Verdin Eric, Dequiedt Franck, Kasler Herbert G
Gladstone Institute of Virology and Immunology, University of California San Francisco, PO Box 419100, San Francisco, CA 94141, USA.
Trends Genet. 2003 May;19(5):286-93. doi: 10.1016/S0168-9525(03)00073-8.
Histone acetylation and deacetylation play essential roles in modifying chromatin structure and regulating gene expression in eukaryotes. Histone deacetylases (HDACs) catalyze the deacetylation of lysine residues in the histone N-terminal tails and are found in large multiprotein complexes with transcriptional co-repressors. Human HDACs are grouped into three classes based on their similarity to known yeast factors: class I HDACs are similar to the yeast transcriptional repressor yRPD3, class II HDACs to yHDA1 and class III HDACs to ySIR2. In this review, we focus on the biology of class II HDACs. These newly discovered enzymes have been implicated as global regulators of gene expression during cell differentiation and development. We discuss their emerging biological functions and the molecular mechanisms by which they are regulated.
组蛋白乙酰化和去乙酰化在真核生物中修饰染色质结构和调节基因表达方面发挥着重要作用。组蛋白去乙酰化酶(HDACs)催化组蛋白N端尾巴中赖氨酸残基的去乙酰化反应,并且存在于与转录共抑制因子形成的大型多蛋白复合物中。人类HDACs根据其与已知酵母因子的相似性分为三类:I类HDACs与酵母转录抑制因子yRPD3相似,II类HDACs与yHDA1相似,III类HDACs与ySIR2相似。在本综述中,我们重点关注II类HDACs的生物学特性。这些新发现的酶被认为是细胞分化和发育过程中基因表达的全局调节因子。我们讨论了它们新出现的生物学功能以及其调控的分子机制。