Mahmoudi Tokameh, Parra Maribel, Vries Robert G J, Kauder Steven E, Verrijzer C Peter, Ott Melanie, Verdin Eric
Gladstone Institute of Virology and Immunology, University of California, San Francisco, California 94158, USA.
J Biol Chem. 2006 Jul 21;281(29):19960-8. doi: 10.1074/jbc.M603336200. Epub 2006 May 10.
Tat is a critical viral transactivator essential for human immunodeficiency virus (HIV) gene expression. Activation involves binding to an RNA stem-loop structure and recruitment of the positive transcription elongation factor b. Tat also induces the remodeling of a single nucleosome in the HIV promoter. However, the mechanism of this remodeling has remained unclear. Knockdown of INI-1 and BRG-1, two components of the SWI/SNF chromatin-remodeling complex, suppressed Tat-mediated transactivation. Cells lacking INI-1 (G401 and MON) or BRG-1 (C33A) exhibited defective transactivation by Tat that was restored upon INI-1 and BRG-1 expression, respectively. Tat was co-immunoprecipitated with several SWI/SNF subunits, including INI-1, BRG-1, and beta-actin. The SWI/SNF complex interacted with the integrated HIV promoter in a Tat-dependent manner. We also found that INI-1 and BRG-1 synergized with the p300 acetyltransferase to activate the HIV promoter. This synergism depended on the acetyltransferase activity of p300 and on Tat Lys(50) and Lys(51). In conclusion, Tat-mediated activation of the HIV promoter requires the SWI/SNF complex in synergy with the coactivator p300.
Tat是一种对人类免疫缺陷病毒(HIV)基因表达至关重要的病毒反式激活因子。激活过程涉及与一个RNA茎环结构结合以及募集正转录延伸因子b。Tat还能诱导HIV启动子中单个核小体的重塑。然而,这种重塑的机制仍不清楚。敲低SWI/SNF染色质重塑复合物的两个组分INI-1和BRG-1,可抑制Tat介导的反式激活。缺乏INI-1(G401和MON)或BRG-1(C33A)的细胞表现出Tat介导的反式激活缺陷,分别在INI-1和BRG-1表达后得以恢复。Tat与包括INI-1、BRG-1和β-肌动蛋白在内的多个SWI/SNF亚基共免疫沉淀。SWI/SNF复合物以Tat依赖的方式与整合的HIV启动子相互作用。我们还发现INI-1和BRG-1与p300乙酰转移酶协同激活HIV启动子。这种协同作用依赖于p300的乙酰转移酶活性以及Tat的赖氨酸50和赖氨酸51。总之,Tat介导的HIV启动子激活需要SWI/SNF复合物与辅激活因子p300协同作用。