| Literature DB >> 30902546 |
Miho Shimada1, Wei-Yi Chen2, Tomoyoshi Nakadai1, Takashi Onikubo1, Mohamed Guermah1, Daniela Rhodes3, Robert G Roeder4.
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.Entities:
Keywords: B cell maturation; CTCF; NAP1; NF-κB; higher-order chromatin; in vitro transcription; linker histone; p300; transcription
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Year: 2019 PMID: 30902546 PMCID: PMC6598686 DOI: 10.1016/j.molcel.2019.02.016
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970