Abstract
Three gonadotropin-releasing hormones (GnRHs) and three cognate receptors have been identified in vertebrates, with distinct distributions and functions. According to their sequences, the receptors can be grouped into distinct classes: types I, II, and III. One branch contains all type-I GnRH receptors (GnRH-R-I) from mammals and fish; another branch clusters mainly amphibian and human type-II GnRH receptors; and a third branch includes evolved fish, mainly perciform species, type-III GnRH receptors. Taken tilapia GnRH receptors as a model, the present study summarizes the information regarding the amino-acid residues assumed to be involved in the receptors' structure, binding, activation, and intracellular signal transduction, including arrangement of the disulfide bonds, glycosylation sites, coupling to G proteins, and protein kinase A or protein kinase C phosphorylation sites.
Original language | English |
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Pages (from-to) | 67-73 |
Number of pages | 7 |
Journal | General and Comparative Endocrinology |
Volume | 142 |
Issue number | 1-2 SPEC. ISS. |
DOIs | |
State | Published - 15 May 2005 |
Bibliographical note
Funding Information:This work was supported by Grant 775/01 from the Israel Science Foundation.
Keywords
- Disulfide bond
- G protein
- GPCR
- Glycosylation
- GnRH
- PKA
- PKC
- Phosphorylation
- Receptor
- Tilapia