Evidence map›Paper›PMID 23850773›Full record

ArticleDevelopmental biology2013

Small heat shock proteins Hspb7 and Hspb12 regulate early steps of cardiac morphogenesis.

Gabriel E Rosenfeld, Emily J Mercer, Christopher E Mason, Todd Evans

Open access · hybridAbstract read
In one paragraph

Article in Developmental biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. A Combined HumanFrontiers in pharmacology · 2022
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Chaperones and Beyond as Key Players in Pluripotency Maintenance.Frontiers in cell and developmental biology · 2019
    Review
  9. Article
  10. Article
  11. Genetics of Cardiovascular Disease: Fishing for Causality.Frontiers in cardiovascular medicine · 2018
    Review
  12. HSPB7 is indispensable for heart development by modulating actin filament assembly.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Kupffer's vesicle size threshold for robust left-right patterning of the zebrafish embryo.Developmental dynamics : an official publication of the American Association of Anatomists · 2016
    Article
  18. Article
  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

4 authors at 1 institution in 1 country.

Gabriel E RosenfeldDepartment of Surgery, Weill Cornell Medical College, NY 10065, USA.
Emily J Mercer
Christopher E Mason
Todd Evans
Cornell University · US

Funding

Training Program in Developmental BiologyT32HD060600 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI BAO, ZHIRONG, STUHLMANN, HEIDI · 2010 to 2024
$3.5M
A molecular pathway controlling cardiomyocyte specification.R01HL111400 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI EVANS, TODD R · 2012 to 2016
$2.1M
NHLBI NIH HHS R01 HL111400NHLBI NIH HHS R01HL111400NICHD NIH HHS T32 HD060600NICHD NIH HHS T32HD060600
6 · The paper itself

Abstract

Cardiac morphogenesis is a complex multi-stage process, and the molecular basis for controlling distinct steps remains poorly understood. Because gata4 encodes a key transcriptional regulator of morphogenesis, we profiled transcript changes in cardiomyocytes when Gata4 protein is depleted from developing zebrafish embryos. We discovered that gata4 regulates expression of two small heat shock genes, hspb7 and hspb12, both of which are expressed in the embryonic heart. We show that depletion of Hspb7 or Hspb12 disrupts normal cardiac morphogenesis, at least in part due to defects in ventricular size and shape. We confirmed that gata4 interacts genetically with the hspb7/12 pathway, but surprisingly, we found that hspb7 also has an earlier, gata4-independent function. Depletion perturbs Kupffer's vesicle (KV) morphology leading to a failure in establishing the left-right axis of asymmetry. Targeted depletion of Hspb7 in the yolk syncytial layer is sufficient to disrupt KV morphology and also causes an even earlier block to heart tube formation and a bifid phenotype. Recently, several genome-wide association studies found that HSPB7 SNPs are highly associated with idiopathic cardiomyopathies and heart failure. Therefore, GATA4 and HSPB7 may act alone or together to regulate morphogenesis with relevance to congenital and acquired human heart disease.

Indexed as

Gene Expression Regulation, DevelopmentalMorphogenesisAnimalsBody PatterningEmbryonic DevelopmentEmbryo, NonmammalianGATA Transcription FactorsHeart VentriclesHeat-Shock Proteins, SmallKupffer CellsMorpholinosMyocytes, CardiacOrgan SizePolymorphism, Single NucleotideTranscriptional ActivationZebrafishGata4 protein, zebrafishGATA Transcription FactorsHeat-Shock Proteins, SmallMorpholinosZebrafish ProteinsCardiogenesisGata4Heart developmentKupffer's vesicleYSLZebrafish

Identifiers

PMID23850773
PMCPMC3777613
OpenAlexW2014738859

What OpenQuestion holds

Textmetadata
LicenceTDM
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.