Abstract
Recent advances highlight two important chromatin remodeling systems involved in the transcriptional process. One system includes several members of the evolutionarily conserved SWI2/SNF2 family found in distinct multiprotein complexes with ATP-dependent nucleosome destabilizing activity; the other is the enzymatic system that governs histone acetylation and deacetylation. Identification of the catalytic subunits of these opposing histone-modifying activities reveal conserved proteins defined genetically as transcriptional regulators.
MeSH Terms
Acetylation
Acetyltransferases
Adenosine Triphosphate
Animals
Cell Cycle Proteins/metabolism
Chromatin
DNA/chemistry
DNA Helicases
DNA-Binding Proteins/metabolism
Fungal Proteins/metabolism
Histone Acetyltransferases
Histone Deacetylases/metabolism
Histones
Humans
Nuclear Proteins/metabolism
Nucleic Acid Conformation
Nucleosomes
Protein Kinases/metabolism
Saccharomyces cerevisiae Proteins
TATA-Binding Protein Associated Factors
Tetrahymena
Transcription Factor TFIID
Transcription Factors/metabolism
Transcription, Genetic
p300-CBP Transcription Factors
Chemicals
CHD1 protein, S cerevisiae
Cell Cycle Proteins
Chromatin
DNA-Binding Proteins
Fungal Proteins
Histones
Nuclear Proteins
Nucleosomes
SMARCA1 protein, human
SMARCA2 protein, human
Saccharomyces cerevisiae Proteins
TATA-Binding Protein Associated Factors
Transcription Factor TFIID
Transcription Factors
Adenosine Triphosphate
DNA
Acetyltransferases
Histone Acetyltransferases
p300-CBP Transcription Factors
p300-CBP-associated factor
Protein Kinases
TATA-binding protein associated factor 250 kDa
Histone Deacetylases
SMARCA4 protein, human
DNA Helicases
CHD1 protein, human
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tsukiyama T
Laboratory of Molecular Cell Biology, National Cancer Institute, National Institutes of Health, Building 37, Room 5E-26, Bethesda, Maryland, 20892-4255, USA.
Wu C