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Molecular evolution of multiple forms of kisspeptins and GPR54 receptors in vertebrates

Authors :
Hyuk Bang Kwon
Jong Ik Hwang
Tomohiro Osugi
Kyungjin Kim
Yuya Sunakawa
Naohito Otaki
Hubert Vaudry
Jae Young Seong
Yeo Reum Lee
K Tsunekawa
Mi Jin Moon
Haet Nim Um
Kazuyoshi Tsutsui
Source :
Endocrinology. 150(6)
Publication Year :
2009

Abstract

Kisspeptin and its receptor GPR54 play important roles in mammalian reproduction and cancer metastasis. Because the KiSS and GPR54 genes have been identified in a limited number of vertebrate species, mainly in mammals, the evolutionary history of these genes is poorly understood. In the present study, we have cloned multiple forms of kisspeptin and GPR54 cDNAs from a variety of vertebrate species. We found that fish have two forms of kisspeptin genes, KiSS-1 and KiSS-2, whereas Xenopus possesses three forms of kisspeptin genes, KiSS-1a, KiSS-1b, and KiSS-2. The nonmammalian KiSS-1 gene was found to be the ortholog of the mammalian KiSS-1 gene, whereas the KiSS-2 gene is a novel form, encoding a C-terminally amidated dodecapeptide in the Xenopus brain. This study is the first to identify a mature form of KiSS-2 product in the brain of any vertebrate. Likewise, fish possess two receptors, GPR54-1 and GPR54-2, whereas Xenopus carry three receptors, GPR54-1a, GPR54-1b, and GPR54-2. Sequence identity and genome synteny analyses indicate that Xenopus GPR54-1a is a human GPR54 ortholog, whereas Xenopus GPR54-1b is a fish GPR54-1 ortholog. Both kisspeptins and GPR54s were abundantly expressed in the Xenopus brain, notably in the hypothalamus, suggesting that these ligand-receptor pairs have neuroendocrine and neuromodulatory roles. Synthetic KiSS-1 and KiSS-2 peptides activated GPR54s expressed in CV-1 cells with different potencies, indicating differential ligand selectivity. These data shed new light on the molecular evolution of the kisspeptin-GPR54 system in vertebrates.

Details

ISSN :
19457170
Volume :
150
Issue :
6
Database :
OpenAIRE
Journal :
Endocrinology
Accession number :
edsair.doi.dedup.....e893b1b5d87a37636e12d19f0851959e