Evidence map›Paper›PMID 31540912›Full record

ArticleDevelopment (Cambridge, England)2019

Distinct functions and temporal regulation of methylated histone H3 during early embryogenesis.

Beste Mutlu, Huei-Mei Chen, Silvia Gutnik, David H Hall, Sabine Keppler-Ross, Susan E Mango

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

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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 3 institutions in 2 countries.

Beste MutluDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0003-3258-0452
Huei-Mei ChenDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0002-3391-8542
Silvia GutnikBiozentrum, University of Basel, 4056 Basel, Switzerland.
David H HallCenter for C. elegans Anatomy, Albert Einstein College of Medicine, Bronx, NY 10461, USA.ORCID 0000-0001-8459-9820
Sabine Keppler-RossBiozentrum, University of Basel, 4056 Basel, Switzerland.
Susan E MangoDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA susan.mango@unibas.ch.ORCID 0000-0002-2146-3237
Harvard University · USUniversity of Basel · CHAlbert Einstein College of Medicine · US

Funding

Center for C elegans AnatomyR24OD010943 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI DAVID H. HALL, Nathan Schroeder · 2012 to 2026
$9.6M
CENTER FOR CAENORHABDITIS ELGANS ANATOMYR24RR012596 · NCRR · YESHIVA UNIVERSITY · PI HALL, DAVID H. · 1998 to 2011
$8.0M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Organogenesis of the Pharynx in C ElegansR37GM056264 · NIGMS · HARVARD UNIVERSITY · PI MANGO, SUSAN E · 2011 to 2018
$3.0M
NCRR NIH HHS R24 RR012596NIGMS NIH HHS R37 GM056264NIH HHS P40 OD010440NIH HHS R24 OD010943
6 · The paper itself

Abstract

During the first hours of embryogenesis, formation of higher-order heterochromatin coincides with the loss of developmental potential. Here, we examine the relationship between these two events, and we probe the processes that contribute to the timing of their onset. Mutations that disrupt histone H3 lysine 9 (H3K9) methyltransferases reveal that the methyltransferase MET-2 helps terminate developmental plasticity, through mono- and di-methylation of H3K9 (me1/me2), and promotes heterochromatin formation, through H3K9me3. Although loss of H3K9me3 perturbs formation of higher-order heterochromatin, embryos are still able to terminate plasticity, indicating that the two processes can be uncoupled. Methylated H3K9 appears gradually in developing

Indexed as

Embryonic DevelopmentAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell CountEmbryo, NonmammalianGastrulationHeterochromatinHistonesInterphaseMethylationRNA Polymerase IIS PhaseTime FactorsTranscription, GeneticCaenorhabditis elegans ProteinsHeterochromatinHistonesRNA Polymerase IIEmbryogenesisHeterochromatinmet-2PluripotencySETDB1

Identifiers

PMID31540912
PMCPMC6803369
OpenAlexW2973237198

What OpenQuestion holds

Textmetadata
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.