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Mammalian puberty: a fly perspective

Mammalian puberty and Drosophila metamorphosis, despite their evolutionary distance, exhibit similar design principles and conservation of molecular components. In this Viewpoint, we review recent advances in this area and the similarities between both processes in terms of the signaling pathways an...

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Autores principales: Guirado, Juan, Carranza‐Valencia, Juan, Morante, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084137/
https://www.ncbi.nlm.nih.gov/pubmed/35607827
http://dx.doi.org/10.1111/febs.16534
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author Guirado, Juan
Carranza‐Valencia, Juan
Morante, Javier
author_facet Guirado, Juan
Carranza‐Valencia, Juan
Morante, Javier
author_sort Guirado, Juan
collection PubMed
description Mammalian puberty and Drosophila metamorphosis, despite their evolutionary distance, exhibit similar design principles and conservation of molecular components. In this Viewpoint, we review recent advances in this area and the similarities between both processes in terms of the signaling pathways and neuroendocrine circuits involved. We argue that the detection and uptake of peripheral fat by Drosophila prothoracic endocrine cells induces endomembrane remodeling and ribosomal maturation, leading to the acquisition of high biosynthetic and secretory capacity. The absence of this fat–neuroendocrine interorgan communication leads to giant, obese, non‐pupating larvae. Importantly, human leptin is capable of signaling the pupariation process in Drosophila, and its expression prevents obesity and triggers maturation in mutants that do not pupate. This implies that insect metamorphosis can be used to address issues related to the biology of leptin and puberty.
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spelling pubmed-100841372023-04-11 Mammalian puberty: a fly perspective Guirado, Juan Carranza‐Valencia, Juan Morante, Javier FEBS J Viewpoints Mammalian puberty and Drosophila metamorphosis, despite their evolutionary distance, exhibit similar design principles and conservation of molecular components. In this Viewpoint, we review recent advances in this area and the similarities between both processes in terms of the signaling pathways and neuroendocrine circuits involved. We argue that the detection and uptake of peripheral fat by Drosophila prothoracic endocrine cells induces endomembrane remodeling and ribosomal maturation, leading to the acquisition of high biosynthetic and secretory capacity. The absence of this fat–neuroendocrine interorgan communication leads to giant, obese, non‐pupating larvae. Importantly, human leptin is capable of signaling the pupariation process in Drosophila, and its expression prevents obesity and triggers maturation in mutants that do not pupate. This implies that insect metamorphosis can be used to address issues related to the biology of leptin and puberty. John Wiley and Sons Inc. 2022-06-21 2023-01 /pmc/articles/PMC10084137/ /pubmed/35607827 http://dx.doi.org/10.1111/febs.16534 Text en © 2022 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Viewpoints
Guirado, Juan
Carranza‐Valencia, Juan
Morante, Javier
Mammalian puberty: a fly perspective
title Mammalian puberty: a fly perspective
title_full Mammalian puberty: a fly perspective
title_fullStr Mammalian puberty: a fly perspective
title_full_unstemmed Mammalian puberty: a fly perspective
title_short Mammalian puberty: a fly perspective
title_sort mammalian puberty: a fly perspective
topic Viewpoints
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084137/
https://www.ncbi.nlm.nih.gov/pubmed/35607827
http://dx.doi.org/10.1111/febs.16534
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