Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 7RH, U.K.
Biochem J. 2018 Dec 14;475(24):3921-3932. doi: 10.1042/BCJ20170314.
At face value, the Sin3 histone deacetylase (HDAC) complex appears to be a prototypical co-repressor complex, that is, a multi-protein complex recruited to chromatin by DNA bound repressor proteins to facilitate local histone deacetylation and transcriptional repression. While this is almost certainly part of its role, Sin3 stubbornly refuses to be pigeon-holed in quite this way. Genome-wide mapping studies have found that Sin3 localises predominantly to the promoters of actively transcribed genes. While Sin3 knockout studies in various species result in a combination of both up- and down-regulated genes. Furthermore, genes such as the stem cell factor, , are dependent on the direct association of Sin3 for active transcription to occur. Sin3 appears to have properties of a co-repressor, co-activator and general transcription factor, and has thus been termed a co-regulator complex. Through a series of unique domains, Sin3 is able to assemble HDAC1/2, chromatin adaptors and transcription factors in a series of functionally and compositionally distinct complexes to modify chromatin at both gene-specific and global levels. Unsurprisingly, therefore, Sin3/HDAC1 have been implicated in the regulation of numerous cellular processes, including mammalian development, maintenance of pluripotency, cell cycle regulation and diseases such as cancer.
从表面上看,Sin3 组蛋白去乙酰化酶 (HDAC) 复合物似乎是一种典型的共抑制复合物,即通过与 DNA 结合的抑制蛋白结合到染色质上,从而募集到多蛋白复合物,以促进局部组蛋白去乙酰化和转录抑制。虽然这几乎肯定是其作用的一部分,但 Sin3 却固执地拒绝被这样归类。全基因组作图研究发现,Sin3 主要定位于转录活跃的基因的启动子上。虽然在各种物种中进行的 Sin3 敲除研究导致了基因的上调和下调的组合。此外,诸如干细胞因子()等基因依赖于 Sin3 的直接结合以进行活性转录。Sin3 似乎具有共抑制因子、共激活因子和一般转录因子的特性,因此被称为共调节复合物。通过一系列独特的结构域,Sin3 能够组装 HDAC1/2、染色质衔接子和转录因子,形成一系列在功能和组成上不同的复合物,以在基因特异性和全局水平上修饰染色质。因此,毫不奇怪,Sin3/HDAC1 被牵连到许多细胞过程的调控中,包括哺乳动物发育、多能性维持、细胞周期调控以及癌症等疾病。