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Kisspeptin-10

KP-10, Metastin (45-54), Kisspeptin-10 (human), KiSS-1

Quick Stats
Studies 877
Trials 47
Score 2
2011 pubmed 69 citations

Gene structure analysis of kisspeptin-2 (Kiss2) in the Senegalese sole (Solea senegalensis): characterization of two splice variants of Kiss2, and novel evidence for metabolic regulation of kisspeptin signaling in non-mammalian species.

Mechaly. Alejandro S AS; Viñas. Jordi J; Piferrer. Francesc F

Key Findings

  • Only the Kiss2 form of kisspeptin is present in Senegalese sole, existing as two splice variants: a functional version (Kiss2_v1) and a truncated non‑functional version (Kiss2_v2).
  • Fasting in the fish raises hypothalamic mRNA levels of the functional Kiss2_v1, a response opposite to what’s seen in mammals.
  • The rise in Kiss2_v1 during fasting is accompanied by increased pituitary LH and FSH mRNA, suggesting a metabolic control pathway for reproduction.

Practical Outcomes

  • The results hint that nutritional state can affect kisspeptin signaling, so timing of kisspeptin‑based interventions might matter. However, because the work is in fish, direct recommendations for human dosing or protocols are speculative.

Summary

This fish study found that the sole has two versions of the kisspeptin gene – one that works and one that doesn’t – and that when the fish fasts, the working version goes up in the brain and triggers higher reproductive hormone signals, linking food status to reproduction.

Abstract

Kisspeptin signaling in the brain is involved in the control of the onset of puberty in vertebrates. In this study, we present novel evidence indicating that kisspeptin may link energy balance and reproduction. For that purpose, we determined the complete gene structure of kisspeptin in a teleost fish, the Senegalese sole (Ss). In contrast to the situation evident in several fish, in this species only Kiss2 was found. Yet, two Ss Kiss2 isoforms generated by alternative splicing through intronic retention were detected: Ss Kiss2_v1, producing the functional protein, and Ss Kiss2_v2, coding for a truncated, non-functional protein. Specific qPCRs showed that the expression of these two isoforms varied differently in brain and gonads throughout maturation. In addition, and in contrast to what has been observed in mammals, fasting increased hypothalamic mRNA levels of Ss Kiss2_v1, which also caused a concomitant rise in pituitary Ss LH and Ss FSH mRNA. Together, these data indicate the impact of the nutritional status on Kiss mRNA expression as a potential regulatory mechanism for the metabolic control of reproduction in non-mammalian species, albeit with some significant differences with respect to the situation described in mammals.

Study Information

Provider

pubmed

Year

2011

Date

2011-03-31T00:00:00.000Z

DOI

10.1016/j.mce.2011.03.004

Citations

69

References

72