Abstract

In mammals, neurokinin B (NKB) is a short peptide encoded by the gene tac3. It is involved in the brain control of reproduction by stimulating gonadotropin-releasing hormone (GnRH) neurons, mainly via kisspeptin. We investigated tac3 genes and peptides in a basal teleost, the European eel, which shows an atypical blockade of the sexual maturation at a prepubertal stage. Two tac3 paralogous genes (tac3a and tac3b) were identified in the eel genome, each encoding two peptides (NKBa or b and NKB-related peptide NKB-RPa or b). Amino acid sequence of eel NKBa is identical to human NKB, and the three others are novel peptide sequences. The four eel peptides present the characteristic C-terminal tachykinin sequence, as well as a similar alpha helix 3D structure. Tac3 genes were identified in silico in 52 species of vertebrates, and a phylogeny analysis was performed on the predicted TAC3 pre-pro-peptide sequences. A synteny analysis was also done to further assess the evolutionary history of tac3 genes. Duplicated tac3 genes in teleosts likely result from the teleost-specific whole genome duplication (3R). Among teleosts, TAC3b precursor sequences are more divergent than TAC3a, and a loss of tac3b gene would have even occurred in some teleost lineages. NKB-RP peptide, encoded beside NKB by tac3 gene in actinopterygians and basal sarcopterygians, would have been lost in ancestral amniotes. Tissue distribution of eel tac3a and tac3b mRNAs showed major expression of both transcripts in the brain especially in the diencephalon, as analyzed by specific qPCRs. Human NKB has been tested in vitro on primary culture of eel pituitary cells. Human NKB dose-dependently inhibited the expression of lhβ, while having no effect on other glycoprotein hormone subunits (fshβ, tshβ, and gpα) nor on gh. Human NKB also dose-dependently inhibited the expression of GnRH receptor (gnrh-r2). The four eel peptides have been synthesized and also tested in vitro. They all inhibited the expression of both lhβ and of gnrh-r2. This reveals a potential dual inhibitory role of the four peptides encoded by the two tac3 genes in eel reproduction, exerted at the pituitary level on both luteinizing hormone and GnRH receptor.

Highlights

  • Tachykinins are peptides mainly produced by brain and gut in mammals [for reviews see Ref. (1, 2)]

  • Using European eel specific tac3a primers designed on eel tac3a predicted genomic sequence, and tac3b primers designed on eel tac3b predicted genomic sequence (Table S2 in Supplementary Material), PCRs were performed on brain cDNAs

  • BLASTN analyses performed on the European eel draft genome, using the present tac3a and tac3b cloned sequences as queries, revealed that each transcript is encoded by 7 exons

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Summary

Introduction

Tachykinins are peptides mainly produced by brain and gut in mammals [for reviews see Ref. (1, 2)]. The most known tachykinin peptides are neurokinin A (NKA), substance P (SP), and neurokinin B (NKB). While NKA and SP are encoded by the tac[1] gene ( named preprotachykinin A gene, PPT-A, or PPT-I), NKB is coded by the tac[3] gene ( named PPT-B or PPT-II, and tac[2] in rodents) [for reviews see Ref. A second peptide encoded by the tac[3] gene has been recently found in teleosts and was either named neurokinin F (NKF) [zebrafish, Danio rerio (5)] or NKB-related peptide (NKB-RP) [grass carp, Ctenopharyngodon idella (6); tilapia, Oreochromis niloticus (7)]. A tac[4] gene ( named PPT-C or PPT-III) encodes other tachykinins in mammals: hemokinin-1 and endokinins [for reviews see Ref. An evolutionary scenario is that an ancestral gene has given rise to four tac genes after the two whole genome duplication rounds (1R/2R) in early vertebrates followed by the loss of one of the four paralogs (tac2) (9, 10)

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