Evidence map›Paper›PMID 19035347›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2008

Cooperative interaction of Nkx2.5 and Mef2c transcription factors during heart development.

Joshua W Vincentz, Ralston M Barnes, Beth A Firulli, Simon J Conway, Anthony B Firulli

Open access · greenAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 105 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. The molecular mechanisms of cardiac development and related diseases.Signal transduction and targeted therapy · 2024
    Review
  9. Article
  10. Review
  11. Cardiac Transcription Factors and Regulatory Networks.Advances in experimental medicine and biology · 2024
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Comprehensive bioinformatics analysis forTranslational cancer research · 2022
    Article
  18. Review
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Joshua W VincentzRiley Heart Research Center, Herman B Wells Center for Pediatric Research Division of Pediatrics Cardiology, Department of Anatomy, Indiana Medical School, Indianapolis, Indiana 46202-5225, USA.
Ralston M Barnes
Beth A Firulli
Simon J Conway
Anthony B Firulli
Indiana University – Purdue University Indianapolis · US

Funding

REGULATION OF CARDIOMYOCYTE SURVIVALP01HL085098 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FIELD, LOREN J · 2007 to 2011
$10.9M
TRANSCRIPTION FACTORS INVOLVED IN HEART DEVELOPMENTR01HL061677 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI FIRULLI, ANTHONY B. · 1999 to 2010
$3.5M
Cancer Biology Training ProgramT32CA111198 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI ROMAN, ANN · 2005 to 2009
$1.8M
NCI NIH HHS T32 CA111198NCI NIH HHS T32CA111198NHLBI NIH HHS 1P01HL085098-01A1NHLBI NIH HHS P01 HL085098NHLBI NIH HHS R01 HL061677NHLBI NIH HHS R01HL061677-09
6 · The paper itself

Abstract

The interactions of diverse transcription factors mediate the molecular programs that regulate mammalian heart development. Among these, Nkx2.5 and the Mef2c regulate common downstream targets and exhibit striking phenotypic similarities when disrupted, suggesting a potential interaction during heart development. Co-immunoprecipitation and mammalian two-hybrid experiments revealed a direct molecular interaction between Nkx2.5 and Mef2c. Assessment of mRNA expression verified spatiotemporal cardiac coexpression. Finally, genetic interaction studies employing histological and molecular analyses showed that, although Nkx2.5(-/-) and Mef2c(-/-) individual mutants both have identifiable ventricles, Nkx2.5(-/-);Mef2c(-/-) double mutants do not, and that mutant cardiomyocytes express only atrial and second heart field markers. Molecular marker and cell death and proliferation analyses provide evidence that ventricular hypoplasia is the result of defective ventricular cell differentiation. Collectively, these data support a hypothesis where physical, functional, and genetic interactions between Nkx2.5 and Mef2c are necessary for ventricle formation.

Indexed as

AnimalsCell DifferentiationCell LineGene Expression Regulation, DevelopmentalHeartHomeobox Protein Nkx-2.5Homeodomain ProteinsHumansMEF2 Transcription FactorsMiceMice, KnockoutMutationMyocardiumMyogenic Regulatory FactorsProtein BindingTranscription FactorsHomeobox Protein Nkx-2.5Homeodomain ProteinsMef2c protein, mouseMEF2 Transcription FactorsMyogenic Regulatory FactorsNkx2-5 protein, mouseTranscription Factors

Identifiers

PMID19035347
PMCPMC2639719
OpenAlexW2095158850

What OpenQuestion holds

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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.