Regulation of forkhead box O transcription factor by insulin signaling pathway controls the reproductive diapause of the lady beetle, Coccinella septempunctata

Jun jie Chen, Xiao xiao Liu, Peng hui Guo, Nicholas M. Teets, Jin Cheng Zhou, Wan bin Chen, Qiao zhi Luo, Nipapan Kanjana, Yu yan Li, Li sheng Zhang

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

In biological control programs, knowledge about diapause regulation in natural enemy insects provides important insight for improving long-term storage, transportation, and field adoption of these biological control agents. As a natural predator of agricultural pests, the lady beetle Coccinella septempunctata has been commercially mass-cultured and widely employed in pest management. In some insects, insulin signaling, in conjunction with the downstream transcription factor Forkhead box O (FoxO), are master regulators of multiple physiological processes involved in diapause, but it is unclear whether insulin signaling and FoxO affect the diapause of C. septempunctata. In this study, we use a combination of approaches to demonstrate that insulin signaling and FoxO mediate the diapause response in C. septempunctata. In diapausing beetles, application of exogenous insulin and knocking down expression of CsFoxo with RNA interference (RNAi) both rescued beetles from developmental arrest. In non-diapausing beetles, knocking down expression of the insulin receptor (CsInR) with RNA interference (RNAi) arrested ovarian development and decreased juvenile hormone (JH) content to levels comparable to the diapause state. Taken together, these results suggest that a shutdown of insulin signaling prompts the activation of the downstream FoxO gene, leading to the diapause phenotype.

Original languageEnglish
Article number128104
JournalInternational Journal of Biological Macromolecules
Volume258
DOIs
StatePublished - Feb 2024

Bibliographical note

Publisher Copyright:
© 2023

Keywords

  • Diapause regulation
  • Forkhead box O
  • Insulin receptor

ASJC Scopus subject areas

  • Structural Biology
  • Biochemistry
  • Molecular Biology

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