PUBLICATION
Expression of trpC1 and trpC6 orthologs in zebrafish
- Authors
- Möller, C.C., Mangos, S., Drummond, I.A., and Reiser, J.
- ID
- ZDB-PUB-080408-13
- Date
- 2008
- Source
- Gene expression patterns : GEP 8(5): 291-296 (Journal)
- Registered Authors
- Drummond, Iain, Mangos, Steve
- Keywords
- Transient receptor potential; ion channel; smooth muscle; in situ hybridization
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Calcium Channels/genetics*
- Cloning, Molecular
- Conserved Sequence
- DNA, Complementary
- Embryo, Nonmammalian
- In Situ Hybridization
- Molecular Sequence Data
- Muscle, Smooth/metabolism
- Phylogeny
- Protein Structure, Tertiary
- Sequence Homology, Amino Acid
- TRPC Cation Channels/chemistry
- TRPC Cation Channels/genetics
- TRPC Cation Channels/metabolism*
- Zebrafish/embryology
- Zebrafish/genetics
- Zebrafish/metabolism*
- Zebrafish Proteins/chemistry
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- PubMed
- 18378501 Full text @ Gene Expr. Patterns
Citation
Möller, C.C., Mangos, S., Drummond, I.A., and Reiser, J. (2008) Expression of trpC1 and trpC6 orthologs in zebrafish. Gene expression patterns : GEP. 8(5):291-296.
Abstract
Transient receptor potential (TRP) genes encode subunits that form cation-selective ion channels in a variety of organisms and cell types. TRP channels serve diverse functions ranging from thermal, tactile, taste, and osmolar sensing to fluid flow sensing. TRPC1 and TRPC6 belong to the TRPC subfamily, members of which are thought to contribute to several cellular events such as regulated migration of neuronal dendrites, contractile responses of smooth muscle cells and maintenance of the structural integrity of kidney podocytes. Pathogenic roles have been suggested for TRPC1 in asthma and chronic obstructive pulmonary disease, and TRPC6 dysfunction was recently linked to proteinuric kidney disease. To explore the potential roles for TRPC channels in zebrafish organ function, we cloned zebrafish trpC1 and trpC6 cDNAs, and investigated their expression during zebrafish development. We detected trpC1 expression in the head, in cells surrounding the outflow tract of the heart, and in the ganglion cells as well as the inner nuclear layer of the eye. trpC6 expression was detected in the head, pectoral fins, aortic endothelial cells, and gastrointestinal smooth muscle cells. Our results point to roles of TRPC channels in several tissues during zebrafish development, and suggest that the zebrafish may be a suitable model system to study the pathophysiology of TRPC1 and TRPC6 in specific cell types.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping