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Molecular Evolution of Multiple Forms of Kisspeptins and GPR54 Receptors in Vertebrates

Authors
Lee, Yeo ReumTsunekawa, KentaMoon, Mi JinUm, Haet NimHwang, Jong-IkOsugi, TomohiroOtaki, NaohitoSunakawa, YuyaKim, KyungjinVaudry, HubertKwon, Hyuk BangSeong, Jae YoungTsutsui, Kazuyoshi
Issue Date
6월-2009
Publisher
ENDOCRINE SOC
Citation
ENDOCRINOLOGY, v.150, no.6, pp.2837 - 2846
Indexed
SCIE
SCOPUS
Journal Title
ENDOCRINOLOGY
Volume
150
Number
6
Start Page
2837
End Page
2846
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/119937
DOI
10.1210/en.2008-1679
ISSN
0013-7227
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. (Endocrinology 150: 2837-2846, 2009)
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