Evidence map›Paper›PMID 16024804›Full record

ArticleMolecular and cellular biology2005

Mammalian polyhomeotic homologues Phc2 and Phc1 act in synergy to mediate polycomb repression of Hox genes.

Kyo-Ichi Isono, Yu-Ichi Fujimura, Jun Shinga, Makoto Yamaki, Jiyang O-Wang, Yoshihiro Takihara, Yasuaki Murahashi, Yuki Takada, Yoko Mizutani-Koseki, Haruhiko Koseki

Erratum issuedAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

70 citing papers in PubMed, 140 citations in OpenAlex.

  1. Review
  2. Article
  3. Polycomb-mediated 3D chromatin interactions in gene regulation.Current opinion in genetics & development · 2026
    Review
  4. Article
  5. Review
  6. Polycomb function in early mouse development.Cell death and differentiation · 2025
    Review
  7. Indirect neurogenesis in space and time.Nature reviews. Neuroscience · 2024
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Kyo-Ichi IsonoRIKEN Research Center for Allergy and Immunology, 1-7-22 Suehiro, Tsurumi-ku, Yokohama 230-0045, Japan.
Yu-Ichi Fujimura
Jun Shinga
Makoto Yamaki
Jiyang O-Wang
Yoshihiro Takihara
Yasuaki Murahashi
Yuki Takada
Yoko Mizutani-Koseki
Haruhiko Koseki
RIKEN Center for Integrative Medical Sciences · JPChiba University · JPHiroshima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Polycomb group (PcG) gene products form multimeric protein complexes and contribute to anterior-posterior (A-P) specification via the transcriptional regulation of Hox cluster genes. The Drosophila polyhomeotic genes and their mammalian orthologues, Phc1, Phc2, and Phc3, encode nuclear proteins that are constituents of evolutionarily conserved protein complexes designated class II PcG complexes. In this study, we describe the generation and phenotypes of Phc2-deficient mice. We show posterior transformations of the axial skeleton and premature senescence of mouse embryonic fibroblasts associated with derepression of Hox cluster genes and Cdkn2a genes, respectively. Synergistic actions of a Phc2 mutation with Phc1 and Rnf110 mutations during A-P specification, coimmunoprecipitation of their products from embryonic extracts, and chromatin immunoprecipitation by anti-Phc2 monoclonal antibodies suggest that Hox repression by Phc2 is mediated through the class II PcG complexes, probably via direct binding to the Hox locus. The genetic interactions further reveal the functional overlap between Phc2 and Phc1 and a strict dose-dependent requirement during A-P specification and embryonic survival. Functional redundancy between Phc2 and Phc1 leads us to hypothesize that the overall level of polyhomeotic orthologues in nuclei is a parameter that is critical in enabling the class II PcG complexes to exert their molecular functions.

Indexed as

Genes, HomeoboxAnimalsBody PatterningCarrier ProteinsDNA-Binding ProteinsEmbryonic DevelopmentGene Expression Regulation, DevelopmentalHomeodomain ProteinsMiceOrgan SpecificityPolycomb-Group ProteinsPolycomb Repressive Complex 1Polycomb Repressive Complex 2Repressor ProteinsTranscription FactorsCarrier ProteinsDNA-Binding ProteinsHomeodomain ProteinsHoxb8 protein, mousePcgf6 protein, mousePhc1 protein, mousePhc2 protein, mousePolycomb-Group ProteinsPolycomb Repressive Complex 1Polycomb Repressive Complex 2Repressor ProteinsTranscription Factors

Identifiers

PMID16024804
PMCPMC1190356
OpenAlexW2122910069

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.