PUBLICATION
Zebrafish tenascin-W, a new member of the tenascin family
- Authors
- Weber, P., Montag, D., Schachner, M., and Bernhardt, R.R.
- ID
- ZDB-PUB-980421-5
- Date
- 1998
- Source
- Journal of neurobiology 35: 1-16 (Journal)
- Registered Authors
- Bernhardt, Robert, Schachner, Melitta
- Keywords
- extracellular matrix; zebrafish; epidermal growth factor-like repeats; fibronectin type III-like repeats; neural crest
- MeSH Terms
-
- Aging/metabolism
- Amino Acid Sequence
- Animals
- Blotting, Northern
- Cloning, Molecular
- DNA, Complementary/genetics
- DNA, Complementary/isolation & purification
- Larva/metabolism
- Molecular Sequence Data
- Protein Conformation
- RNA, Messenger/metabolism
- Tenascin/genetics*
- Tissue Distribution
- Zebrafish/embryology
- Zebrafish/growth & development
- Zebrafish/metabolism*
- Zebrafish Proteins*
- PubMed
- 9552162 Full text @ J. Neurobiol.
Citation
Weber, P., Montag, D., Schachner, M., and Bernhardt, R.R. (1998) Zebrafish tenascin-W, a new member of the tenascin family. Journal of neurobiology. 35:1-16.
Abstract
A cDNA clone encoding tenascin-W, a novel member of the tenascin family, was isolated from a 20- to 28-h postfertilization (hpf) zebrafish cDNA library on the basis of the conserved epidermal growth factor-like domains represented in all tenascin molecules. An open reading frame of 2796 base pairs encodes a mature protein consisting of heptad repeats, a cysteine-rich amino terminal region, 3.5 epidermal growth factor-like repeats, five fibronectin type III homologous repeats, and a domain homologous to fibrinogen. These domains are the typical modular elements of molecules of the tenascin family. Sequence comparison demonstrated that TN-W shares homologies with the members of the tenascin family but is not a species homolog of any identified tenascin. The expression pattern of tn-w was analyzed by in situ hybridization in 1-day-old embryos, in 3-day-old larvae, and in juvenile zebrafish. At 24-25 hpf, tn-w mRNA was expressed in the lateral plate mesoderm, most conspicuously in the presumptive sclerotome. Migrating cells of sclerotomal and neural crest origins also showed high levels of expression. At 3 days, expression by sclerotomal and neural crest cells continued to be observed while expression in the somitic mesoderm was decreased. In juvenile fish, tn-w was expressed weakly by cells in the myosepta and, more strongly, by presumably nonneuronal cells in the dorsal root ganglia. In these tissues and at the same developmental stages, the expression of tn-w partially overlapped with the distribution of tn-c mRNA. In addition, tn-c was expressed in the central nervous system (CNS) and in the axial mesoderm, neither of which expressed tn-w at any of the age stages examined. The expression pattern of tn-w suggests an involvement in neural crest and sclerotome cell migration and in the formation of the skeleton. Similar and possibly overlapping functions could also be performed by tn-c, which appears to have additional functions during the development of the CNS.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping