PUBLICATION
Expression of two isoforms of the vacuolar-type ATPase subunit B in the zebrafish Danio rerio
- Authors
- Boesch, S.T., Eller, B., and Pelster, B.
- ID
- ZDB-PUB-030602-3
- Date
- 2003
- Source
- The Journal of experimental biology 206(11): 1907-1915 (Journal)
- Registered Authors
- Pelster, Bernd
- Keywords
- none
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Blotting, Western
- DNA Primers
- Gene Expression Profiling*
- Immunohistochemistry
- Isoenzymes/genetics
- Isoenzymes/metabolism
- Molecular Sequence Data
- Sequence Alignment
- Vacuolar Proton-Translocating ATPases/genetics*
- Vacuolar Proton-Translocating ATPases/metabolism*
- Zebrafish/genetics*
- Zebrafish/metabolism*
- PubMed
- 12728012 Full text @ J. Exp. Biol.
Citation
Boesch, S.T., Eller, B., and Pelster, B. (2003) Expression of two isoforms of the vacuolar-type ATPase subunit B in the zebrafish Danio rerio. The Journal of experimental biology. 206(11):1907-1915.
Abstract
In the present study we tested the hypothesis that two isoforms of the regulatory subunit B of vacuolar-type ATPase (V-ATPase) are expressed in the zebrafish Danio rerio. The complete coding sequences for both isoforms, vatB1 and vatB2, were cloned and sequenced. BLASTX analysis revealed the greatest similarity to amino acid sequences of B subunits from the European eel Anguilla anguilla and rainbow trout Oncorhynchus mykiss. The isoforms were expressed in a bacterial system and the recombinant proteins verified using isoform-specific antibodies directed against vatB isoforms of the eel. The distribution of both isoforms in zebrafish tissues was investigated using reverse transcriptase-polymerase chain reaction and western blot analysis. The results revealed that at the RNA level both isoforms were expressed in all tested organs, i.e. the gills, swimbladder, heart, kidney, liver, spleen, intestine and skeletal muscle. At the protein level, however, there were tissue-specific variations in the levels of the two vatB isoforms expressed. The highest amounts of V-ATPase were detected in total protein preparations from gill, heart and liver tissue. In liver tissue, however, the western blot analysis indicated that vatB1 was not as prominent as vatB2, and immunohistochemistry revealed that antibodies directed against vatB1 yielded a very weak staining in a number of cells, while an antibody directed against vatB1 and vatB2 yielded a strong staining in virtually every cell. Similarly, neurosecretory cells of the small intestine were stained with an antibody directed against vatB1 and vatB2, but not with an antibody specific for vatB1. Therefore we conclude that the differential expression of two isoforms of the V-ATPase subunits, which may serve different functions as in several mammalian species, may also be a common phenomenon in teleost fish.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping