How new communication behaviors evolve: Androgens as modifiers of neuromotor structure and function in foot-flagging frogs.

Androgen receptor Communication Evolutionary endocrinology Foot-flagging frog Sexual behavior Testosterone

Journal

Hormones and behavior
ISSN: 1095-6867
Titre abrégé: Horm Behav
Pays: United States
ID NLM: 0217764

Informations de publication

Date de publication:
20 Feb 2024
Historique:
received: 03 08 2023
revised: 08 12 2023
accepted: 05 02 2024
medline: 22 2 2024
pubmed: 22 2 2024
entrez: 21 2 2024
Statut: aheadofprint

Résumé

How diverse animal communication signals have arisen is a question that has fascinated many. Xenopus frogs have been a model system used for three decades to reveal insights into the neuroendocrine mechanisms and evolution of vocal diversity. Due to the ease of studying central nervous system control of the laryngeal muscles in vitro, Xenopus has helped us understand how variation in vocal communication signals between sexes and between species is produced at the molecular, cellular, and systems levels. Yet, it is becoming easier to make similar advances in non-model organisms. In this paper, we summarize our research on a group of frog species that have evolved a novel hind limb signal known as 'foot flagging.' We have previously shown that foot flagging is androgen dependent and that the evolution of foot flagging in multiple unrelated species is accompanied by the evolution of higher androgen hormone sensitivity in the leg muscles. Here, we present new preliminary data that compare patterns of androgen receptor expression and neuronal cell density in the lumbar spinal cord - the neuromotor system that controls the hind limb - between foot-flagging and non-foot-flagging frog species. We then relate our work to prior findings in Xenopus, highlighting which patterns of hormone sensitivity and neuroanatomical structure are shared between the neuromotor systems underlying Xenopus vocalizations and foot-flagging frogs' limb movement and which appear to be species-specific. Overall, we aim to illustrate the power of drawing inspiration from experiments in model organisms, in which the mechanistic details have been worked out, and then applying these ideas to a non-model species to reveal new details, further complexities, and fresh hypotheses.

Identifiants

pubmed: 38382227
pii: S0018-506X(24)00027-8
doi: 10.1016/j.yhbeh.2024.105502
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105502

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Auteurs

Lisa A Mangiamele (LA)

Department of Biological Sciences, Smith College, Northampton, MA 01063, United States of America. Electronic address: lmangiamele@smith.edu.

AllexAndrya Dawn (A)

Department of Biological Sciences, Smith College, Northampton, MA 01063, United States of America.

Kerry M LeCure (KM)

Department of Biological Sciences, Smith College, Northampton, MA 01063, United States of America.

Gina E Mantica (GE)

Department of Biological Sciences, Smith College, Northampton, MA 01063, United States of America.

Riccardo Racicot (R)

Department of Biological Sciences, Smith College, Northampton, MA 01063, United States of America.

Matthew J Fuxjager (MJ)

Department of Ecology and Evolutionary Biology, Brown University, Providence, RI 02912, United States of America.

Doris Preininger (D)

Department of Evolutionary Biology, University of Vienna, Vienna, Austria; Vienna Zoo, Vienna, Austria.

Classifications MeSH