Characterization of a cDNA clone encoding the visna virus transactivating protein

J. L. Davis, J. E. Clements

Research output: Contribution to journalArticlepeer-review

50 Scopus citations

Abstract

The unique pathogenesis of lentiviral infections in humans and ruminant animals may be explained, in part, by the complex mechanisms regulating transcription and translation of their viral genes. This report demonstrates that a visna virus-encoded protein transactivates viral gene expression. A 1.4-kilobase cDNA clone encodes two distinct proteins with apparent molecular masses of 21.5 and 10 kDa. We demonstrate that the 10-kDa species is the visna virus transactivating (Tat) protein; the other species may be analogous to the rev (formerly art or trs) gene product of human immunodeficiency virus.

Original languageEnglish (US)
Pages (from-to)414-418
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume86
Issue number2
DOIs
StatePublished - 1989

ASJC Scopus subject areas

  • General

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