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Gene-Specific H1 Eviction through a Transcriptional Activator?p300?NAP1?H1 Pathway.


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.

SUBMITTER: Shimada M 

PROVIDER: S-EPMC6598686 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature

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Gene-Specific H1 Eviction through a Transcriptional Activator→p300→NAP1→H1 Pathway.

Shimada Miho M   Chen Wei-Yi WY   Nakadai Tomoyoshi T   Onikubo Takashi T   Guermah Mohamed M   Rhodes Daniela D   Roeder Robert G RG  

Molecular cell 20190319 2


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 wit  ...[more]

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