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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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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. |
format | Online Article Text |
id | pubmed-7899339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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