Hildmann Christian, Riester Daniel, Schwienhorst Andreas
Department of Molecular Genetics and Preparative Molecular Biology, Institute for Microbiology and Genetics, Grisebachstr. 8, 37077, Göttingen, Germany.
Appl Microbiol Biotechnol. 2007 Jun;75(3):487-97. doi: 10.1007/s00253-007-0911-2. Epub 2007 Mar 22.
The elucidation of mechanisms of chromatin remodeling, particular transcriptional activation, and repression by histone acetylation and deacetylation has shed light on the role of histone deacetylases (HDAC) as a new kind of therapeutic target for human cancer treatment. HDACs, in general, act as components of large corepressor complexes that prevent the transcription of several tumor suppression genes. In addition, they appear to be also involved in the deacetylation of nonhistone proteins. This paper reviews the most recent insights into the diverse biological roles of HDACs as well as the evolution of this important protein family.
对染色质重塑机制,特别是组蛋白乙酰化和去乙酰化介导的转录激活与抑制机制的阐明,为组蛋白去乙酰化酶(HDAC)作为人类癌症治疗的新型治疗靶点的作用提供了线索。一般来说,HDAC作为大型共抑制复合物的组成部分,可阻止多种肿瘤抑制基因的转录。此外,它们似乎还参与非组蛋白的去乙酰化过程。本文综述了对HDAC多样生物学作用的最新见解以及这个重要蛋白质家族的进化情况。