Post-translational Modifications Regulate Class IIa Histone Deacetylase (HDAC) Function in Health and Disease
Open accessAbstract
Class IIa histone deacetylases (HDACs4, -5, -7, and -9) modulate the physiology of the human cardiovascular, musculoskeletal, nervous, and immune systems. The regulatory capacity of this family of enzymes stems from their ability to shuttle between nuclear and cytoplasmic compartments in response to signal-driven post-translational modification. Here, we review the current knowledge of modifications that control spatial and temporal histone deacetylase functions by regulating subcellular localization, transcriptional functions, and cell cycle-dependent activity, ultimately impacting on human disease. We discuss the contribution of these modifications to cardiac and vascular hypertrophy, myoblast differentiation, neuronal cell survival, and neurodegenerative disorders.
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HDAC4 shuttles between the cell nucleus and cytoplasm.
“It shuttles between the cell nucleus and cytoplasm.140”
From Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential (2023) · cites this paper as [140]
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BindingDB Entry 50008262: Recent advances in class IIa histone deacetylases research.
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- Authors
- Mathias, R. A., Guise, A. J., & Cristea, I. M.
- Affiliations
- La Trobe University (AU)
- Princeton University (US)
- Venue
- Molecular & Cellular Proteomics
- Publisher
- Elsevier BV
- Published
- 2015-03
- Volume
- 14
- Issue
- 3
- Pages
- 456-470
- ISSN
- 1535-9476 (ISSN-L)
- PMC
- PMC4349969
- OpenAlex
- W2128449069
- Cited by
- 93
- References
- 169
- Citations by year
- 2026: 4 · 2025: 10 · 2024: 11 · 2023: 7 · 2022: 8 · 2021: 10 · 2020: 11 · 2019: 12 · 2018: 5 · 2017: 6 · 2016: 8 · 2015: 1
- FWCI
- 0.65
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Molecular & Cellular Proteomics (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (DP1DA026192, R21AI102187, R21HD073044)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Histone Deacetylase Inhibitors Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Keywords
- class IIa histone deacetylases, HDAC4, HDAC5, HDAC7, HDAC9, post-translational modification, subcellular localization, nucleocytoplasmic shuttling, transcriptional regulation, cell cycle regulation, cardiac hypertrophy, vascular hypertrophy, myogenesis, neuronal survival, neurodegenerative diseases
- MeSH terms
- Histone Deacetylases, Humans, Neurons, Osteogenesis, Protein Processing, Post-Translational, Repressor Proteins, Muscle Development
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