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Histone dynamics at replication forks in embryonic stem cells

ABSTRACT: We employ inducible mutants to dissect the early and late consequences of impaired histone recycling. We find rapid accumulation of H3K27me3 in response to impaired histone recycling, preceding gene expression changes. Simultaneous disruption of both leading (POLE4) and lagging strand (MCM2-2A) recycling pathways impairs transmission of parental histones to new DNA, with release of parental histones to the soluble pool. This loss of histone inheritance alters gene expression in embryonic stem cells, challenges differentiation programs and compromises cell viability. Our findings demonstrate the importance of efficient transmission of histone-based information during DNA replication for maintaining chromatin landscapes, differentiation potential, and cellular viability.

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Embryonic Stem Cell

DISEASE(S): Acute Leukemia

SUBMITTER: Moritz Voelker-Albert

LAB HEAD: Anja Groth

PROVIDER: PXD053300 | Pride | 2025-01-12

REPOSITORIES: pride

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			Action	DRS
	20201228_MVA_Screen1_8.tif	Other
	20201228_MVA_screen9_16.tif	Other
	Peptide_Ratio_Results_wH33_050121.csv	Csv
	RefXXX_BRIC_LKO_555_H11_DMSO_MS1_181220.raw	Raw
	RefXXX_BRIC_LKO_555_H11_DMSO_MS2_181220.raw	Raw

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