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The BAF complex enhances transcription through interaction with H3K56ac in the histone globular domain.
- Source :
-
Nature communications [Nat Commun] 2024 Nov 07; Vol. 15 (1), pp. 9614. Date of Electronic Publication: 2024 Nov 07. - Publication Year :
- 2024
-
Abstract
- Histone post-translational modifications play pivotal roles in eukaryotic gene expression. To date, most studies have focused on modifications in unstructured histone N-terminal tail domains and their binding proteins. However, transcriptional regulation by chromatin-effector proteins that directly recognize modifications in histone globular domains has yet to be clearly demonstrated, despite the richness of their multiple modifications. Here, we show that the ATP-dependent chromatin-remodeling BAF complex stimulates p53-dependent transcription through direct interaction with H3K56ac located on the lateral surface of the histone globular domain. Mechanistically, the BAF complex recognizes nucleosomal H3K56ac via the DPF domain in the DPF2 subunit and exhibits enhanced nucleosome-remodeling activity in the presence of H3K56ac. We further demonstrate that a defect in H3K56ac-BAF complex interaction leads to impaired p53-dependent gene expression and DNA damage responses. Our study provides direct evidence that histone globular domain modifications participate in the regulation of gene expression.<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Transcription, Genetic
Nucleosomes metabolism
Acetylation
Protein Domains
Protein Binding
DNA Damage
Transcription Factors metabolism
Transcription Factors genetics
Protein Processing, Post-Translational
HEK293 Cells
Gene Expression Regulation
Histones metabolism
Histones genetics
Tumor Suppressor Protein p53 metabolism
Tumor Suppressor Protein p53 genetics
Tumor Suppressor Protein p53 chemistry
DNA-Binding Proteins metabolism
DNA-Binding Proteins genetics
DNA-Binding Proteins chemistry
Chromatin Assembly and Disassembly
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 15
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 39511190
- Full Text :
- https://doi.org/10.1038/s41467-024-53981-0