Activation of the JC virus Tat-responsive transcriptional control element by association of the Tat protein of human immunodeficiency virus 1 with cellular protein Purα
Author(s) -
Chavdar Krachmarov,
Lara G. Chepenik,
Sharon Barr-Vagell,
Kamel Khalili,
Edward M. Johnson
Publication year - 1996
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.93.24.14112
Subject(s) - biology , microbiology and biotechnology , transcription (linguistics) , promoter , heterologous , dna , dna replication , virus , viral replication , response element , transcription factor , dna binding protein , hiv long terminal repeat , virology , long terminal repeat , gene , gene expression , genetics , philosophy , linguistics
JC virus is activated to replicate in glial cells of many AIDS patients with neurological disorders. In human glial cells, the human immunodeficiency virus 1 (HIV-1) Tat protein activates the major late promoter of JC virus through a Tat-responsive DNA element, termedupTAR , which is a recognition site for cellular Purα, a sequence-specific single-stranded DNA binding protein implicated in cell cycle control of DNA replication and transcription. Tat interacts with two leucine-rich repeats in Purα to form a complex that can be immunoprecipitated from cell extracts. Tat enhances the ability of purified glutathioneS -transferase-Purα (GST-Purα) to bind theupTAR element. Tat acts synergistically with Purα, in a cell-cycle-dependent manner, to activate transcription at anupTAR element placed upstream of a heterologous promoter. Since Purα is ubiquitously expressed in human cells and sincePUR elements are located near many promoters and origins of replication, the Tat-Purα interaction may be implicated in effects of HIV-1 throughout the full range of HIV-1-infected cells.
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