Evidence map›Paper›PMID 29995890›Full record

ArticlePLoS genetics2018

Cyclin G and the Polycomb Repressive complexes PRC1 and PR-DUB cooperate for developmental stability.

Delphine Dardalhon-Cuménal, Jérôme Deraze, Camille A Dupont, Valérie Ribeiro, Anne Coléno-Costes, Juliette Pouch, Stéphane Le Crom, Hélène Thomassin, Vincent Debat, Neel B Randsholt and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  5. Review
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

11 authors at 1 institution in 1 country.

Delphine Dardalhon-CuménalSorbonne Université, Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Paris-Seine (IBPS), Laboratory of Developmental Biology (LBD), Paris, France.
Jérôme DerazeSorbonne Université, Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Paris-Seine (IBPS), Laboratory of Developmental Biology (LBD), Paris, France.
Camille A DupontSorbonne Université, Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Paris-Seine (IBPS), Laboratory of Developmental Biology (LBD), Paris, France.
Valérie RibeiroSorbonne Université, Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Paris-Seine (IBPS), Laboratory of Developmental Biology (LBD), Paris, France.
Anne Coléno-CostesSorbonne Université, Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Paris-Seine (IBPS), Laboratory of Developmental Biology (LBD), Paris, France.
Juliette PouchInstitut de biologie de l'Ecole normale supérieure (IBENS), Ecole normale supérieure, CNRS, INSERM, PSL Université Paris Paris, France.
Stéphane Le CromInstitut de biologie de l'Ecole normale supérieure (IBENS), Ecole normale supérieure, CNRS, INSERM, PSL Université Paris Paris, France.ORCID 0000-0002-0534-7797
Hélène ThomassinSorbonne Université, Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Paris-Seine (IBPS), Laboratory of Developmental Biology (LBD), Paris, France.
Vincent DebatInstitut de Systematique, Evolution, Biodiversité ISYEB UMR 7205, MNHN, CNRS, Sorbonne Université, EPHE, Muséum national d'Histoire naturelle, Sorbonne Universités, Paris, France.ORCID 0000-0003-0040-1181
Neel B RandsholtSorbonne Université, Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Paris-Seine (IBPS), Laboratory of Developmental Biology (LBD), Paris, France.
Frédérique PeronnetSorbonne Université, Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Paris-Seine (IBPS), Laboratory of Developmental Biology (LBD), Paris, France.ORCID 0000-0003-1354-240X
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In Drosophila, ubiquitous expression of a short Cyclin G isoform generates extreme developmental noise estimated by fluctuating asymmetry (FA), providing a model to tackle developmental stability. This transcriptional cyclin interacts with chromatin regulators of the Enhancer of Trithorax and Polycomb (ETP) and Polycomb families. This led us to investigate the importance of these interactions in developmental stability. Deregulation of Cyclin G highlights an organ intrinsic control of developmental noise, linked to the ETP-interacting domain, and enhanced by mutations in genes encoding members of the Polycomb Repressive complexes PRC1 and PR-DUB. Deep-sequencing of wing imaginal discs deregulating CycG reveals that high developmental noise correlates with up-regulation of genes involved in translation and down-regulation of genes involved in energy production. Most Cyclin G direct transcriptional targets are also direct targets of PRC1 and RNAPolII in the developing wing. Altogether, our results suggest that Cyclin G, PRC1 and PR-DUB cooperate for developmental stability.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsAnimals, Genetically ModifiedCell NucleusChromatinCyclin GDown-RegulationDrosophila melanogasterDrosophila ProteinsFemaleGene Regulatory NetworksMalePolycomb Repressive Complex 1Protein BindingUp-RegulationWings, AnimalChromatinCyclin GDrosophila ProteinsPolycomb Repressive Complex 1

Identifiers

PMID29995890
PMCPMC6065198
OpenAlexW2951321515

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.