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Accurate Recycling of Parental Histones Reproduces the Histone Modification Landscape during DNA Replication.

Molecular cell (2018-08-28)
Nazaret Reverón-Gómez, Cristina González-Aguilera, Kathleen R Stewart-Morgan, Nataliya Petryk, Valentin Flury, Simona Graziano, Jens Vilstrup Johansen, Janus Schou Jakobsen, Constance Alabert, Anja Groth
ABSTRACT

Chromatin organization is disrupted genome-wide during DNA replication. On newly synthesized DNA, nucleosomes are assembled from new naive histones and old modified histones. It remains unknown whether the landscape of histone post-translational modifications (PTMs) is faithfully copied during DNA replication or the epigenome is perturbed. Here we develop chromatin occupancy after replication (ChOR-seq) to determine histone PTM occupancy immediately after DNA replication and across the cell cycle. We show that H3K4me3, H3K36me3, H3K79me3, and H3K27me3 positional information is reproduced with high accuracy on newly synthesized DNA through histone recycling. Quantitative ChOR-seq reveals that de novo methylation to restore H3K4me3 and H3K27me3 levels occurs across the cell cycle with mark- and locus-specific kinetics. Collectively, this demonstrates that accurate parental histone recycling preserves positional information and allows PTM transmission to daughter cells while modification of new histones gives rise to complex epigenome fluctuations across the cell cycle that could underlie cell-to-cell heterogeneity.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Aminoguanidine hydrochloride, ≥98%
Sigma-Aldrich
Tris(3-hydroxypropyltriazolylmethyl)amine, 95%
Sigma-Aldrich
Biotin, ≥99% (HPLC), lyophilized powder