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

• Published in: International journal of biological macromolecules 2024-02, Vol.258 (Pt 1), p.128104-128104, Article 128104
• Main Authors: Chen, Jun-jie, Liu, Xiao-xiao, Guo, Peng-hui, Teets, Nicholas M., Zhou, Jin-Cheng, Chen, Wan-bin, Luo, Qiao-zhi, Kanjana, Nipapan, Li, Yu-yan, Zhang, Li-sheng
• Format: Article
• Language: English
• Subjects: Diapause regulation; Forkhead box O; Insulin receptor
• ISSN: 0141-8130; 1879-0003
• DOI: 10.1016/j.ijbiomac.2023.128104

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. •The shutdown of insulin signaling prompts the activation of the downstream FoxO gene, leading to the diapause phenotype.•Under a long day photoperiod, insulin signaling leads to the suppression of FoxO gene and production of the JH.•In response to short day lengths, the insulin signaling pathway is shut down, thereby releasing the suppression of FoxO gene.