Evidence map›Paper›PMID 40605499›Full record

ArticleJournal of experimental zoology. Part B, Molecular and developmental evolution2025

The Interplay of Ontogeny and Phylogeny at the Transcriptome Level of the Tetrapod Heart.

G A Cordero, A K Holloway, T Friedrich, J Eme, W Eckalbar, K Kusumi, F J Janzen, J W Hicks, F L Conlon, B G Bruneau and 1 more

Abstract read
In one paragraph

Article in Journal of experimental zoology. Part B, Molecular and developmental evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

G A CorderoCavanilles Institute of Biodiversity and Evolutionary Biology, University of Valencia, Paterna, Valencia, Spain.ORCID https://orcid.org/0000-0002-9137-1741
A K HollowayGladstone Institutes, San Francisco, California, USA.
T FriedrichGladstone Institutes, San Francisco, California, USA.
J EmeDepartment of Biological Sciences, California State University San Marcos, San Marcos, California, USA.
W EckalbarSchool of Life Sciences, Arizona State University, Tempe, Arizona, USA.
K KusumiSchool of Life Sciences, Arizona State University, Tempe, Arizona, USA.
F J JanzenW.K. Kellogg Biological Station, Michigan State University, Hickory Corners, Michigan, USA.
J W HicksDepartment of Ecology and Evolutionary Biology, University of California Irvine, Irvine, California, USA.
F L ConlonDepartment of Biology and Genetics, McAllister Heart Institute, University of North Carolina Chapel Hill, Chapel Hill, North Carolina, USA.
B G BruneauGladstone Institutes, San Francisco, California, USA.
K S PollardGladstone Institutes, San Francisco, California, USA.

Funding

The Epigenetic Landscape of Heart DevelopmentUM1HL098179 · NHLBI · J. DAVID GLADSTONE INSTITUTES · PI BRUNEAU, BENOIT GAETAN, POLLARD, KATHERINE S. · 2015 to 2019
$4.7M
NHLBI NIH HHS UM1 HL098179This study was funded in part by the NHLBI Bench to Bassinet consortium (UM1HL098179 to B.G.B.).
6 · The paper itself

Abstract

The tetrapod heart is characterized by three chambers in amphibians and non-avian reptiles, as opposed to four in birds, crocodilians and mammals. We explored this diversity via the most phylogenetically comprehensive comparison of heart transcriptomes undertaken to date. Transcriptomes representing the ontogeny of heart compartmentalization (septation) in alligator, chicken, frog, mouse, lizard and turtle embryos exhibited a clear species-specific signal, which was driven by genes involved in heart contraction. During the stage dominated by septation-related tissue transformations, the most highly expressed genes shared by species originated before the tetrapods diversified and were related to septum morphogenesis, ventricular development, and chamber formation. The expression of septation-related genes did not adhere to phylogeny or heart chamber number, and genes differentially expressed across developmental stages within species varied in their evolutionary ages and predicted functions. We discuss how the acquisition of novel structures in some lineages, convergent evolution of four heart chambers, embryonic metabolism, microstructural variation, and ontogenetic shifts (heterochronies), collectively, provide insight into evolved and conserved patterns of transcriptome-level variation. These data serve as a resource to further stimulate evo-devo research on complex organ systems, such as the heart.

Indexed as

HeartPhylogenyReptilesTranscriptomeVertebratesAnimalsBiological EvolutionGene Expression Regulation, DevelopmentalMiceSpecies Specificitycomparative transcriptomicsevo‐devoheart developmenttetrapod embryology

Identifiers

PMID40605499
PMCPMC12328841

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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.