Histone Deacetylase 9: Its Role in the Pathogenesis of Diabetes and Other Chronic Diseases
As a member of the class IIa histone deacetylases (HDACs), HDAC9 catalyzes the deacetylation of histones and transcription factors, commonly leading to the suppression of gene transcription. The activity of HDAC9 is regulated transcriptionally and post-translationally. HDAC9 is known to play an esse...
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Published in | Diabetes & metabolism journal Vol. 44; no. 2; pp. 234 - 244 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
Korean Diabetes Association / Daehan Dangnyobyeong Hakoe
01.04.2020
Korean Diabetes Association 대한당뇨병학회 |
Subjects | |
Online Access | Get full text |
ISSN | 2233-6079 2233-6087 2233-6087 |
DOI | 10.4093/dmj.2019.0243 |
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Abstract | As a member of the class IIa histone deacetylases (HDACs), HDAC9 catalyzes the deacetylation of histones and transcription factors, commonly leading to the suppression of gene transcription. The activity of HDAC9 is regulated transcriptionally and post-translationally. HDAC9 is known to play an essential role in regulating myocyte and adipocyte differentiation and cardiac muscle development. Also, recent studies have suggested that HDAC9 is involved in the pathogenesis of chronic diseases, including cardiovascular diseases, osteoporosis, autoimmune disease, cancer, obesity, insulin resistance, and liver fibrosis. HDAC9 modulates the expression of genes related to the pathogenesis of chronic diseases by altering chromatin structure in their promotor region or reducing the transcriptional activity of their respective transcription factors. This review summarizes the current knowledge of the regulation of HDAC9 expression and activity. Also, the roles of HDAC9 in the pathogenesis of chronic diseases are discussed, along with potential underlying mechanisms. |
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AbstractList | As a member of the class IIa histone deacetylases (HDACs), HDAC9 catalyzes the deacetylation of histones and transcription factors, commonly leading to the suppression of gene transcription. The activity of HDAC9 is regulated transcriptionally and posttranslationally.
HDAC9 is known to play an essential role in regulating myocyte and adipocyte differentiation and cardiac muscle development. Also, recent studies have suggested that HDAC9 is involved in the pathogenesis of chronic diseases, including cardiovascular diseases, osteoporosis, autoimmune disease, cancer, obesity, insulin resistance, and liver fibrosis. HDAC9 modulates the expression of genes related to the pathogenesis of chronic diseases by altering chromatin structure in their promotor region or reducing the transcriptional activity of their respective transcription factors. This review summarizes the current knowledge of the regulation of HDAC9 expression and activity. Also, the roles of HDAC9 in the pathogenesis of chronic diseases are discussed, along with potential underlying mechanisms. KCI Citation Count: 22 As a member of the class IIa histone deacetylases (HDACs), HDAC9 catalyzes the deacetylation of histones and transcription factors, commonly leading to the suppression of gene transcription. The activity of HDAC9 is regulated transcriptionally and post-translationally. HDAC9 is known to play an essential role in regulating myocyte and adipocyte differentiation and cardiac muscle development. Also, recent studies have suggested that HDAC9 is involved in the pathogenesis of chronic diseases, including cardiovascular diseases, osteoporosis, autoimmune disease, cancer, obesity, insulin resistance, and liver fibrosis. HDAC9 modulates the expression of genes related to the pathogenesis of chronic diseases by altering chromatin structure in their promotor region or reducing the transcriptional activity of their respective transcription factors. This review summarizes the current knowledge of the regulation of HDAC9 expression and activity. Also, the roles of HDAC9 in the pathogenesis of chronic diseases are discussed, along with potential underlying mechanisms.As a member of the class IIa histone deacetylases (HDACs), HDAC9 catalyzes the deacetylation of histones and transcription factors, commonly leading to the suppression of gene transcription. The activity of HDAC9 is regulated transcriptionally and post-translationally. HDAC9 is known to play an essential role in regulating myocyte and adipocyte differentiation and cardiac muscle development. Also, recent studies have suggested that HDAC9 is involved in the pathogenesis of chronic diseases, including cardiovascular diseases, osteoporosis, autoimmune disease, cancer, obesity, insulin resistance, and liver fibrosis. HDAC9 modulates the expression of genes related to the pathogenesis of chronic diseases by altering chromatin structure in their promotor region or reducing the transcriptional activity of their respective transcription factors. This review summarizes the current knowledge of the regulation of HDAC9 expression and activity. Also, the roles of HDAC9 in the pathogenesis of chronic diseases are discussed, along with potential underlying mechanisms. As a member of the class IIa histone deacetylases (HDACs), HDAC9 catalyzes the deacetylation of histones and transcription factors, commonly leading to the suppression of gene transcription. The activity of HDAC9 is regulated transcriptionally and post-translationally. HDAC9 is known to play an essential role in regulating myocyte and adipocyte differentiation and cardiac muscle development. Also, recent studies have suggested that HDAC9 is involved in the pathogenesis of chronic diseases, including cardiovascular diseases, osteoporosis, autoimmune disease, cancer, obesity, insulin resistance, and liver fibrosis. HDAC9 modulates the expression of genes related to the pathogenesis of chronic diseases by altering chromatin structure in their promotor region or reducing the transcriptional activity of their respective transcription factors. This review summarizes the current knowledge of the regulation of HDAC9 expression and activity. Also, the roles of HDAC9 in the pathogenesis of chronic diseases are discussed, along with potential underlying mechanisms. |
Author | Hu, Siqi Lee, Ji-Young Cho, Eun-Hee |
AuthorAffiliation | 1 Department of Nutritional Sciences, University of Connecticut, Storrs, CT, USA 2 Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Korea |
AuthorAffiliation_xml | – name: 2 Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Korea – name: 1 Department of Nutritional Sciences, University of Connecticut, Storrs, CT, USA |
Author_xml | – sequence: 1 givenname: Siqi orcidid: 0000-0002-6171-4635 surname: Hu fullname: Hu, Siqi organization: Department of Nutritional Sciences, University of Connecticut, Storrs, CT, USA – sequence: 2 givenname: Eun-Hee surname: Cho fullname: Cho, Eun-Hee organization: Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Korea – sequence: 3 givenname: Ji-Young orcidid: 0000-0002-7945-793X surname: Lee fullname: Lee, Ji-Young organization: Department of Nutritional Sciences, University of Connecticut, Storrs, CT, USA |
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Keywords | Obesity Epigenomics Chronic disease Autoimmune diseases Cardiovascular diseases Histone deacetylases Neoplasms |
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SubjectTerms | Adipocytes - metabolism Adipocytes - pathology Amino acids Animals autoimmune diseases Autoimmune Diseases - metabolism Autoimmune Diseases - physiopathology cardiovascular diseases Cardiovascular Diseases - metabolism Cardiovascular Diseases - physiopathology Cell cycle Cell Differentiation Chronic Disease Chronic illnesses Diabetes Mellitus - metabolism Diabetes Mellitus - physiopathology Enzymes epigenomics Female Fibroblasts Genes Genomes histone deacetylases Histone Deacetylases - genetics Histones - metabolism Humans Insulin Resistance - genetics Liver cancer Liver Cirrhosis - metabolism Liver Cirrhosis - physiopathology Mice Muscle Cells - metabolism Muscle Cells - pathology Musculoskeletal system neoplasms Neoplasms - metabolism Neoplasms - physiopathology obesity Obesity - metabolism Obesity - physiopathology Osteoporosis - metabolism Osteoporosis - physiopathology Polymorphism, Single Nucleotide - genetics Promoter Regions, Genetic - genetics Proteins Regulation Repressor Proteins - genetics Review Transcription factors Transcription Factors - metabolism 내과학 |
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Title | Histone Deacetylase 9: Its Role in the Pathogenesis of Diabetes and Other Chronic Diseases |
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