Evidence map›Paper›PMID 27181215›Full record

ArticleScientific reports2016

Polycomb repressive complex 1 controls uterine decidualization.

Fenghua Bian, Fei Gao, Andrey V Kartashov, Anil G Jegga, Artem Barski, Sanjoy K Das

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Epigenetic control of embryo-uterine crosstalk at peri-implantation.Cellular and molecular life sciences : CMLS · 2019
    Review
  13. Article
  14. TGFβ superfamily signaling and uterine decidualization.Reproductive biology and endocrinology : RB&E · 2017
    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

6 authors at 2 institutions in 1 country.

Fenghua BianDivision of Reproductive Sciences, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Fei GaoDivision of Reproductive Sciences, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Andrey V KartashovDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 49267, USA.
Anil G JeggaDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 49267, USA.
Artem BarskiDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 49267, USA.
Sanjoy K DasDivision of Reproductive Sciences, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
University of Cincinnati Medical Center · USCincinnati Children's Hospital Medical Center · US

Funding

LCenter for Clinical and Translational Science and TrainingUL1TR001425 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., KISSELA, BRETT M · 2015 to 2024
$37.5M
ENVIRONMENTAL TOXINS AND UTERINE GENE EXPRESSIONR01ES007814 · NIEHS · VANDERBILT UNIVERSITY · PI DAS, SANJOY K. · 1997 to 2012
$3.2M
Direct Epigenetic Reprogramming of T CellsDP2GM119134 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI BARSKI, ARTEM · 2015 to 2015
$2.3M
Molecular Signaling in DecidualizationR01HD056044 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI DAS, SANJOY K. · 2009 to 2010
$1.1M
NCATS NIH HHS UL1 TR001425NICHD NIH HHS R01 HD056044NIEHS NIH HHS R01 ES007814NIGMS NIH HHS DP2 GM119134
6 · The paper itself

Abstract

Uterine stromal cell decidualization is an essential part of the reproductive process. Decidual tissue development requires a highly regulated control of the extracellular tissue remodeling; however the mechanism of this regulation remains unknown. Through systematic expression studies, we detected that Cbx4/2, Rybp, and Ring1B [components of polycomb repressive complex 1 (PRC1)] are predominantly utilized in antimesometrial decidualization with polyploidy. Immunofluorescence analyses revealed that PRC1 members are co-localized with its functional histone modifier H2AK119ub1 (mono ubiquitination of histone-H2A at lysine-119) in polyploid cell. A potent small-molecule inhibitor of Ring1A/B E3-ubiquitin ligase or siRNA-mediated suppression of Cbx4 caused inhibition of H2AK119ub1, in conjunction with perturbation of decidualization and polyploidy development, suggesting a role for Cbx4/Ring1B-containing PRC1 in these processes. Analyses of genetic signatures by RNA-seq studies showed that the inhibition of PRC1 function affects 238 genes (154 up and 84 down) during decidualization. Functional enrichment analyses identified that about 38% genes primarily involved in extracellular processes are specifically targeted by PRC1. Furthermore, ~15% of upregulated genes exhibited a significant overlap with the upregulated Bmp2 null-induced genes in mice. Overall, Cbx4/Ring1B-containing PRC1 controls decidualization via regulation of extracellular gene remodeling functions and sheds new insights into underlying molecular mechanism(s) through transcriptional repression regulation.

Indexed as

AnimalsBone Morphogenetic Protein 2Cells, CulturedDeciduaEpigenetic RepressionFemaleGene Expression RegulationHistonesLigasesMaleMiceMice, KnockoutPolycomb-Group ProteinsPolycomb Repressive Complex 1PolyploidyRepressor ProteinsBmp2 protein, mouseBone Morphogenetic Protein 2Cbx4 protein, mouseHistonesLigasesPolycomb-Group ProteinsPolycomb Repressive Complex 1Repressor ProteinsRNA, Small InterferingRnf2 protein, mouseRybp protein, mouseUbiquitin-Protein Ligases

Identifiers

PMID27181215
PMCPMC4867636
OpenAlexW2406679970

What OpenQuestion holds

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LicenceCC BY
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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.