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Updated: Nov 16, 2025

Determination of Reproductive Competence by Confirming Pubertal Onset and Performing a Fertility Assay in Mice and Rats
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Timing the Juvenile-Adult Neurohormonal Transition: Functions and Evolution.

Celia G Barredo1, Beatriz Gil-Marti1, Derya Deveci2

  • 1Molecular Physiology of Behavior Laboratory, Department of Molecular, Cellular and Developmental Neurobiology, Cajal Institute, Spanish National Research Council (CSIC), Madrid, Spain.

Frontiers in Endocrinology
|March 1, 2021
PubMed
Summary
This summary is machine-generated.

Reproductive maturation in mammals and insects may share a common evolutionary origin. Key neuroendocrine circuits regulating developmental transitions like puberty and metamorphosis could be ancient, challenging previous convergent evolution theories.

Keywords:
DrosophilaUrbilateriajuvenile-adult transitionmetamorphosisneuro-hormonal regulationneuroendocrine axispubertysleep

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Area of Science:

  • Developmental Biology
  • Evolutionary Biology
  • Neuroendocrinology

Background:

  • Puberty and metamorphosis are critical developmental transitions.
  • Neuroendocrine circuitry in the brain times these transitions in vertebrates.
  • These pathways also influence metabolism, sleep, and behavior.

Purpose of the Study:

  • To investigate the evolutionary origins of neuroendocrine axes regulating juvenile-to-adult transitions.
  • To challenge the notion that these pathways evolved convergently in mammals and insects.
  • To explore the potential presence of these circuits in the common bilaterian ancestor, Urbilateria.

Main Methods:

  • Comparative analysis of neuroendocrine signaling pathways across different species.
  • Examination of genetic networks involved in developmental transitions.
  • Phylogenetic reconstruction to infer evolutionary relationships of neuroendocrine circuits.

Main Results:

  • Recent findings suggest that neuroendocrine circuits regulating developmental transitions may not be analogous but homologous.
  • Evidence points to the presence of these circuits in the ancient bilaterian ancestor (Urbilateria).
  • Initial signaling pathways appear to have a single evolutionary origin, with conserved functions.

Conclusions:

  • The regulation of puberty and metamorphosis might stem from a shared evolutionary history, not just convergent evolution.
  • Conserved molecular players and co-opted genetic networks highlight the deep evolutionary roots of developmental timing.
  • Understanding these ancient circuits provides insights into conserved biological processes across diverse species.