Insulin signaling as a mechanism underlying developmental plasticity: the role of FOXO in a nutritional polyphenism.

We investigated whether insulin signaling, known to mediate physiological plasticity in response to changes in nutrition, also facilitates discrete phenotypic responses such as polyphenisms. We test the hypothesis that the gene FOXO--which regulates growth arrest under nutrient stress--mediates a nu...

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Autores principales: Emilie C Snell-Rood, Armin P Moczek
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Publicado: Public Library of Science (PLoS) 2012
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Acceso en línea:https://doaj.org/article/d289ff7f118c4458857bc5a8a5d7af4c
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spelling oai:doaj.org-article:d289ff7f118c4458857bc5a8a5d7af4c2021-11-18T07:22:15ZInsulin signaling as a mechanism underlying developmental plasticity: the role of FOXO in a nutritional polyphenism.1932-620310.1371/journal.pone.0034857https://doaj.org/article/d289ff7f118c4458857bc5a8a5d7af4c2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22514679/?tool=EBIhttps://doaj.org/toc/1932-6203We investigated whether insulin signaling, known to mediate physiological plasticity in response to changes in nutrition, also facilitates discrete phenotypic responses such as polyphenisms. We test the hypothesis that the gene FOXO--which regulates growth arrest under nutrient stress--mediates a nutritional polyphenism in the horned beetle, Onthophagus nigriventris. Male beetles in the genus Onthophagus vary their mating strategy with body size: large males express horns and fight for access to females while small males invest heavily in genitalia and sneak copulations with females. Given that body size and larval nutrition are linked, we predicted that 1) FOXO expression would differentially scale with body size (nutritional status) between males and females, and 2) manipulation of FOXO expression would affect the nutritional polyphenism in horns and genitalia. First, we found that FOXO expression varied with body size in a tissue- and sex-specific manner, being more highly expressed in the abdominal tissue of large (horned) males, in particular in regions associated with genitalia development. Second, we found that knockdown of FOXO through RNA-interference resulted in the growth of relatively larger copulatory organs compared to control-injected individuals and significant, albeit modest, increases in relative horn length. Our results support the hypothesis that FOXO expression in the abdominal tissue limits genitalia growth, and provides limited support for the hypothesis that FOXO regulates relative horn length through direct suppression of horn growth. Both results support the idea that tissue-specific FOXO expression may play a general role in regulating scaling relationships in nutritional polyphenisms by signaling traits to be relatively smaller.Emilie C Snell-RoodArmin P MoczekPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 4, p e34857 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Emilie C Snell-Rood
Armin P Moczek
Insulin signaling as a mechanism underlying developmental plasticity: the role of FOXO in a nutritional polyphenism.
description We investigated whether insulin signaling, known to mediate physiological plasticity in response to changes in nutrition, also facilitates discrete phenotypic responses such as polyphenisms. We test the hypothesis that the gene FOXO--which regulates growth arrest under nutrient stress--mediates a nutritional polyphenism in the horned beetle, Onthophagus nigriventris. Male beetles in the genus Onthophagus vary their mating strategy with body size: large males express horns and fight for access to females while small males invest heavily in genitalia and sneak copulations with females. Given that body size and larval nutrition are linked, we predicted that 1) FOXO expression would differentially scale with body size (nutritional status) between males and females, and 2) manipulation of FOXO expression would affect the nutritional polyphenism in horns and genitalia. First, we found that FOXO expression varied with body size in a tissue- and sex-specific manner, being more highly expressed in the abdominal tissue of large (horned) males, in particular in regions associated with genitalia development. Second, we found that knockdown of FOXO through RNA-interference resulted in the growth of relatively larger copulatory organs compared to control-injected individuals and significant, albeit modest, increases in relative horn length. Our results support the hypothesis that FOXO expression in the abdominal tissue limits genitalia growth, and provides limited support for the hypothesis that FOXO regulates relative horn length through direct suppression of horn growth. Both results support the idea that tissue-specific FOXO expression may play a general role in regulating scaling relationships in nutritional polyphenisms by signaling traits to be relatively smaller.
format article
author Emilie C Snell-Rood
Armin P Moczek
author_facet Emilie C Snell-Rood
Armin P Moczek
author_sort Emilie C Snell-Rood
title Insulin signaling as a mechanism underlying developmental plasticity: the role of FOXO in a nutritional polyphenism.
title_short Insulin signaling as a mechanism underlying developmental plasticity: the role of FOXO in a nutritional polyphenism.
title_full Insulin signaling as a mechanism underlying developmental plasticity: the role of FOXO in a nutritional polyphenism.
title_fullStr Insulin signaling as a mechanism underlying developmental plasticity: the role of FOXO in a nutritional polyphenism.
title_full_unstemmed Insulin signaling as a mechanism underlying developmental plasticity: the role of FOXO in a nutritional polyphenism.
title_sort insulin signaling as a mechanism underlying developmental plasticity: the role of foxo in a nutritional polyphenism.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/d289ff7f118c4458857bc5a8a5d7af4c
work_keys_str_mv AT emiliecsnellrood insulinsignalingasamechanismunderlyingdevelopmentalplasticitytheroleoffoxoinanutritionalpolyphenism
AT arminpmoczek insulinsignalingasamechanismunderlyingdevelopmentalplasticitytheroleoffoxoinanutritionalpolyphenism
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