Cited by 277Histone Deacetylase Inhibitors ResearchNeuroscience and Neuropharmacology ResearchMemory and Neural Mechanisms

The DOI matches its Crossref record; 118 of the 118 references it cites were found in a registry or an index.

HDAC4 Governs a Transcriptional Program Essential for Synaptic Plasticity and Memory

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Abstract

Neuronal activity influences genes involved in circuit development and information processing. However, the molecular basis of this process remains poorly understood. We found that HDAC4, a histone deacetylase that shuttles between the nucleus and cytoplasm, controls a transcriptional program essential for synaptic plasticity and memory. The nuclear import of HDAC4 and its association with chromatin is negatively regulated by NMDA receptors. In the nucleus, HDAC4 represses genes encoding constituents of central synapses, thereby affecting synaptic architecture and strength. Furthermore, we show that a truncated form of HDAC4 encoded by an allele associated with mental retardation is a gain-of-function nuclear repressor that abolishes transcription and synaptic transmission despite the loss of the deacetylase domain. Accordingly, mice carrying a mutant that mimics this allele exhibit deficits in neurotransmission, spatial learning, and memory. These studies elucidate a mechanism of experience-dependent plasticity and define the biological role of HDAC4 in the brain.

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Crossref · 10.1016/j.cell.2012.09.037

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Metadata

Authors
Sando, R., Gounko, N., Pieraut, S., Liao, L., Yates, J., & Maximov, A.
Affiliations
Scripps Research Institute (US)
Corresponding author
Maximov, Anton
Venue
Cell
Publisher
Elsevier BV
Published
2012-11
Volume
151
Issue
4
Pages
821-834
ISSN
0092-8674 (ISSN-L)
OpenAlex
W2031926951
Cited by
274
References
118
Citations by year
2026: 9 · 2025: 17 · 2024: 23 · 2023: 18 · 2022: 19 · 2021: 22 · 2020: 20 · 2019: 24 · 2018: 21 · 2017: 17 · 2016: 23 · 2015: 22 · 2014: 25 · 2013: 14
FWCI
7.85
Type
journal article
Language
en
Open access
Locations
  • Cell (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • Lirias (submittedVersion)
Funders
  • National Institute of Mental Health (MH085776, R01MH085776, R01MH067880, MH067880-09)
  • National Institute of Neurological Disorders and Stroke (P30NS057096, NS057096)
  • National Center for Research Resources (P41RR011823, RR011823)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Histone Deacetylase Inhibitors Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords
HDAC4, histone deacetylase, synaptic plasticity, memory, NMDA receptor, nuclear import, chromatin, transcriptional repression, central synapses, intellectual disability, neurotransmission, spatial learning, experience-dependent plasticity
MeSH terms
Animals, Brain, Histone Deacetylases, Memory, Neuronal Plasticity, Neurons, Synapses, Transcription Factors, Transcription, Genetic, Receptors, N-Methyl-D-Aspartate, Prosencephalon, Active Transport, Cell Nucleus, Mice

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