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Vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers

Wing polymorphism is an evolutionary feature found in a wide variety of insects, which offers a model system for studying the evolutionary significance of dispersal. In the wing-dimorphic planthopper Nilaparvata lugens, the insulin/insulin-like growth factor signaling (IIS) pathway acts as a ‘master...

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Autores principales: Zhang, Jin-Li, Fu, Sheng-Jie, Chen, Sun-Jie, Chen, Hao-Hao, Liu, Yi-Lai, Liu, Xin-Yang, Xu, Hai-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7899339/
https://www.ncbi.nlm.nih.gov/pubmed/33561165
http://dx.doi.org/10.1371/journal.pgen.1009312
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author Zhang, Jin-Li
Fu, Sheng-Jie
Chen, Sun-Jie
Chen, Hao-Hao
Liu, Yi-Lai
Liu, Xin-Yang
Xu, Hai-Jun
author_facet Zhang, Jin-Li
Fu, Sheng-Jie
Chen, Sun-Jie
Chen, Hao-Hao
Liu, Yi-Lai
Liu, Xin-Yang
Xu, Hai-Jun
author_sort Zhang, Jin-Li
collection PubMed
description Wing polymorphism is an evolutionary feature found in a wide variety of insects, which offers a model system for studying the evolutionary significance of dispersal. In the wing-dimorphic planthopper Nilaparvata lugens, the insulin/insulin-like growth factor signaling (IIS) pathway acts as a ‘master signal’ that directs the development of either long-winged (LW) or short-winged (SW) morphs via regulation of the activity of Forkhead transcription factor subgroup O (NlFoxO). However, downstream effectors of the IIS–FoxO signaling cascade that mediate alternative wing morphs are unclear. Here we found that vestigial (Nlvg), a key wing-patterning gene, is selectively and temporally regulated by the IIS–FoxO signaling cascade during the wing-morph decision stage (fifth-instar stage). RNA interference (RNAi)-mediated silencing of Nlfoxo increase Nlvg expression in the fifth-instar stage (the last nymphal stage), thereby inducing LW development. Conversely, silencing of Nlvg can antagonize the effects of IIS activity on LW development, redirecting wing commitment from LW to the morph with intermediate wing size. In vitro and in vivo binding assays indicated that NlFoxO protein may suppress Nlvg expression by directly binding to the first intron region of the Nlvg locus. Our findings provide a first glimpse of the link connecting the IIS pathway to the wing-patterning network on the developmental plasticity of wings in insects, and help us understanding how phenotypic diversity is generated by the modification of a common set of pattern elements.
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spelling pubmed-78993392021-03-02 Vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers Zhang, Jin-Li Fu, Sheng-Jie Chen, Sun-Jie Chen, Hao-Hao Liu, Yi-Lai Liu, Xin-Yang Xu, Hai-Jun PLoS Genet Research Article Wing polymorphism is an evolutionary feature found in a wide variety of insects, which offers a model system for studying the evolutionary significance of dispersal. In the wing-dimorphic planthopper Nilaparvata lugens, the insulin/insulin-like growth factor signaling (IIS) pathway acts as a ‘master signal’ that directs the development of either long-winged (LW) or short-winged (SW) morphs via regulation of the activity of Forkhead transcription factor subgroup O (NlFoxO). However, downstream effectors of the IIS–FoxO signaling cascade that mediate alternative wing morphs are unclear. Here we found that vestigial (Nlvg), a key wing-patterning gene, is selectively and temporally regulated by the IIS–FoxO signaling cascade during the wing-morph decision stage (fifth-instar stage). RNA interference (RNAi)-mediated silencing of Nlfoxo increase Nlvg expression in the fifth-instar stage (the last nymphal stage), thereby inducing LW development. Conversely, silencing of Nlvg can antagonize the effects of IIS activity on LW development, redirecting wing commitment from LW to the morph with intermediate wing size. In vitro and in vivo binding assays indicated that NlFoxO protein may suppress Nlvg expression by directly binding to the first intron region of the Nlvg locus. Our findings provide a first glimpse of the link connecting the IIS pathway to the wing-patterning network on the developmental plasticity of wings in insects, and help us understanding how phenotypic diversity is generated by the modification of a common set of pattern elements. Public Library of Science 2021-02-09 /pmc/articles/PMC7899339/ /pubmed/33561165 http://dx.doi.org/10.1371/journal.pgen.1009312 Text en © 2021 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zhang, Jin-Li
Fu, Sheng-Jie
Chen, Sun-Jie
Chen, Hao-Hao
Liu, Yi-Lai
Liu, Xin-Yang
Xu, Hai-Jun
Vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers
title Vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers
title_full Vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers
title_fullStr Vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers
title_full_unstemmed Vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers
title_short Vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers
title_sort vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7899339/
https://www.ncbi.nlm.nih.gov/pubmed/33561165
http://dx.doi.org/10.1371/journal.pgen.1009312
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