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组蛋白去乙酰化酶复合物:结构、调控与功能。

Histone deacetylase complexes: Structure, regulation and function.

机构信息

Department of Pharmacology, School of Basic Medical Sciences, State Key Laboratory for Esophageal Cancer Prevention and Treatment, Zhengzhou University, Zhengzhou, Henan Province 450001, China.

Key Laboratory of Advanced Drug Preparation Technologies, Ministry of Education of China, Collaborative Innovation Center of New Drug Research and Safety Evaluation, Henan Province, Key Laboratory of Henan Province for Drug Quality and Evaluation, Institute of Drug Discovery and Development, School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan Province 450001, China.

出版信息

Biochim Biophys Acta Rev Cancer. 2024 Sep;1879(5):189150. doi: 10.1016/j.bbcan.2024.189150. Epub 2024 Jul 4.


DOI:10.1016/j.bbcan.2024.189150
PMID:38971208
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.

摘要

组蛋白去乙酰化酶(HDACs)是关键的表观遗传调控因子,具有去乙酰化酶功能的转录复合物是核内表观遗传核心抑制复合物之一,靶向表观基因组。含有 HDAC 的核心抑制复合物,如 Sin3 复合物、NuRD 复合物、CoREST 复合物和 SMRT/NCoR 复合物,在生物系统中很常见。这些复合物以单一状态激活原本无活性的 HDAC。HDAC 复合物在转录、复制和 DNA 修复等关键生物过程的调节中发挥着重要作用。此外,HDAC 复合物功能失调与包括癌症在内的人类疾病有关。目前正在积极寻求针对 HDAC 复合物的治疗策略。因此,阐明 HDAC 复合物的性质和组成对于理解其在生理和病理条件下功能的分子基础,以及设计靶向治疗至关重要。本综述介绍了大型多蛋白 HDAC 结合复合物的关键方面,包括其结构、功能、调节机制、在疾病发展中的作用以及在治疗中的作用。

相似文献

[1]
Histone deacetylase complexes: Structure, regulation and function.

Biochim Biophys Acta Rev Cancer. 2024-9

[2]
Physiological roles of class I HDAC complex and histone demethylase.

J Biomed Biotechnol. 2011

[3]
Eloquent silence: developmental functions of Class I histone deacetylases.

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[4]
Role of HDACs in normal and malignant hematopoiesis.

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[5]
CoREST is an integral component of the CoREST- human histone deacetylase complex.

Proc Natl Acad Sci U S A. 2001-2-13

[6]
Distinct biochemical properties of the class I histone deacetylase complexes.

Curr Opin Chem Biol. 2022-10

[7]
NuRD and SIN3 histone deacetylase complexes in development.

Trends Genet. 2000-8

[8]
Diverse nucleosome Site-Selectivity among histone deacetylase complexes.

Elife. 2020-6-5

[9]
A feed-forward repression mechanism anchors the Sin3/histone deacetylase and N-CoR/SMRT corepressors on chromatin.

Mol Cell Biol. 2006-7

[10]
In vitro targeting reveals intrinsic histone tail specificity of the Sin3/histone deacetylase and N-CoR/SMRT corepressor complexes.

Mol Cell Biol. 2004-3

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[2]
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J Cancer. 2025-7-24

[3]
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J Microbiol Biotechnol. 2025-8-18

[4]
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[5]
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[6]
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[7]
Loss of TACC2 impairs chemokine CCL3 and CCL4 expression and reduces response to anti-PD-1 therapy in soft tissue sarcoma.

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Butyrate Prevents Obesity Accompanied by HDAC9-Mediated Browning of White Adipose Tissue.

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[10]
Acetylation-enhanced Sp1 transcriptional activity suppresses Mlph expression.

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