Cargando…

Mechanisms regulating nutrition-dependent developmental plasticity through organ-specific effects in insects

Nutrition, via the insulin/insulin-like growth factor (IIS)/Target of Rapamycin (TOR) signaling pathway, can provide a strong molding force for determining animal size and shape. For instance, nutrition induces a disproportionate increase in the size of male horns in dung and rhinoceros beetles, or...

Descripción completa

Detalles Bibliográficos
Autores principales: Koyama, Takashi, Mendes, Cláudia C., Mirth, Christen K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783933/
https://www.ncbi.nlm.nih.gov/pubmed/24133450
http://dx.doi.org/10.3389/fphys.2013.00263
_version_ 1782285745653809152
author Koyama, Takashi
Mendes, Cláudia C.
Mirth, Christen K.
author_facet Koyama, Takashi
Mendes, Cláudia C.
Mirth, Christen K.
author_sort Koyama, Takashi
collection PubMed
description Nutrition, via the insulin/insulin-like growth factor (IIS)/Target of Rapamycin (TOR) signaling pathway, can provide a strong molding force for determining animal size and shape. For instance, nutrition induces a disproportionate increase in the size of male horns in dung and rhinoceros beetles, or mandibles in staghorn or horned flour beetles, relative to body size. In these species, well-fed male larvae produce adults with greatly enlarged horns or mandibles, whereas males that are starved or poorly fed as larvae bear much more modest appendages. Changes in IIS/TOR signaling plays a key role in appendage development by regulating growth in the horn and mandible primordia. In contrast, changes in the IIS/TOR pathway produce minimal effects on the size of other adult structures, such as the male genitalia in fruit flies and dung beetles. The horn, mandible and genitalia illustrate that although all tissues are exposed to the same hormonal environment within the larval body, the extent to which insulin can induce growth is organ specific. In addition, the IIS/TOR pathway affects body size and shape by controlling production of metamorphic hormones important for regulating developmental timing, like the steroid molting hormone ecdysone and sesquiterpenoid hormone juvenile hormone. In this review, we discuss recent results from Drosophila and other insects that highlight mechanisms allowing tissues to differ in their sensitivity to IIS/TOR and the potential consequences of these differences on body size and shape.
format Online
Article
Text
id pubmed-3783933
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-37839332013-10-16 Mechanisms regulating nutrition-dependent developmental plasticity through organ-specific effects in insects Koyama, Takashi Mendes, Cláudia C. Mirth, Christen K. Front Physiol Physiology Nutrition, via the insulin/insulin-like growth factor (IIS)/Target of Rapamycin (TOR) signaling pathway, can provide a strong molding force for determining animal size and shape. For instance, nutrition induces a disproportionate increase in the size of male horns in dung and rhinoceros beetles, or mandibles in staghorn or horned flour beetles, relative to body size. In these species, well-fed male larvae produce adults with greatly enlarged horns or mandibles, whereas males that are starved or poorly fed as larvae bear much more modest appendages. Changes in IIS/TOR signaling plays a key role in appendage development by regulating growth in the horn and mandible primordia. In contrast, changes in the IIS/TOR pathway produce minimal effects on the size of other adult structures, such as the male genitalia in fruit flies and dung beetles. The horn, mandible and genitalia illustrate that although all tissues are exposed to the same hormonal environment within the larval body, the extent to which insulin can induce growth is organ specific. In addition, the IIS/TOR pathway affects body size and shape by controlling production of metamorphic hormones important for regulating developmental timing, like the steroid molting hormone ecdysone and sesquiterpenoid hormone juvenile hormone. In this review, we discuss recent results from Drosophila and other insects that highlight mechanisms allowing tissues to differ in their sensitivity to IIS/TOR and the potential consequences of these differences on body size and shape. Frontiers Media S.A. 2013-09-26 /pmc/articles/PMC3783933/ /pubmed/24133450 http://dx.doi.org/10.3389/fphys.2013.00263 Text en Copyright © 2013 Koyama, Mendes and Mirth. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Koyama, Takashi
Mendes, Cláudia C.
Mirth, Christen K.
Mechanisms regulating nutrition-dependent developmental plasticity through organ-specific effects in insects
title Mechanisms regulating nutrition-dependent developmental plasticity through organ-specific effects in insects
title_full Mechanisms regulating nutrition-dependent developmental plasticity through organ-specific effects in insects
title_fullStr Mechanisms regulating nutrition-dependent developmental plasticity through organ-specific effects in insects
title_full_unstemmed Mechanisms regulating nutrition-dependent developmental plasticity through organ-specific effects in insects
title_short Mechanisms regulating nutrition-dependent developmental plasticity through organ-specific effects in insects
title_sort mechanisms regulating nutrition-dependent developmental plasticity through organ-specific effects in insects
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783933/
https://www.ncbi.nlm.nih.gov/pubmed/24133450
http://dx.doi.org/10.3389/fphys.2013.00263
work_keys_str_mv AT koyamatakashi mechanismsregulatingnutritiondependentdevelopmentalplasticitythroughorganspecificeffectsininsects
AT mendesclaudiac mechanismsregulatingnutritiondependentdevelopmentalplasticitythroughorganspecificeffectsininsects
AT mirthchristenk mechanismsregulatingnutritiondependentdevelopmentalplasticitythroughorganspecificeffectsininsects