Evidence map›Paper›PMID 24705708›Full record

ArticlePloS one2014

YY1 acts as a transcriptional activator of Hoxa5 gene expression in mouse organogenesis.

Félix-Antoine Bérubé-Simard, Christelle Prudhomme, Lucie Jeannotte

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Deletion ofDisease models & mechanisms · 2020
    Article
  5. Article
  6. Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  7. Article
  8. Hoxa5: A Key Player in Development and Disease.Journal of developmental biology · 2016
    Review
  9. Narrowing theClinical epigenetics · 2016
    Article
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

3 authors at 1 institution in 1 country.

Félix-Antoine Bérubé-SimardDepartment of Molecular Biology, Medical Biochemistry and Pathology, Université Laval, Québec, Canada; Centre de recherche sur le cancer de l'Université Laval, Québec, Canada; Centre de recherche du Centre Hospitalier Universitaire de Québec, L'Hôtel-Dieu de Québec, Québec, Canada.
Christelle PrudhommeDepartment of Molecular Biology, Medical Biochemistry and Pathology, Université Laval, Québec, Canada; Centre de recherche sur le cancer de l'Université Laval, Québec, Canada; Centre de recherche du Centre Hospitalier Universitaire de Québec, L'Hôtel-Dieu de Québec, Québec, Canada.
Lucie JeannotteDepartment of Molecular Biology, Medical Biochemistry and Pathology, Université Laval, Québec, Canada; Centre de recherche sur le cancer de l'Université Laval, Québec, Canada; Centre de recherche du Centre Hospitalier Universitaire de Québec, L'Hôtel-Dieu de Québec, Québec, Canada.
Hôtel-Dieu de Québec · CA

Funding

Canadian Institutes of Health Research MOP-15139
6 · The paper itself

Abstract

The Hox gene family encodes homeodomain-containing transcriptional regulators that confer positional information to axial and paraxial tissues in the developing embryo. The dynamic Hox gene expression pattern requires mechanisms that differentially control Hox transcription in a precise spatio-temporal fashion. This implies an integrated regulation of neighbouring Hox genes achieved through the sharing and the selective use of defined enhancer sequences. The Hoxa5 gene plays a crucial role in lung and gut organogenesis. To position Hoxa5 in the regulatory hierarchy that drives organ morphogenesis, we searched for cis-acting regulatory sequences and associated trans-acting factors required for Hoxa5 expression in the developing lung and gut. Using mouse transgenesis, we identified two DNA regions included in a 1.5-kb XbaI-XbaI fragment located in the Hoxa4-Hoxa5 intergenic domain and known to control Hoxa4 organ expression. The multifunctional YY1 transcription factor binds the two regulatory sequences in vitro and in vivo. Moreover, the mesenchymal deletion of the Yy1 gene function in mice results in a Hoxa5-like lung phenotype with decreased Hoxa5 and Hoxa4 gene expression. Thus, YY1 acts as a positive regulator of Hoxa5 expression in the developing lung and gut. Our data also support a role for YY1 in the coordinated expression of Hox genes for correct organogenesis.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBase SequenceBinding SitesGene OrderGene TargetingGenetic LociHomeodomain ProteinsLungMesodermMiceMice, TransgenicMolecular Sequence DataOrganogenesisOrgan SpecificityPhenotypeHomeodomain ProteinsHoxa5 protein, mousePhosphoproteinsTranscription FactorsYY1 Transcription Factor

Identifiers

PMID24705708
PMCPMC3976385
OpenAlexW2002024939

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.