PUBLICATION
Fgf8a mutation affects craniofacial development and skeletal gene expression in zebrafish larvae
- Authors
- Gebuijs, I.G.E., Raterman, S.T., Metz, J.R., Swanenberg, L., Zethof, J., Van den Bos, R., Carels, C.E.L., Wagener, F.A.D.T.G., Von den Hoff, J.W.
- ID
- ZDB-PUB-190902-20
- Date
- 2019
- Source
- Biology Open 8(9): (Journal)
- Registered Authors
- Metz, Juriaan R.
- Keywords
- Bone, Cartilage, Craniofacial development, FGF8, Gene expression, Morphology, Zebrafish
- MeSH Terms
- none
- PubMed
- 31471293 Full text @ Biol. Open
Citation
Gebuijs, I.G.E., Raterman, S.T., Metz, J.R., Swanenberg, L., Zethof, J., Van den Bos, R., Carels, C.E.L., Wagener, F.A.D.T.G., Von den Hoff, J.W. (2019) Fgf8a mutation affects craniofacial development and skeletal gene expression in zebrafish larvae. Biology Open. 8(9):.
Abstract
Craniofacial development is tightly regulated and therefore highly vulnerable to disturbance by genetic and environmental factors. Fibroblast growth factors (FGFs) direct migration, proliferation and survival of cranial neural crest cells (CNCCs) forming the human face. In this study, we analyzed bone and cartilage formation in the head of 5 dpf fgf8ati282 zebrafish larvae and assessed gene expression levels for 11 genes involved in these processes. In addition, in situ hybridization was performed on 8 and 24 hpf larvae (fgf8a, dlx2a, runx2a, col2a1a). A significant size reduction of 8 out of 9 craniofacial cartilage structures was found in homozygous mutant (6-36%, p<0.01) and heterozygous (7-24%, p<0.01) larvae. Also, 9 mineralized structures were not observed in all or part of the homozygous (0-71%, p<0.0001) and heterozygous (33-100%, p<0.0001) larvae. In homozygote mutants, runx2a and sp7 expression was upregulated compared to wildtypes, presumably to compensate for the reduced bone formation. Decreased col9a1b expression may compromise cartilage formation. Upregulated dlx2a in homozygotes indicates impaired CNCC function. Dlx2a expression was reduced in the first and second stream of CNCCs in homozygous mutants at 24 hpf, as shown by in situ hybridization. This indicates an impairment of CNCC migration and survival.by fgf8 mutation.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping