Cited by 389Histone Deacetylase Inhibitors ResearchGenomics and Chromatin DynamicsEpigenetics and DNA Methylation

NuRD and SIN3

Ahringer, Julie·2000·Trends in Genetics

Abstract

Transcription repression mediated through histone deacetylase (HDAC) complexes is widespread, and mechanisms by which HDAC complexes act have been revealed by extensive studies in vitro and in cell culture. However, until recently, little has been known about the developmental roles of histone deacetylation. Mutants now exist for a number of members of the two major HDAC complexes (NuRD and SIN3) and some associated proteins. The emerging picture is that these complexes have specific functions in development, rather than being required for most cellular processes.

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Crossref · 10.1016/s0168-9525(00)02066-7

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Authors
Ahringer, J.
Affiliations
Wellcome Trust (GB)
Corresponding author
Ahringer, Julie
Venue
Trends in Genetics
Publisher
Elsevier BV
Published
2000-08
Volume
16
Issue
8
Pages
351-356
ISSN
0168-9525 (ISSN-L)
OpenAlex
W2027297574
Cited by
388
References
63
Citations by year
2026: 8 · 2025: 5 · 2024: 2 · 2023: 5 · 2022: 5 · 2021: 4 · 2020: 7 · 2019: 8 · 2018: 4 · 2017: 11 · 2016: 8 · 2015: 13 · 2014: 15 · 2013: 16 · 2012: 16
FWCI
2.42
Type
journal article
Language
en
Open access
closed
Locations
  • Trends in Genetics (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Wellcome Trust (054523)
  • Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
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
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
Keywords
NuRD complex, histone deacetylase complex, transcriptional repression, histone deacetylation, developmental gene regulation, chromatin regulation
MeSH terms
Animals, Histone Deacetylases, Humans, Models, Biological, Receptors, Cell Surface, Transcription, Genetic, Arabidopsis, ras Proteins, Macromolecular Substances, Mi-2 Nucleosome Remodeling and Deacetylase Complex, Sin3 Histone Deacetylase and Corepressor Complex

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