Neuropeptide Signaling: Unravelling the evolutionary history of kisspeptin

Experiments in sea cucumbers reveal how the physiological responses regulated by a neuropeptide called kisspeptin have evolved.
  1. Maria I Arnone  Is a corresponding author
  2. Paola Oliveri
  1. Department of Biology and Evolution of Marine Organisms, Stazione Zoologica Anton Dohrn, Italy
  2. Centre for Life’s Origins and Evolution, University College London, United Kingdom
  3. Research Department of Genetics, Evolution and Environment, University College London, United Kingdom

The world around us is constantly changing. As seasons shift, or as night turns to day, and food becomes more or less available, every organism must adapt their behavior and physiology to cope with its changing environment. The neuroendocrine systems play a central role in converting signals from the environment into biomolecules that can generate a response. Cells in these systems communicate by releasing various signals, including small proteins called neuropeptides. These molecules then travel towards their target cells where they bind to specific receptors and trigger a reaction that adjusts the physiology of cells and the tissues or organs they belong to (Tessmar-Raible, 2007).

A neuropeptide called kisspeptin is known to regulate fertility and reproduction in mammals (Hameed et al., 2011). The gene for kisspeptin is primarily expressed in the central nervous system, but is also active in other tissues such as the liver and heart. The gene that codes for its matching receptor shows a distinct but often overlapping pattern of expression (Bhattacharya and Babwah, 2015; Figure 1). Recent studies in adult mammals have revealed new physiological roles for this neuropeptide signaling system. For example, it has been shown that kisspeptin and its receptor regulate glucose homeostasis, feeding behavior and body mass composition by sending signals between the liver and pancreas (Wolfe and Hussain, 2018).

The role of kisspeptin in sea cucumbers and mammals.

Schematic showing the main organs that express kisspeptin (magenta) and/or its receptor (blue) in mammals (left panel) and sea cucumbers (right panel). The binding of kisspeptin (Kiss) to its receptor (KissR) triggers an intracellular pathway which sequentially activates the signaling molecules Ca2+/Gq/PLC/PKC/MAPK. This stimulates a molecule called ERK1/2 which regulates a number of cellular processes, including gene expression (center panel). Wang et al. showed that the signaling cascade triggered by kisspeptin regulates similar biological processes in mammals and sea cucumbers, such as reproduction, glucose metabolism and body mass.

Image credit: Maria I Arnone.

The genes for the neuropeptide kisspeptin and its receptor have also been identified in several marine invertebrates, including members of the echinoderm family, such as sea stars, sea urchins and sea cucumbers (Elphick et al., 2018). In sea urchins, it has been reported that the gene for kisspeptin is expressed in the gut of their larvae (Wood et al., 2018). However, we know relatively little about when and where this gene is expressed in other echinoderms or about its physiological role.

Now, in eLife, Naiming Zhou from Zhejiang University and co-workers – including Tianming Wang, Zheng Cao and Zhangfei Shen as joint first authors – report experiments identifying the location and role of the kisspeptin signaling system in the sea cucumber Apostichopus japonicus (Wang et al., 2020). This allowed the team (who are based in China and the US) to unravel the evolutionary history of this neuropeptide signaling system, which spans over more than 540 million years.

When studying the genome of A. japonicus, Wang et al. identified one gene which codes for two mature neuropeptides (AjKiss1a and AjKiss1b) and two genes which encode two receptor proteins (AjKissR1 and AjKissR2). In vitro experiments in cultured human cells showed that both neuropeptides are able to bind and specifically activate either receptor. Furthermore, the receptor proteins from sea cucumbers could also be activated by kisspeptin neuropeptides from other vertebrates, including humans.

Further experiments showed that when kisspeptin binds to either of the receptor proteins in human cells, this triggers an intracellular signaling pathway that eventually activates a molecule called MAPK (Castaño et al., 2009; Figure 1). These findings were further supported by in vivo experiments in the oocytes of sea cucumbers, in which the activation of MAPK was also detected following exposure to the neuropeptide AjKiss1b. This suggests that the molecular mechanisms activated by the kisspeptin signaling system are evolutionary conserved.

Next, Wang et al. studied the expression and physiological role of kisspeptin in adult sea cucumbers. This revealed that the precursor peptide for AjKiss1 is primarily expressed in the central nervous system (nerve ring) and gonads of A. japonicus, and its expression levels changed significantly during the reproductive season (Figure 1). The gene for the AjKiss1R1 receptor was also active in the nerve ring and gonads, in addition to other organs, including the muscles of the body-wall and respiratory tree that are only present in sea cucumbers (Spirina and Dolmatov, 2001).

When sea cucumbers were exposed to sustained high levels of the neuropeptide AjKiss1b, this upregulated the expression of proteins involved in the metabolism of glucose and induced a dormancy-like state known as aestivation: this is characterized by extensive weight loss and degeneration of the digestive tract. This suggests that, similar to vertebrates, the kisspeptin signaling system in sea cucumbers is also involved in regulating glucose metabolism, reproduction and body mass (Figure 1). The shared role of kisspeptin in vertebrates and sea cucumbers reveals important insights into how this neuropeptide signaling system evolved.

The findings of Wang et al. demonstrate how comparing the genomes and gene roles of different organisms can unravel new aspects of animal biology that may be useful for biomedical studies. Future studies on unexplored animals will shed further light on the complex interactions that allow organisms to adapt in response to their changing environment.

References

Article and author information

Author details

  1. Maria I Arnone

    Maria I Arnone is in the Department of Biology and Evolution of Marine Organisms, Stazione Zoologica Anton Dohrn, Naples, Italy

    For correspondence
    miarnone@szn.it
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-9012-7624
  2. Paola Oliveri

    Paola Oliveri is in the Centre for Life’s Origins and Evolution, and the Research Department of Genetics, Evolution and Environment, University College London, London, United Kingdom

    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-3477-8529

Publication history

  1. Version of Record published: June 15, 2020 (version 1)

Copyright

© 2020, Arnone and Oliveri

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 956
    views
  • 93
    downloads
  • 0
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Maria I Arnone
  2. Paola Oliveri
(2020)
Neuropeptide Signaling: Unravelling the evolutionary history of kisspeptin
eLife 9:e58599.
https://doi.org/10.7554/eLife.58599

Further reading

    1. Evolutionary Biology
    Case Vincent Miller, Jen A Bright ... Michael Pittman
    Research Article

    Enantiornithines were the dominant birds of the Mesozoic, but understanding of their diet is still tenuous. We introduce new data on the enantiornithine family Bohaiornithidae, famous for their large size and powerfully built teeth and claws. In tandem with previously published data, we comment on the breadth of enantiornithine ecology and potential patterns in which it evolved. Body mass, jaw mechanical advantage, finite element analysis of the jaw, and traditional morphometrics of the claws and skull are compared between bohaiornithids and living birds. We find bohaiornithids to be more ecologically diverse than any other enantiornithine family: Bohaiornis and Parabohaiornis are similar to living plant-eating birds; Longusunguis resembles raptorial carnivores; Zhouornis is similar to both fruit-eating birds and generalist feeders; and Shenqiornis and Sulcavis plausibly ate fish, plants, or a mix of both. We predict the ancestral enantiornithine bird to have been a generalist which ate a wide variety of foods. However, more quantitative data from across the enantiornithine tree is needed to refine this prediction. By the Early Cretaceous, enantiornithine birds had diversified into a variety of ecological niches like crown birds after the K-Pg extinction, adding to the evidence that traits unique to crown birds cannot completely explain their ecological success.

    1. Evolutionary Biology
    Mátyás Paczkó, Eörs Szathmáry, András Szilágyi
    Research Article

    The RNA world hypothesis proposes that during the early evolution of life, primordial genomes of the first self-propagating evolutionary units existed in the form of RNA-like polymers. Autonomous, non-enzymatic, and sustained replication of such information carriers presents a problem, because product formation and hybridization between template and copy strands reduces replication speed. Kinetics of growth is then parabolic with the benefit of entailing competitive coexistence, thereby maintaining diversity. Here, we test the information-maintaining ability of parabolic growth in stochastic multispecies population models under the constraints of constant total population size and chemostat conditions. We find that large population sizes and small differences in the replication rates favor the stable coexistence of the vast majority of replicator species (‘genes’), while the error threshold problem is alleviated relative to exponential amplification. In addition, sequence properties (GC content) and the strength of resource competition mediated by the rate of resource inflow determine the number of coexisting variants, suggesting that fluctuations in building block availability favored repeated cycles of exploration and exploitation. Stochastic parabolic growth could thus have played a pivotal role in preserving viable sequences generated by random abiotic synthesis and providing diverse genetic raw material to the early evolution of functional ribozymes.