Evidence map›Paper›PMID 23775117›Full record

ArticleMolecular and cellular biology2013

Variable requirements for DNA-binding proteins at polycomb-dependent repressive regions in human HOX clusters.

Caroline J Woo, Peter V Kharchenko, Laurence Daheron, Peter J Park, Robert E Kingston

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Role of Hox genes in stem cell differentiation.World journal of stem cells · 2015
    Review
  14. Article
  15. Article
  16. Comprehensive comparative homeobox gene annotation in human and mouse.Database : the journal of biological databases and curation · 2015
    Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 3 institutions in 1 country.

Caroline J WooDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Peter V Kharchenko
Laurence Daheron
Peter J Park
Robert E Kingston
Harvard University · USCenter for Systems Biology · USMassachusetts General Hospital · US

Funding

Maintenance of Gene ExpressionR01GM043901 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI KINGSTON, ROBERT · 1991 to 2018
$10.7M
Integrative Analysis of Multiple Genomic Data SetsR01GM082798 · NIGMS · HARVARD MEDICAL SCHOOL · PI PARK, PETER J · 2007 to 2011
$1.5M
Long-range High-resolution Mapping of ChromatinR01HG003141 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI KINGSTON, ROBERT · 2003 to 2005
$1.3M
Long-range nucleosome mapping of the HOX gene clusterF32GM072265 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI WOO, CAROLINE · 2004 to 2006
$142k
NHGRI NIH HHS HG003141NHGRI NIH HHS R01 HG003141NIGMS NIH HHS F32 GM072265NIGMS NIH HHS GM072265NIGMS NIH HHS GM082798NIGMS NIH HHS GM43901NIGMS NIH HHS R01 GM043901NIGMS NIH HHS R01 GM082798
6 · The paper itself

Abstract

Polycomb group (PcG)-mediated repression is an evolutionarily conserved process critical for cell fate determination and maintenance of gene expression during embryonic development. However, the mechanisms underlying PcG recruitment in mammals remain unclear since few regulatory sites have been identified. We report two novel prospective PcG-dependent regulatory elements within the human HOXB and HOXC clusters and compare their repressive activities to a previously identified element in the HOXD cluster. These regions recruited the PcG proteins BMI1 and SUZ12 to a reporter construct in mesenchymal stem cells and conferred repression that was dependent upon PcG expression. Furthermore, we examined the potential of two DNA-binding proteins, JARID2 and YY1, to regulate PcG activity at these three elements. JARID2 has differential requirements, whereas YY1 appears to be required for repressive activity at all 3 sites. We conclude that distinct elements of the mammalian HOX clusters can recruit components of the PcG complexes and confer repression, similar to what has been seen in Drosophila. These elements, however, have diverse requirements for binding factors, which, combined with previous data on other loci, speaks to the complexity of PcG targeting in mammals.

Indexed as

Gene Expression Regulation, DevelopmentalMultigene FamilyAnimalsCells, CulturedDNA-Binding ProteinsGenes, HomeoboxHomeodomain ProteinsHumansMesenchymal Stem CellsPolycomb-Group ProteinsPolycomb Repressive Complex 2Regulatory Elements, TranscriptionalTranscription, GeneticDNA-Binding ProteinsHomeodomain ProteinsJARID2 protein, humanPolycomb-Group ProteinsPolycomb Repressive Complex 2

Identifiers

PMID23775117
PMCPMC3753906
OpenAlexW2134072110

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.