Department of Biochemistry and Molecular Biology and the Howard Hughes Medical Institute, Colorado State University, Fort Collins, Colorado 80523-1870, USA.
J Biol Chem. 2011 May 27;286(21):18369-74. doi: 10.1074/jbc.R110.180778. Epub 2011 Mar 24.
Changes in chromatin architecture induced by epigenetic mechanisms are essential for normal cellular processes such as gene expression, DNA repair, and cellular division. Compact chromatin presents a barrier to these processes and is highly regulated by epigenetic markers binding to components of the nucleosome. Histone modifications directly influence chromatin dynamics and facilitate recruitment of additional factors such as chromatin remodelers and histone chaperones. One member of this last class of factors, FACT (facilitates chromatin transcription), is categorized as a histone chaperone critical for nucleosome reorganization during replication, transcription, and DNA repair. Significant discoveries regarding the role of histone chaperones and specifically FACT have come over the past dozen years from a number of independent laboratories. Here, we review the structural and biophysical basis for FACT-mediated nucleosome reorganization and discuss up-to-date models for FACT function.
表观遗传机制诱导的染色质结构变化对于正常的细胞过程(如基因表达、DNA 修复和细胞分裂)是必不可少的。紧凑的染色质对这些过程构成了障碍,并且受到与核小体成分结合的表观遗传标记的高度调控。组蛋白修饰直接影响染色质动力学,并促进其他因子(如染色质重塑因子和组蛋白伴侣)的募集。在最后一类因子中,FACT(促进染色质转录)被归类为组蛋白伴侣,在复制、转录和 DNA 修复过程中对于核小体重排至关重要。过去十几年,来自多个独立实验室的研究取得了关于组蛋白伴侣,特别是 FACT 作用的重要发现。在这里,我们回顾了 FACT 介导的核小体重排的结构和生物物理基础,并讨论了 FACT 功能的最新模型。