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Quantification of parental and new histones H3, H4 and H2A by mass spectrometry: analysis of their dynamics along cell cycle progression in WT and MCM2-2A mutant mouse ESCs

ABSTRACT: During DNA replication parental, nucleosomic histones are segregated almost symmetrically to the two daughter DNA strands enabling mitotic inheritance of histones and their PTMs. In MCM2 histone-binding mutant ESCs (MCM2-2A), histones are recycled asymmetrically to the leading strand. To evaluate if loss of parental histones contributes to the asymmetry, we tracked new and old histones quantitatively by pulse-Triple-SILAC-MS. The quantification showed no change in dilution and incorporation dynamics in MCM2-2A cells, demonstrating that parental histones are not lost at replication forks but re-routed from the lagging to the leading strand.

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Embryo, Embryonic Stem Cell

SUBMITTER: Victor Solis

LAB HEAD: Anja Groh

PROVIDER: PXD030364 | Pride | 2023-08-30

REPOSITORIES: Pride

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			Action	DRS
	H3H4H2A-quant-triple-SILAC_Raw-intensities_PRIDE.xlsx	Xlsx
	Ref_xxx_AWE1_10_Mut1_120619.raw	Raw
	Ref_xxx_AWE1_11_Mut1_120619.raw	Raw
	Ref_xxx_AWE1_12_Mut1_120619.raw	Raw
	Ref_xxx_AWE1_13_Mut1_120619.raw	Raw

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