Multiple Kisspeptin Receptors in Early Osteichthyans Provide New Insights into the Evolution of This Receptor Family
Abstract
Deorphanization of GPR54 receptor a decade ago led to the characterization of the kisspeptin receptor (Kissr) in mammals
and the discovery of its major role in the brain control of reproduction. While a single gene encodes for Kissr in eutherian
mammals including human, other vertebrates present a variable number of Kissr genes, from none in birds, one or two in
teleosts, to three in an amphibian, xenopus. In order to get more insight into the evolution of Kissr gene family, we
investigated the presence of Kissr in osteichthyans of key-phylogenetical positions: the coelacanth, a representative of early
sarcopterygians, the spotted gar, a non-teleost actinopterygian, and the European eel, a member of an early group of
teleosts (elopomorphs). We report the occurrence of three Kissr for the first time in a teleost, the eel. As measured by
quantitative RT-PCR, the three eel Kissr were differentially expressed in the brain-pituitary-gonadal axis, and differentially
regulated in experimentally matured eels, as compared to prepubertal controls. Subfunctionalisation, as shown by these
differences in tissue distribution and regulation, may have represented significant evolutionary constraints for the
conservation of multiple Kissr paralogs in this species. Furthermore, we identified four Kissr in both coelacanth and spotted
gar genomes, providing the first evidence for the presence of four Kissr in vertebrates. Phylogenetic and syntenic analyses
supported the existence of four Kissr paralogs in osteichthyans and allowed to propose a clarified nomenclature of Kissr
(Kissr-1 to -4) based on these paralogs. Syntenic analysis suggested that the four Kissr paralogs arose through the two
rounds of whole genome duplication (1R and 2R) in early vertebrates, followed by multiple gene loss events in the
actinopterygian and sarcopterygian lineages. Due to gene loss there was no impact of the teleost-specific whole genome
duplication (3R) on the number of Kissr paralogs in current teleosts.
Domains
Life Sciences [q-bio]
Origin : Publication funded by an institution