PUBLICATION
Chamber identity programs drive early functional partitioning of the heart
- Authors
- Mosimann, C., Panáková, D., Werdich, A.A., Musso, G., Burger, A., Lawson, K.L., Carr, L.A., Nevis, K.R., Sabeh, M.K., Zhou, Y., Davidson, A.J., DiBiase, A., Burns, C.E., Burns, C.G., MacRae, C.A., Zon, L.I.
- ID
- ZDB-PUB-150827-4
- Date
- 2015
- Source
- Nature communications 6: 8146 (Journal)
- Registered Authors
- Burger, Alexa, Burns (Erter), Caroline, Davidson, Alan, DiBiase, Anthony, MacRae, Calum A., Mosimann, Christian, Panáková, Daniela, Zhou, Yi, Zon, Leonard I.
- Keywords
- none
- Datasets
- GEO:GSE70881, GEO:GSE70750
- MeSH Terms
-
- Regulatory Elements, Transcriptional/genetics
- Salivary Proteins and Peptides/genetics
- Salivary Proteins and Peptides/metabolism
- Embryo, Nonmammalian
- Latent TGF-beta Binding Proteins/genetics
- Latent TGF-beta Binding Proteins/metabolism
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism
- Animals, Genetically Modified
- LIM Domain Proteins/genetics
- LIM Domain Proteins/metabolism
- Heart Atria/embryology*
- Heart Atria/metabolism
- Transcription Factors/genetics
- Transcription Factors/metabolism
- Myocardium/metabolism*
- Zebrafish
- Cadherins/genetics
- Cadherins/metabolism
- Animals
- Heart/embryology
- Gene Expression Regulation, Developmental
- Heart Ventricles/embryology*
- Heart Ventricles/metabolism
- T-Box Domain Proteins/genetics
- T-Box Domain Proteins/metabolism
- Myosin Light Chains/genetics
- Myosin Light Chains/metabolism
- Myocytes, Cardiac/metabolism*
- Mesoderm/embryology
- Mesoderm/metabolism
- PubMed
- 26306682 Full text @ Nat. Commun.
Citation
Mosimann, C., Panáková, D., Werdich, A.A., Musso, G., Burger, A., Lawson, K.L., Carr, L.A., Nevis, K.R., Sabeh, M.K., Zhou, Y., Davidson, A.J., DiBiase, A., Burns, C.E., Burns, C.G., MacRae, C.A., Zon, L.I. (2015) Chamber identity programs drive early functional partitioning of the heart. Nature communications. 6:8146.
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.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping