Evidence map›Paper›PMID 31675501›Full record

ArticleCell2019

Active and Repressed Chromatin Domains Exhibit Distinct Nucleosome Segregation during DNA Replication.

Thelma M Escobar, Ozgur Oksuz, Ricardo Saldaña-Meyer, Nicolas Descostes, Roberto Bonasio, Danny Reinberg

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
8.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

117 citing papers in PubMed, 173 citations in OpenAlex.

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  14. Constraints and tunability of antigen-agnostic memory durability.bioRxiv : the preprint server for biology · 2025
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57 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Thelma M EscobarHoward Hughes Medical Institute, New York University Langone Medical Center, New York, NY 10016, USA; New York University Langone Medical Center, New York, NY 10016, USA.
Ozgur OksuzHoward Hughes Medical Institute, New York University Langone Medical Center, New York, NY 10016, USA; New York University Langone Medical Center, New York, NY 10016, USA.
Ricardo Saldaña-MeyerHoward Hughes Medical Institute, New York University Langone Medical Center, New York, NY 10016, USA; New York University Langone Medical Center, New York, NY 10016, USA.
Nicolas DescostesHoward Hughes Medical Institute, New York University Langone Medical Center, New York, NY 10016, USA; New York University Langone Medical Center, New York, NY 10016, USA.
Roberto BonasioHoward Hughes Medical Institute, New York University Langone Medical Center, New York, NY 10016, USA; New York University Langone Medical Center, New York, NY 10016, USA.
Danny ReinbergHoward Hughes Medical Institute, New York University Langone Medical Center, New York, NY 10016, USA; New York University Langone Medical Center, New York, NY 10016, USA. Electronic address: danny.reinberg@nyumc.org.
Howard Hughes Medical Institute · USNYU Langone Health · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Repression via Facultative HeterochromatinR01CA199652 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI REINBERG, DANNY · 2015 to 2025
$4.2M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA016087NCI NIH HHS R01 CA199652
6 · The paper itself

Abstract

Chromatin domains and their associated structures must be faithfully inherited through cellular division to maintain cellular identity. However, accessing the localized strategies preserving chromatin domain inheritance, specifically the transfer of parental, pre-existing nucleosomes with their associated post-translational modifications (PTMs) during DNA replication, is challenging in living cells. We devised an inducible, proximity-dependent labeling system to irreversibly mark replication-dependent H3.1 and H3.2 histone-containing nucleosomes at desired loci in mouse embryonic stem cells so that their fate after DNA replication could be followed. Strikingly, repressed chromatin domains are preserved through local re-deposition of parental nucleosomes. In contrast, nucleosomes decorating active chromatin domains do not exhibit such preservation. Notably, altering cell fate leads to an adjustment of the positional inheritance of parental nucleosomes that reflects the corresponding changes in chromatin structure. These findings point to important mechanisms that contribute to parental nucleosome segregation to preserve cellular identity.

Indexed as

Epigenesis, GeneticAnimalsCell DifferentiationCell DivisionCell LineageChromatinChromatin Assembly and DisassemblyDNA ReplicationHistonesMiceMouse Embryonic Stem CellsNucleosomesProtein Processing, Post-TranslationalChromatinHistonesNucleosomesDNA replicationepigeneticgene expressiongene silencingparental nucleosome segregationpolycombpost-translational histone modificationsrepressed chromatin domains

Identifiers

PMID31675501
PMCPMC6917041
OpenAlexW2989300252

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.