolism HIV Enhancer/physiology Lentivirus/genetics Molecular Sequence Data NF-kappa B/metabolism RNA, Viral/genetics,metabolism
Chemicals
Gene Products, rev Gene Products, tat NF-kappa B RNA, Viral
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cullen B R
Howard Hughes Medical Institute, Section of Genetics, Duke University Medical Center, Durham, NC 27710.
Garrett E D
Article Info
Journal
AIDS research and human retroviruses
Abbr.
AIDS Res Hum Retroviruses
ISSN
0889-2229
Published
1992-03-00
Pages
387-93
Language
English
Region
United States
NLM ID
8709376
Subset
IM
Grants
NIAID NIH HHS · AI28233 · United States
NIAID NIH HHS · AI28662 · United States
NIAID NIH HHS · AI29821 · United States
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