SAGA function in tissue-specific gene expression

被引:51
|
作者
Weake, Vikki M. [1 ]
Workman, Jerry L. [1 ]
机构
[1] Stowers Inst Med Res, Kansas City, MO 64110 USA
关键词
IN-VIVO TARGET; RNA-POLYMERASE; H2B UBIQUITYLATION; HISTONE H2B; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTIONAL ACTIVATION; DROSOPHILA-MELANOGASTER; HAT COMPLEXES; PROTEIN; DEUBIQUITINATION;
D O I
10.1016/j.tcb.2011.11.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Spt-Ada-Gcn5-acetyltransferase (SAGA) transcription coactivator plays multiple roles in regulating transcription because of the presence of functionally independent modules of subunits within the complex. We have recently identified a role for the ubiquitin protease activity of SAGA in regulating tissue-specific gene expression in Drosophila. Here, we discuss the modular nature of SAGA and the different mechanisms through which SAGA is recruited to target promoters. We propose that the genes sensitive to loss of the ubiquitin protease activity of SAGA share functional characteristics that require deubiquitination of monoubiquitinated histone H2B (ubH2B) for full activation. We hypothesize that deubiquitination of ubH2B by SAGA destabilizes promoter nucleosomes, thus enhancing recruitment of RNA polymerase II (Pol II) to weak promoters. In addition, SAGA-mediated deubiquitination of ubH2B may facilitate binding of factors that are important for the transition of paused Pol II into transcription elongation.
引用
收藏
页码:177 / 184
页数:8
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