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Details

Autor(en) / Beteiligte
Titel
Vestigial mediates the effect of insulin signaling pathway on wing-morph switching in planthoppers
Ist Teil von
  • PLoS genetics, 2021-02, Vol.17 (2), p.e1009312-e1009312
Ort / Verlag
United States: Public Library of Science
Erscheinungsjahr
2021
Quelle
EZB Free E-Journals
Beschreibungen/Notizen
  • 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.
Sprache
Englisch
Identifikatoren
ISSN: 1553-7404, 1553-7390
eISSN: 1553-7404
DOI: 10.1371/JOURNAL.PGEN.1009312
Titel-ID: cdi_plos_journals_2501878434

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