PUBLICATION
Zebrafish fgfr1 is a member of the fgf8 synexpression group and is required for fgf8 signalling at the midbrain-hindbrain boundary
- Authors
- Scholpp, S., Groth, C., Lohs, C., Lardelli, M., and Brand, M.
- ID
- ZDB-PUB-040526-3
- Date
- 2004
- Source
- Development genes and evolution 214(6): 285-295 (Journal)
- Registered Authors
- Brand, Michael, Groth, Casper, Lardelli, Michael, Lohs, Claudia, Scholpp, Steffen
- Keywords
- Fibroblast growth factor receptor 1, Fgf8, Midbrain-hindbrain boundary, Zebrafish, Acerebellar
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Cloning, Molecular
- Evolution, Molecular
- Fibroblast Growth Factor 8
- Fibroblast Growth Factors/genetics
- Fibroblast Growth Factors/metabolism*
- Mesencephalon/embryology
- Mesencephalon/metabolism
- Molecular Sequence Data
- Phenotype
- Phylogeny
- Receptor Protein-Tyrosine Kinases/genetics*
- Receptor Protein-Tyrosine Kinases/metabolism
- Receptor, Fibroblast Growth Factor, Type 1
- Receptors, Fibroblast Growth Factor/genetics*
- Receptors, Fibroblast Growth Factor/metabolism
- Rhombencephalon/embryology
- Rhombencephalon/metabolism
- Sequence Homology, Amino Acid
- Signal Transduction
- Zebrafish/embryology
- Zebrafish/genetics*
- Zebrafish/metabolism
- PubMed
- 15221377 Full text @ Dev. Genes Evol.
Citation
Scholpp, S., Groth, C., Lohs, C., Lardelli, M., and Brand, M. (2004) Zebrafish fgfr1 is a member of the fgf8 synexpression group and is required for fgf8 signalling at the midbrain-hindbrain boundary. Development genes and evolution. 214(6):285-295.
Abstract
FGFR1 is an important signalling molecule during embryogenesis and in adulthood. FGFR1 mutations in human may lead to developmental defects and pathological conditions, including cancer and Alzheimer's disease. Here, we describe cloning and expression analysis of the zebrafish fibroblast growth factor receptor 1 ( fgfr1). Initially, fgfr1 is expressed in the adaxial mesoderm with transcripts distinctly localised to the anterior portion of each half-somite. Hereupon, fgfr1 is also strongly expressed in the otic vesicles, branchial arches and the brain, especially at the midbrain-hindbrain boundary (MHB). The expression patterns of fgfr1 and fgf8 are strikingly similar and knock-down of fgfr1 phenocopies many aspects observed in the fgf8 mutant acerebellar, suggesting that Fgf8 exerts its function mainly by binding to FgfR1.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping