Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1996 Jul;70(7):4871-6.
doi: 10.1128/JVI.70.7.4871-4876.1996.

Inhibition of human immunodeficiency virus type 1 replication is enhanced by a combination of transdominant Tat and Rev proteins

Affiliations

Inhibition of human immunodeficiency virus type 1 replication is enhanced by a combination of transdominant Tat and Rev proteins

C Ulich et al. J Virol. 1996 Jul.

Abstract

Mutation of either of two critical human immunodeficiency virus type 1 (HIV-1) regulatory proteins, Tat and Rev, results in marked defects in viral replication. Thus, inhibition of the function of one or both of these proteins can significantly inhibit viral growth. In the present study, we constructed a novel transdominant Tat mutant protein and compared its efficiency in inhibiting HIV-1 replication with that of transdominant mutant Rev M10 when these proteins were stably expressed either alone or in combination in T-lymphocyte cell lines. The transdominant Tat mutant protein alone resulted in a modest inhibition of HIV replication, but it was able to enhance the ability of the M10 Rev mutant protein to inhibit HIV-1 replication. These results suggest a possible synergistic effect of these transdominant mutant proteins in inhibiting HIV-1 replication.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Science. 1984 May 4;224(4648):497-500 - PubMed
    1. J Virol. 1992 Apr;66(4):1849-55 - PubMed
    1. Nature. 1986 Mar 27-Apr 2;320(6060):367-71 - PubMed
    1. Nature. 1986 May 22-28;321(6068):412-7 - PubMed
    1. Cell. 1986 Sep 12;46(6):807-17 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources