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PMID: 2596032 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Analysis of the function of viral protein X (VPX) of HIV-2.

Virology ·Vol. 173 ·No. 2 ·1989-12-00 ·Pages 624-30

Hu W, Vander Heyden N, Ratner L

Abstract

To investigate the function of vpx, a gene in HIV-2 and SIV, but not in HIV-1, three site-directed mutants (pMX) were constructed from a functional proviral HIV-2 plasmid clone (pSE). Transfection of COS-1 cells with all three mutants as well as pSE gave rise to equivalent amounts of virus. Each virus could be passaged in H9 and CEM lymphoid cell lines, peripheral blood lymphocytes, and monocytes with equal efficiency and demonstrated similar cytopathic effects. Hybridization data with DAN from the infected cells demonstrated the presence of similar levels of viral sequences and the mutations in each of the MX-infected cell lines. Immunoprecipitation analysis demonstrated a 16-kDa VPX protein in cells infected with SE virus, as well as in the virus particles, but not in cells infected with MX viruses or the particles themselves. However, equivalent levels of gag and env proteins were demonstrated in all infected cells and virion preparations. These data suggest that VPX is dispensable for virus replication and cytopathicity.

MeSH Terms
Amino Acid Sequence Base Sequence Blotting, Southern Cell Line Cytopathogenic Effect, Viral DNA, Viral/genetics Gene Expression Regulation, Viral HIV-2/genetics,physiology Humans Molecular Sequence Data Mutation Nucleic Acid Hybridization Plasmids RNA, Viral/biosynthesis Radioimmunoprecipitation Assay Restriction Mapping Transfection Virion/genetics Virus Replication
Chemicals
DNA, Viral RNA, Viral
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hu W
Department of Medicine, Washington University, St. Louis, Missouri 63110.
Vander Heyden N
Ratner L
Article Info
Journal
Virology
Abbr.
Virology
ISSN
0042-6822
Published
1989-12-00
Pages
624-30
Language
English
Region
United States
NLM ID
0110674
Subset
IM
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