Evidence map›Paper›PMID 26759081›Full record

ArticleNature communications2016

Chromatin topology is coupled to Polycomb group protein subnuclear organization.

Ajazul H Wani, Alistair N Boettiger, Patrick Schorderet, Ayla Ergun, Christine Münger, Ruslan I Sadreyev, Xiaowei Zhuang, Robert E Kingston, Nicole J Francis

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
15.1field-weighted citation impact, top 1% 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

111 citing papers in PubMed, 208 citations in OpenAlex.

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51 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

9 authors at 4 institutions in 2 countries.

Ajazul H WaniDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Alistair N BoettigerHoward Hughes Medical Institute, Harvard University Cambridge, Cambridge, Massachusetts 02138, USA.
Patrick SchorderetDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Ayla ErgunDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Christine MüngerInstitut de recherches cliniques de Montréal, Montréal, Québec, Canada.
Ruslan I SadreyevDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Xiaowei ZhuangHoward Hughes Medical Institute, Harvard University Cambridge, Cambridge, Massachusetts 02138, USA.
Robert E KingstonDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Nicole J FrancisInstitut de recherches cliniques de Montréal, Montréal, Québec, Canada.
Harvard University · USMassachusetts General Hospital · USMontreal Clinical Research Institute · CAHoward Hughes Medical Institute · US

Funding

ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CHRISTOPHER P DUGGAN · 1994 to 2026
$31.6M
Maintenance of Gene ExpressionR01GM043901 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI KINGSTON, ROBERT · 1991 to 2018
$10.7M
Canadian Institutes of Health ResearchHoward Hughes Medical InstituteNIDDK NIH HHS P30 DK040561NIGMS NIH HHS R01 GM043901
6 · The paper itself

Abstract

The genomes of metazoa are organized at multiple scales. Many proteins that regulate genome architecture, including Polycomb group (PcG) proteins, form subnuclear structures. Deciphering mechanistic links between protein organization and chromatin architecture requires precise description and mechanistic perturbations of both. Using super-resolution microscopy, here we show that PcG proteins are organized into hundreds of nanoscale protein clusters. We manipulated PcG clusters by disrupting the polymerization activity of the sterile alpha motif (SAM) of the PcG protein Polyhomeotic (Ph) or by increasing Ph levels. Ph with mutant SAM disrupts clustering of endogenous PcG complexes and chromatin interactions while elevating Ph level increases cluster number and chromatin interactions. These effects can be captured by molecular simulations based on a previously described chromatin polymer model. Both perturbations also alter gene expression. Organization of PcG proteins into small, abundant clusters on chromatin through Ph SAM polymerization activity may shape genome architecture through chromatin interactions.

Indexed as

Amino Acid MotifsAnimalsCell LineChromatinChromatin ImmunoprecipitationDNA-Binding ProteinsDrosophilaDrosophila ProteinsFluorescent Antibody TechniqueIntranuclear SpaceMicroscopyMolecular Dynamics SimulationOptical ImagingPolycomb-Group ProteinsPolycomb Repressive Complex 1PolymersChromatinDNA-Binding ProteinsDrosophila Proteinsph-d protein, DrosophilaPolycomb-Group ProteinsPolycomb Repressive Complex 1Polymers

Identifiers

PMID26759081
PMCPMC4735512
OpenAlexW2233967916

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.