Parra Maribel
Cellular Differentiation Group, Cancer Epigenetics and Biology Program, Bellvitge Biomedical Research Institute, Barcelona, Spain.
FEBS J. 2015 May;282(9):1736-44. doi: 10.1111/febs.13061. Epub 2014 Oct 27.
HDAC4, 5, 7 and 9 constitute the class IIa histone deacetylases (HDACs) within the large family of protein deacetylases. Class IIa HDACs have unique features that distinguish them from other HDACs. They contain an N-terminal domain that is required for their interaction with tissue-specific transcription factors and recruitment to their target genes. The N-terminal domain on class IIa HDACs also bears conserved serine residues that undergo signal-dependent phosphorylation, which brings about nuclear export of the enzymes and de-repression of their targets. One of the most important aspects of class IIa HDACs is their expression in specific tissues and organs within the organism, where they have crucial roles in development and differentiation processes. This review brings up to date our knowledge of the physiological and pathological functions of class IIa HDACs, focusing in particular on the most recent discoveries from in vivo studies of mouse model systems.
HDAC4、HDAC5、HDAC7和HDAC9构成了蛋白质脱乙酰酶大家族中的IIa类组蛋白脱乙酰酶(HDAC)。IIa类HDAC具有使其有别于其他HDAC的独特特征。它们含有一个N端结构域,该结构域是其与组织特异性转录因子相互作用并募集至其靶基因所必需的。IIa类HDAC的N端结构域还带有保守的丝氨酸残基,这些残基会发生信号依赖性磷酸化,从而导致这些酶的核输出及其靶标的去抑制。IIa类HDAC最重要的一个方面是它们在生物体特定组织和器官中的表达,它们在发育和分化过程中发挥着关键作用。本综述更新了我们对IIa类HDAC生理和病理功能的认识,尤其关注小鼠模型系统体内研究的最新发现。