| Literature DB >> 2072452 |
M H Malim1, D F McCarn, L S Tiley, B R Cullen.
Abstract
Replication of human immunodeficiency virus type 1 requires the functional expression of the virally encoded Rev protein. The binding of this nuclear trans activator to its viral target sequence, the Rev-response element, induces the cytoplasmic expression of unspliced viral mRNAs. Mutation of the activation domain of Rev generates inactive proteins with normal RNA binding capabilities that inhibit wild-type Rev function in a trans-dominant manner. Here, we report that the activation domain comprises a minimum of nine amino acids, four of which are critically spaced leucines. The preservation of this essential sequence in other primate and nonprimate lentivirus Rev proteins indicates that this leucine-rich motif has been highly conserved during evolution. This conclusion, taken together with the observed permissiveness of a variety of eukaryotic cell types for Rev function, suggests that the target for the activation domain of Rev is likely to be a highly conserved cellular protein(s) intrinsic to nuclear mRNA transport or splicing.Entities:
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Year: 1991 PMID: 2072452 PMCID: PMC248862 DOI: 10.1128/JVI.65.8.4248-4254.1991
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103