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The Human Immunodeficiency Virus Transactivator Tat Interacts with the RNA Polymerase II Holoenzyme
Author(s) -
Thomas P. Cujec,
Helen Cho,
Edio Maldonado,
Jon Meyer,
Danny Reinberg,
B. Matija Peterlin
Publication year - 1997
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.17.4.1817
Subject(s) - transactivation , biology , transcription (linguistics) , microbiology and biotechnology , rna polymerase ii , transcription factor ii d , rna polymerase iii , polymerase , rna , hiv long terminal repeat , rna polymerase ii holoenzyme , virology , long terminal repeat , rna dependent rna polymerase , transcription factor , gene expression , gene , promoter , biochemistry , linguistics , philosophy
The human immunodeficiency virus (HIV) encodes a transcriptional transactivator (Tat), which binds to an RNA hairpin called the transactivation response element (TAR) that is located downstream of the site of initiation of viral transcription. Tat stimulates the production of full-length viral transcripts by RNA polymerase II (pol II). In this study, we demonstrate that Tat coimmunoprecipitates with the pol II holoenzyme in cells and that it binds to the purified holoenzyme in vitro. Furthermore, Tat affinity chromatography purifies a holoenzyme from HeLa nuclear extracts which, upon addition of TBP and TFIIB, supports Tat transactivation in vitro, indicating that it contains all the cellular proteins required for the function of Tat. By demonstrating that Tat interacts with the holoenzyme in the absence of TAR, our data suggest a single-step assembly of Tat and the transcription complex on the long terminal repeat of HIV.

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