Transcription through the HIV-1 nucleosomes: Effects of the PBAF complex in Tat activated transcription

被引:45
|
作者
Easley, Rebecca
Carpio, Lawrence
Dannenberg, Luke
Choi, Soyun
Alani, Dowser
Van Duyne, Rachel
Guendel, Irene
Klase, Zachary [2 ]
Agbottah, Emmanuel
Kehn-Hall, Kylene [1 ]
Kashanchi, Fatah [1 ]
机构
[1] George Mason Univ, Natl Ctr Biodef & Infect Dis, Dept Mol & Microbiol, Manassas, VA 20110 USA
[2] NIAID, NIH, Bethesda, MD 20892 USA
关键词
HW-1; Chromatin; BAF; PBAF; FACT; Transcription; Remodel; IMMUNODEFICIENCY-VIRUS TYPE-1; CHROMATIN-REMODELING COMPLEX; LONG TERMINAL REPEAT; RNA-POLYMERASE-II; ELONGATION-FACTORS; IN-VIVO; SACCHAROMYCES-CEREVISIAE; CHD1; INTERACTS; N-COR; PROTEIN;
D O I
10.1016/j.virol.2010.06.009
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The SWI/SNF complex remodels nucleosomes, allowing RNA Polymerase II access to the HIV-1 proviral DNA. It has not been determined which SWI/SNF complex (BAF or PBAF) remodels nucleosomes at the transcription start site. These complexes differ in only three subunits and determining which subunit(s) is required could explain the regulation of Tat activated transcription. We show that PBAF is required for chromatin remodeling at the nuc-1 start site and transcriptional elongation. We find that Baf200 is required to ensure activation at the LTR level and for viral production. Interestingly, the BAF complex was observed on the LTR whereas PBAF was present on both LTR and Env regions. We found that Tat activated transcription facilitates removal of histones H2A and H2B at the LTR, and that the FACT complex may be responsible for their removal. Finally, the BAF complex may play an important role in regulating splicing of the HIV-1 genome. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:322 / 333
页数:12
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