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Gene-Specific H1 Eviction through a Transcriptional Activator→p300→NAP1→H1 Pathway.
- Source :
-
Molecular cell [Mol Cell] 2019 Apr 18; Vol. 74 (2), pp. 268-283.e5. Date of Electronic Publication: 2019 Mar 19. - Publication Year :
- 2019
-
Abstract
- Linker histone H1 has been correlated with transcriptional inhibition, but the mechanistic basis of the inhibition and its reversal during gene activation has remained enigmatic. We report that H1-compacted chromatin, reconstituted in vitro, blocks transcription by abrogating core histone modifications by p300 but not activator and p300 binding. Transcription from H1-bound chromatin is elicited by the H1 chaperone NAP1, which is recruited in a gene-specific manner through direct interactions with activator-bound p300 that facilitate core histone acetylation (by p300) and concomitant eviction of H1 and H2A-H2B. An analysis in B cells confirms the strong dependency on NAP1-mediated H1 eviction for induction of the silent CD40 gene and further demonstrates that H1 eviction, seeded by activator-p300-NAP1-H1 interactions, is propagated over a CCCTC-binding factor (CTCF)-demarcated region through a distinct mechanism that also involves NAP1. Our results confirm direct transcriptional inhibition by H1 and establish a gene-specific H1 eviction mechanism through an activator→p300→NAP1→H1 pathway.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)
- Subjects :
- Acetylation
B-Lymphocytes chemistry
Binding Sites
CCCTC-Binding Factor chemistry
CD40 Antigens genetics
Chromatin chemistry
Chromatin genetics
E1A-Associated p300 Protein chemistry
Histone Code
Histones chemistry
Histones genetics
Humans
Molecular Chaperones chemistry
Molecular Chaperones genetics
Nucleosomes chemistry
Nucleosomes genetics
Promoter Regions, Genetic
Protein Binding genetics
Proteins chemistry
tRNA Methyltransferases
CCCTC-Binding Factor genetics
E1A-Associated p300 Protein genetics
Proteins genetics
Transcription, Genetic
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4164
- Volume :
- 74
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Molecular cell
- Publication Type :
- Academic Journal
- Accession number :
- 30902546
- Full Text :
- https://doi.org/10.1016/j.molcel.2019.02.016