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HDAC1 and HDAC3 underlie dynamic H3K9 acetylation during embryonic neurogenesis and in schizophrenia-like animals
J. Večeřa, E. Bártová, J. Krejčí, S. Legartová, D. Komůrková, J. Rudá-Kučerová, T. Štark, E. Dražanová, T. Kašpárek, A. Šulcová, FJ. Dekker, W. Szymanski, C. Seiser, G. Weitzer, R. Mechoulam, V. Micale, S. Kozubek,
Language English Country United States
Document type Journal Article
PubMed
28300292
DOI
10.1002/jcp.25914
Knihovny.cz E-resources
- MeSH
- Acetylation MeSH
- Cannabinoid Receptor Antagonists pharmacology MeSH
- Antipsychotic Agents pharmacology MeSH
- Time Factors MeSH
- Epigenesis, Genetic MeSH
- Gestational Age MeSH
- Histone Deacetylase 1 antagonists & inhibitors genetics metabolism MeSH
- Histone Deacetylases genetics metabolism MeSH
- Histones metabolism MeSH
- Histone Deacetylase Inhibitors pharmacology MeSH
- Methylazoxymethanol Acetate MeSH
- Disease Models, Animal MeSH
- Neural Cell Adhesion Molecules genetics metabolism MeSH
- Brain drug effects embryology enzymology pathology MeSH
- Mice, Inbred C57BL MeSH
- Neurogenesis * drug effects MeSH
- Neurons drug effects enzymology pathology MeSH
- Protein Processing, Post-Translational MeSH
- Rats, Sprague-Dawley MeSH
- Receptor, Cannabinoid, CB1 antagonists & inhibitors metabolism MeSH
- Schizophrenia chemically induced drug therapy enzymology genetics MeSH
- Signal Transduction MeSH
- SOXB1 Transcription Factors genetics metabolism MeSH
- Gene Expression Regulation, Developmental MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
Although histone acetylation is one of the most widely studied epigenetic modifications, there is still a lack of information regarding how the acetylome is regulated during brain development and pathophysiological processes. We demonstrate that the embryonic brain (E15) is characterized by an increase in H3K9 acetylation as well as decreases in the levels of HDAC1 and HDAC3. Moreover, experimental induction of H3K9 hyperacetylation led to the overexpression of NCAM in the embryonic cortex and depletion of Sox2 in the subventricular ependyma, which mimicked the differentiation processes. Inducing differentiation in HDAC1-deficient mouse ESCs resulted in early H3K9 deacetylation, Sox2 downregulation, and enhanced astrogliogenesis, whereas neuro-differentiation was almost suppressed. Neuro-differentiation of (wt) ESCs was characterized by H3K9 hyperacetylation that was associated with HDAC1 and HDAC3 depletion. Conversely, the hippocampi of schizophrenia-like animals showed H3K9 deacetylation that was regulated by an increase in both HDAC1 and HDAC3. The hippocampi of schizophrenia-like brains that were treated with the cannabinoid receptor-1 inverse antagonist AM251 expressed H3K9ac at the level observed in normal brains. Together, the results indicate that co-regulation of H3K9ac by HDAC1 and HDAC3 is important to both embryonic brain development and neuro-differentiation as well as the pathophysiology of a schizophrenia-like phenotype.
Chemical and Pharmaceutical Biology University of Groningen Groningen The Netherlands
Faculty of Medicine Department of Pharmacology Masaryk University Brno Czech Republic
Faculty of Medicine Institute for Drug Research Hebrew University of Jerusalem Jerusalem Israel
Faculty of Science Department of Experimental Biology Masaryk University Brno Czech Republic
Institute of Biophysics of the Czech Academy of Sciences v v i Brno Czech Republic
References provided by Crossref.org
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