Evidence map›Paper›PMID 26306682›Full record

ArticleNature communications2015

Chamber identity programs drive early functional partitioning of the heart.

Christian Mosimann, Daniela Panáková, Andreas A Werdich, Gabriel Musso, Alexa Burger, Katy L Lawson, Logan A Carr, Kathleen R Nevis, M Khaled Sabeh, Yi Zhou and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

67 citing papers in PubMed, 127 citations in OpenAlex.

  1. Role of CHD chromatin remodelers in heart development.World journal of pediatrics : WJP · 2026
    Review
  2. Coordination of cardiogenesis in vivo and in vitro.Nature reviews. Molecular cell biology · 2026
    Review
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  11. Science advances · 2024
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  14. bioRxiv : the preprint server for biology · 2023
    Article
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7 more citing papers are in PubMed but not listed here.

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

16 authors at 7 institutions in 2 countries.

Christian MosimannHoward Hughes Medical Institute, Boston, Massachusetts 02115, USA.
Daniela PanákováCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Andreas A WerdichCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Gabriel MussoCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Alexa BurgerInstitute of Molecular Life Sciences (IMLS), University of Zürich, 8057 Zürich, Switzerland.
Katy L LawsonHoward Hughes Medical Institute, Boston, Massachusetts 02115, USA.
Logan A CarrHoward Hughes Medical Institute, Boston, Massachusetts 02115, USA.
Kathleen R NevisCardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts 02129, USA.
M Khaled SabehCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Yi ZhouHoward Hughes Medical Institute, Boston, Massachusetts 02115, USA.
Alan J DavidsonHoward Hughes Medical Institute, Boston, Massachusetts 02115, USA.
Anthony DiBiaseHoward Hughes Medical Institute, Boston, Massachusetts 02115, USA.
Caroline E BurnsCardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts 02129, USA.
C Geoffrey BurnsCardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts 02129, USA.
Calum A MacRaeCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Leonard I ZonHoward Hughes Medical Institute, Boston, Massachusetts 02115, USA.
Brigham and Women's Hospital · USHoward Hughes Medical Institute · USBoston Children's Hospital · USHarvard University · USMassachusetts General Hospital · USUniversity of Zurich · CHHarvard Stem Cell Institute · US

Funding

MULTIDISCIPLINARY RESEARCH TRAINING IN CARDIOLOGYT32HL007208 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Patrick Thomas Ellinor, David E Sosnovik · 1985 to 2026
$16.1M
A Community Zebrafish Resource for Modeling GWAS BiologyR24OD017870 · OD · BRIGHAM AND WOMEN'S HOSPITAL · PI GOESSLING, WOLFRAM, MACRAE, CALUM A. · 2014 to 2021
$6.3M
EMBRYONIC HEMATOPOIESISR01HL048801 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI ZON, LEONARD IRA · 1992 to 2016
$5.7M
Genetic Determinants of Outflow Tract MorphogenesisR01HL096816 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BURNS, C. GEOFFREY · 2010 to 2014
$2.2M
Molecular Mechanisms of Stretch-Induced Electrical Remodeling in the HeartR00HL112724 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI WERDICH, ANDREAS AUGUSTINUS · 2015 to 2018
$747k
Howard Hughes Medical InstituteNHLBI NIH HHS 5R01HL048801-19NHLBI NIH HHS R00 HL112724NHLBI NIH HHS R01 HL048801NHLBI NIH HHS R01 HL096816NHLBI NIH HHS T32 HL007208NIH HHS R24 OD017870
6 · The paper itself

Abstract

The vertebrate heart muscle (myocardium) develops from the first heart field (FHF) and expands by adding second heart field (SHF) cells. While both lineages exist already in teleosts, the primordial contributions of FHF and SHF to heart structure and function remain incompletely understood. Here we delineate the functional contribution of the FHF and SHF to the zebrafish heart using the cis-regulatory elements of the draculin (drl) gene. The drl reporters initially delineate the lateral plate mesoderm, including heart progenitors. Subsequent myocardial drl reporter expression restricts to FHF descendants. We harnessed this unique feature to uncover that loss of tbx5a and pitx2 affect relative FHF versus SHF contributions to the heart. High-resolution physiology reveals distinctive electrical properties of each heart field territory that define a functional boundary within the single zebrafish ventricle. Our data establish that the transcriptional program driving cardiac septation regulates physiologic ventricle partitioning, which successively provides mechanical advantages of sequential contraction.

Indexed as

AnimalsAnimals, Genetically ModifiedCadherinsEmbryo, NonmammalianGene Expression Regulation, DevelopmentalHeartHeart AtriaHeart VentriclesLatent TGF-beta Binding ProteinsLIM Domain ProteinsMesodermMyocardiumMyocytes, CardiacMyosin Light ChainsRegulatory Elements, TranscriptionalSalivary Proteins and PeptidesCadherinsCDH17 protein, zebrafishdraculinLatent TGF-beta Binding ProteinsLIM Domain Proteinslmo2 protein, zebrafishLtbp3 protein, zebrafishMyosin Light ChainsPitx2 protein, zebrafishSalivary Proteins and PeptidesT-Box Domain ProteinsT-box transcription factor 5Transcription FactorsZebrafish Proteins

Identifiers

PMID26306682
PMCPMC4560818
OpenAlexW1846384077

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.