A cofactor, TIP30, specifically enhances HIV-1 Tatactivated transcription
Author(s) -
Hua Xiao,
Yong Tao,
Jack Greenblatt,
Robert G. Roeder
Publication year - 1998
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.95.5.2146
Subject(s) - rna polymerase ii , transactivation , transcription (linguistics) , transcription preinitiation complex , polymerase , microbiology and biotechnology , general transcription factor , coactivator , transcription factor ii d , rna polymerase , biology , chemistry , rna , rna polymerase ii holoenzyme , transcription factor , promoter , gene expression , biochemistry , gene , linguistics , philosophy
Replication of HIV-1 requires the viral Tat protein, which increases the extent of transcription elongation by RNA polymerase II after activation at the single viral long terminal repeat (LTR) promoter. This effect of Tat on transcription requires Tat interactions with a 5' region (TAR) in nascent transcripts as well as Tat-specific cofactors. The present study identifies a cellular protein, TIP30, that interacts with Tat and with an SRB-containing RNA polymerase II complex both in vivo and in vitro. Coexpression of TIP30 specifically enhances transactivation by Tat in transfected cells, and immunodepletion of TIP30 from nuclear extracts abolishes Tat-activated transcription without affecting Tat-independent transcription. These results implicate TIP30 as a specific coactivator that may enhance formation of a Tat-RNA polymerase II holoenzyme complex.
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