Evidence map›Paper›PMID 27304074›Full record

ArticleeLife2016

Enhancer regions show high histone H3.3 turnover that changes during differentiation.

Aimee M Deaton, Mariluz Gómez-Rodríguez, Jakub Mieczkowski, Michael Y Tolstorukov, Sharmistha Kundu, Ruslan I Sadreyev, Lars Et Jansen, Robert E Kingston

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

62 citing papers in PubMed, 109 citations in OpenAlex.

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  14. Multiple Roles of dXNP and dADD1-International journal of molecular sciences · 2023
    Review
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  16. Article
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2 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

8 authors at 4 institutions in 2 countries.

Aimee M DeatonDepartment of Molecular Biology, Massachusetts General Hospital, Boston, United States.
Mariluz Gómez-RodríguezLaboratory for Epigenetic Mechanisms, Instituto Gulbenkian de Ciencia, Oeiras, Portugal.
Jakub MieczkowskiDepartment of Molecular Biology, Massachusetts General Hospital, Boston, United States.
Michael Y TolstorukovDepartment of Molecular Biology, Massachusetts General Hospital, Boston, United States.
Sharmistha KunduDepartment of Molecular Biology, Massachusetts General Hospital, Boston, United States.
Ruslan I SadreyevDepartment of Molecular Biology, Massachusetts General Hospital, Boston, United States.
Lars Et JansenLaboratory for Epigenetic Mechanisms, Instituto Gulbenkian de Ciencia, Oeiras, Portugal.
Robert E KingstonDepartment of Molecular Biology, Massachusetts General Hospital, Boston, United States.ORCID 0000-0003-3628-4335
Harvard University · USInstituto Gulbenkian de Ciência · PTAmgen (United States) · USBoston University · US

Funding

Maintenance of Gene ExpressionR01GM043901 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI KINGSTON, ROBERT · 1991 to 2018
$10.7M
TRANSCRIPTION FACTOR INTERACTIONS WITH NUCLEOSOMESR01GM048405 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI KINGSTON, ROBERT · 1993 to 2008
$3.1M
NIGMS NIH HHS R01 GM043901NIGMS NIH HHS R01 GM048405
6 · The paper itself

Abstract

The organization of DNA into chromatin is dynamic; nucleosomes are frequently displaced to facilitate the ability of regulatory proteins to access specific DNA elements. To gain insight into nucleosome dynamics, and to follow how dynamics change during differentiation, we used a technique called time-ChIP to quantitatively assess histone H3.3 turnover genome-wide during differentiation of mouse ESCs. We found that, without prior assumptions, high turnover could be used to identify regions involved in gene regulation. High turnover was seen at enhancers, as observed previously, with particularly high turnover at super-enhancers. In contrast, regions associated with the repressive Polycomb-Group showed low turnover in ESCs. Turnover correlated with DNA accessibility. Upon differentiation, numerous changes in H3.3 turnover rates were observed, the majority of which occurred at enhancers. Thus, time-ChIP measurement of histone turnover shows that active enhancers are unusually dynamic in ESCs and changes in highly dynamic nucleosomes predominate at enhancers during differentiation.

Indexed as

Cell DifferentiationAnimalsChromatin ImmunoprecipitationDNAEnhancer Elements, GeneticHistonesMiceMouse Embryonic Stem CellsNucleosomesProtein BindingTime FactorsDNAHistonesNucleosomeschromatinchromosomesdifferentiationgeneshistone H3.3mousestem cellsturnover

Identifiers

PMID27304074
PMCPMC4965263
OpenAlexW2422776163

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.