Evidence map›Paper›PMID 12628927›Full record

ArticleThe EMBO journal2003

Transcription factor YY1 functions as a PcG protein in vivo.

Lakshmi Atchison, Ayesha Ghias, Frank Wilkinson, Nancy Bonini, Michael L Atchison

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

115 citing papers in PubMed, 208 citations in OpenAlex.

  1. Review
  2. Article
  3. The YYR (YY1- RKIP) Regulatory Axis in the pathogenesis of Cancer and Immune Evasion.Journal of experimental & clinical cancer research : CR · 2025
    Review
  4. Article
  5. Article
  6. Yin Yang 1: Function, Mechanisms, and Glia.Neurochemical research · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Dual Role of YY1 in HPV Life Cycle and Cervical Cancer Development.International journal of molecular sciences · 2022
    Review
  19. Article
  20. Article

55 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

5 authors at 1 institution in 1 country.

Lakshmi AtchisonDepartment of Biology, Chestnut Hill College, 9601 Germantown Avenue, Philadelphia, PA 19118, USA. atchison@vet.upenn.edu
Ayesha Ghias
Frank Wilkinson
Nancy Bonini
Michael L Atchison
Chestnut Hill College · US

Funding

DEVELOPMENTAL CONTROL OF IMMUNOGLOBULIN TRANSCRIPTIONR01GM042415 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI ATCHISON, MICHAEL L. · 1989 to 2005
$1.7M
PHYSICIAN AND SCIENTIST TRAINING IN UROLOGICAL RESEARCHT32DK007708 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI WEIN, ALAN J · 1993 to 2007
$1.0M
MOLECULAR CONTROL OF CELL SURVIVAL IN EYE DEVELOPMENTR29EY011259 · NEI · UNIVERSITY OF PENNSYLVANIA · PI BONINI, NANCY M · 1996 to 2000
$102k
NEI NIH HHS R29-EY11259NIDDK NIH HHS T32 DK007708NIDDK NIH HHS T32 DK07708NIGMS NIH HHS R01 GM042415
6 · The paper itself

Abstract

Polycomb group (PcG) proteins function as high molecular weight complexes that maintain transcriptional repression patterns during embryogenesis. The vertebrate DNA binding protein and transcriptional repressor, YY1, shows sequence homology with the Drosophila PcG protein, pleiohomeotic (PHO). YY1 might therefore be a vertebrate PcG protein. We used Drosophila embryo and larval/imaginal disc transcriptional repression systems to determine whether YY1 repressed transcription in a manner consistent with PcG function in vivo. YY1 repressed transcription in Drosophila, and this repression was stable on a PcG-responsive promoter, but not on a PcG-non-responsive promoter. PcG mutants ablated YY1 repression, and YY1 could substitute for PHO in repressing transcription in wing imaginal discs. YY1 functionally compensated for loss of PHO in pho mutant flies and partially corrected mutant phenotypes. Taken together, these results indicate that YY1 functions as a PcG protein. Finally, we found that YY1, as well as Polycomb, required the co-repressor protein CtBP for repression in vivo. These results provide a mechanism for recruitment of vertebrate PcG complexes to DNA and demonstrate new functions for YY1.

Indexed as

Alcohol OxidoreductasesAnimalsDNA-Binding ProteinsDrosophilaDrosophila ProteinsEmbryo, NonmammalianErythroid-Specific DNA-Binding FactorsGene Expression Regulation, DevelopmentalGenes, InsectGenes, ReporterHomeodomain ProteinsLarvaModels, BiologicalMutationPhenotypePhosphoproteinsAlcohol OxidoreductasesC-terminal binding proteinDNA-Binding ProteinsDrosophila ProteinsErythroid-Specific DNA-Binding FactorsHomeodomain ProteinsPc protein, Drosophilaphol protein, Drosophilapho protein, DrosophilaPhosphoproteinsPolycomb-Group ProteinsPolycomb Repressive Complex 1Repressor ProteinsTranscription FactorsYY1 Transcription Factor

Identifiers

PMID12628927
PMCPMC151054
OpenAlexW2086350426

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.