A cofactor, TIP30, specifically enhances HIV-1 Tat-activated transcription

被引:69
作者
Xiao, H
Tao, Y
Greenblatt, J
Roeder, RG [1 ]
机构
[1] Rockefeller Univ, Biochem & Mol Biol Lab, New York, NY 10021 USA
[2] Univ Toronto, Banting & Best Dept Med Res, Toronto, ON M5G 1L6, Canada
[3] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5G 1L6, Canada
关键词
D O I
10.1073/pnas.95.5.2146
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:2146 / 2151
页数:6
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