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npj Metabolic Health and Disease· 2026Q1

The clock gene cycle synchronizes circadian metabolic oscillations uniquely in reproductively active Culex pipiens females

Mizuki Yoshida, Matthew Wolkoff, Cheolho Sim, Megan E. Meuti et al.

Short summary

Reproductively active female Culex pipiens mosquitoes exhibit 27 synchronized oscillating metabolites, significantly more than the 11 found in diapausing females, with the clock gene CYCLE being crucial for maintaining these oscillations.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Reproductively active female Culex pipiens have 27 synchronized oscillating metabolites, while diapausing females have only 11.
  • The clock gene CYCLE is essential for maintaining synchronized metabolic oscillations.
  • Loss of CYCLE function disrupts metabolic oscillations in mosquitoes under both long and short day conditions.
  • This is the first study to compare oscillating metabolites between diapausing and non-diapausing Culex pipiens.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract The circadian clock regulates changes in daily metabolite abundance, coordinating animal activity, feeding and rest. The Northern house mosquito, Culex pipiens , also displays seasonal changes between periods of reproductive activity and overwintering diapause, regulated by changes in daylength. However, differences in metabolic oscillations between diapause and non-diapause have yet to be characterized. We hypothesized that reproductively active, non-diapausing mosquitoes would show large metabolic oscillations compared to diapausing mosquitoes. Our previous work demonstrated that CYCLE regulates insulin signaling, reproductive growth and olfaction, and that knocking out cycle causes a diapause-like state regardless of photoperiod, thus we predicted large-scale disruptions to the daily and seasonal metabolomes of CpCyc −/− mosquitoes. We identified 27 metabolites showing highly synchronized oscillations in non-diapausing wildtype (WT) females, but only 11 oscillating metabolites in WT diapausing females. We also observed large-scale metabolic disruptions in CpCyc −/− females reared under both long and short days, especially a loss of synchronicity between oscillations. This is the first report on differences in oscillating metabolites between diapausing and non-diapausing Cx. pipiens , and the impact of cycle on oscillating metabolites. This provides additional mechanistic insights as to how the circadian clock regulates daily and seasonal metabolic differences, with implications for insulin dysregulation and metabolic disorders.

The authors' abstract, as published at the source. npj Metabolic Health and Disease, 2026 · DOI ↗

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Field: Endocrine and Autonomic Systems

Endocrine and Autonomic SystemsNeuroscience