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Review
. 2024 Sep;1879(5):189150.
doi: 10.1016/j.bbcan.2024.189150. Epub 2024 Jul 4.

Histone deacetylase complexes: Structure, regulation and function

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Review

Histone deacetylase complexes: Structure, regulation and function

Moges Dessale Asmamaw et al. Biochim Biophys Acta Rev Cancer. 2024 Sep.

Abstract

Histone deacetylases (HDACs) are key epigenetic regulators, and transcriptional complexes with deacetylase function are among the epigenetic corepressor complexes in the nucleus that target the epigenome. HDAC-bearing corepressor complexes such as the Sin3 complex, NuRD complex, CoREST complex, and SMRT/NCoR complex are common in biological systems. These complexes activate the otherwise inactive HDACs in a solitary state. HDAC complexes play vital roles in the regulation of key biological processes such as transcription, replication, and DNA repair. Moreover, deregulated HDAC complex function is implicated in human diseases including cancer. Therapeutic strategies targeting HDAC complexes are being sought actively. Thus, illustration of the nature and composition of HDAC complexes is vital to understanding the molecular basis of their functions under physiologic and pathologic conditions, and for designing targeted therapies. This review presents key aspects of large multiprotein HDAC-bearing complexes including their structure, function, regulatory mechanisms, implication in disease development, and role in therapeutics.

Keywords: CoREST complex; Histone deacetylase; NuRD complex; SMRT/NCoR complex; Sin3 complex.

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Conflict of interest statement

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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