Document 0457 DOCN M9650457 TI NF-kappa B-mediated chromatin reconfiguration and transcriptional activation of the HIV-1 enhancer in vitro. DT 9605 AU Pazin MJ; Sheridan PL; Cannon K; Cao Z; Keck JG; Kadonaga JT; Jones KA; Department of Biology, University of California, San Diego; (UCSD), La Jolla 92093-0347, USA. SO Genes Dev. 1996 Jan 1;10(1):37-49. Unique Identifier : AIDSLINE MED/96136707 AB NF-kappa B is a potent inducible transcription factor that regulates many genes in activated T cells. In this report we examined the ability of different subunits of NF-kappa B to enhance HIV-1 transcription in vitro with chromatin templates. We find that the p65 subunit of NF-kappa B is a strong transcriptional activator of nucleosome-assembled HIV-1 DNA, whereas p50 does not activate transcription, and that p65 activates transcription synergistically with Sp1 and distal HIV-1 enhancer-binding factors (LEF-1, Ets-1, and TFE-3). These effects were observed with chromatin, but not with nonchromatin templates. Furthermore, binding of either p50 or p65 with Sp1 induces rearrangement of the chromatin to a structure that resembles the one reported previously for integrated HIV-1 proviral DNA in vivo. These results suggest that p50 and Sp1 contribute to the establishment of the nucleosomal arrangement of the uninduced provirus in resting T cells, and that p65 activates transcription by recruitment of the RNA polymerase II transcriptional machinery to the chromatin-repressed basal promoter. DE Base Sequence Binding Sites Chromatin/CHEMISTRY/*GENETICS/METABOLISM Comparative Study DNA-Binding Proteins/GENETICS *Gene Expression Regulation, Viral Hela Cells Human HIV Enhancer/*GENETICS HIV Long Terminal Repeat Molecular Sequence Data Nucleosomes/GENETICS NF-kappa B/CHEMISTRY/*GENETICS/ISOLATION & PURIF/METABOLISM Repetitive Sequences, Nucleic Acid Support, Non-U.S. Gov't Support, U.S. Gov't, Non-P.H.S. Support, U.S. Gov't, P.H.S. Trans-Activators Transcription Factor, Sp1/GENETICS/METABOLISM Transcription Factors/GENETICS/METABOLISM *Transcription, Genetic JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).