PUBLICATION
Multiplicity of neruopeptide Y receptors: cloning of a third distinct subtype in the zebrafish
- Authors
- Ringvall, M., Berglund, M.M., and Larhammar, D.
- ID
- ZDB-PUB-980123-1
- Date
- 1997
- Source
- Biochemical and Biophysical Research Communications 241: 749-755 (Journal)
- Registered Authors
- Larhammar, Dan
- Keywords
- none
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- CHO Cells
- Cloning, Molecular
- Colforsin/pharmacology
- Cricetinae
- Cyclic AMP/antagonists & inhibitors
- Cyclic AMP/biosynthesis
- Humans
- Mice
- Molecular Sequence Data
- Protein Binding/genetics
- Receptors, Neuropeptide Y/genetics*
- Receptors, Neuropeptide Y/isolation & purification*
- Receptors, Neuropeptide Y/physiology
- Swine
- Zebrafish/genetics*
- PubMed
- 9434780 Full text @ Biochem. Biophys. Res. Commun.
Citation
Ringvall, M., Berglund, M.M., and Larhammar, D. (1997) Multiplicity of neruopeptide Y receptors: cloning of a third distinct subtype in the zebrafish. Biochemical and Biophysical Research Communications. 241:749-755.
Abstract
Five different receptor subtypes for neuropeptide Y (NPY) have recently been cloned in mammals. We have discovered three distinct subtypes by PCR in the zebrafish, Danio rerio, and describe here one of these called zYc. The protein sequence identity is 46-51% to mammalian subtypes Y1, Y4 and Y6 and to zebrafish Ya, i.e., the same degree of identity as these subtypes display to one another. The identity to zYb is higher, 75%, indicating that zYb and zYc share a more recent ancestor. The zYc receptor binds NPY and PYY (peptide YY) from mammals as well as zebrafish with high affinities and has a Kd of 16 pM for 125I-pPYY. The pharmacological profile is similar to, but distinct-from, mammalian Y1. zYc inhibits cAMP synthesis. This work suggests that NPY has more receptor subtypes than any other peptide that binds to G protein-coupled receptors. Work is in progress to see if the zebrafish receptors are present in mammals.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping