PUBLICATION
The zebrafish HGF receptor met controls migration of myogenic progenitor cells in appendicular development
- Authors
- Nord, H., Dennhag, N., Tydinger, H., von Hofsten, J.
- ID
- ZDB-PUB-190711-9
- Date
- 2019
- Source
- PLoS One 14: e0219259 (Journal)
- Registered Authors
- Nord, Hanna, von Hofsten, Jonas
- Keywords
- none
- MeSH Terms
-
- Animals
- CRISPR-Cas Systems
- Cell Movement/physiology
- Extremities/growth & development
- Gene Expression Regulation, Developmental/genetics
- Muscle Development/physiology
- Muscle Fibers, Skeletal/metabolism
- Muscle, Skeletal/metabolism
- Muscles/metabolism
- Proto-Oncogene Proteins c-met/genetics*
- Proto-Oncogene Proteins c-met/metabolism*
- Stem Cells/metabolism
- Zebrafish/embryology
- Zebrafish/genetics
- Zebrafish Proteins/metabolism
- PubMed
- 31287821 Full text @ PLoS One
Citation
Nord, H., Dennhag, N., Tydinger, H., von Hofsten, J. (2019) The zebrafish HGF receptor met controls migration of myogenic progenitor cells in appendicular development. PLoS One. 14:e0219259.
Abstract
The hepatocyte growth factor receptor C-met plays an important role in cellular migration, which is crucial for many developmental processes as well as for cancer cell metastasis. C-met has been linked to the development of mammalian appendicular muscle, which are derived from migrating muscle progenitor cells (MMPs) from within the somite. Mammalian limbs are homologous to the teleost pectoral and pelvic fins. In this study we used Crispr/Cas9 to mutate the zebrafish met gene and found that the MMP derived musculature of the paired appendages was severely affected. The mutation resulted in a reduced muscle fibre number, in particular in the pectoral abductor, and in a disturbed pectoral fin function. Other MMP derived muscles, such as the sternohyoid muscle and posterior hypaxial muscle were also affected in met mutants. This indicates that the role of met in MMP function and appendicular myogenesis is conserved within vertebrates.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping