Abstract

Circadian clocks prepare the organism to cyclic environmental changes in light, temperature, or food availability. Here, we characterized the master clock in the brain of a strongly photoperiodic insect, the aphid Acyrthosiphon pisum, immunohistochemically with antibodies against A. pisum Period (PER), Drosophila melanogaster Cryptochrome (CRY1), and crab Pigment-Dispersing Hormone (PDH). The latter antibody detects all so far known PDHs and PDFs (Pigment-Dispersing Factors), which play a dominant role in the circadian system of many arthropods. We found that, under long days, PER and CRY are expressed in a rhythmic manner in three regions of the brain: the dorsal and lateral protocerebrum and the lamina. No staining was detected with anti-PDH, suggesting that aphids lack PDF. All the CRY1-positive cells co-expressed PER and showed daily PER/CRY1 oscillations of high amplitude, while the PER oscillations of the CRY1-negative PER neurons were of considerable lower amplitude. The CRY1 oscillations were highly synchronous in all neurons, suggesting that aphid CRY1, similarly to Drosophila CRY1, is light sensitive and its oscillations are synchronized by light-dark cycles. Nevertheless, in contrast to Drosophila CRY1, aphid CRY1 was not degraded by light, but steadily increased during the day and decreased during the night. PER was always located in the nuclei of the clock neurons, while CRY was predominantly cytoplasmic and revealed the projections of the PER/CRY1-positive neurons. We traced the PER/CRY1-positive neurons through the aphid protocerebrum discovering striking similarities with the circadian clock of D. melanogaster: The CRY1 fibers innervate the dorsal and lateral protocerebrum and putatively connect the different PER-positive neurons with each other. They also run toward the pars intercerebralis, which controls hormone release via the neurohemal organ, the corpora cardiaca. In contrast to Drosophila, the CRY1-positive fibers additionally travel directly toward the corpora cardiaca and the close-by endocrine gland, corpora allata. This suggests a direct link between the circadian clock and the photoperiodic control of hormone release that can be studied in the future.

Highlights

  • Living beings evolved in a cyclic environment in which many factors, such as light, temperature, humidity, and food availability oscillate in a daily 24-h rhythm

  • Tracing the CRY-positive neurons in A. pisum, we found that some axons project to the pars intercerebralis and others to the corpora cardiaca/allata complex, the neuroendocrine system that secretes insulin-like peptides (ILPs) into the circulation (Nässel and Broeck, 2016) and produces and secretes Juvenile Hormone (Taguchi et al, 2017)

  • We will compare our results on the aphid clock with results gained for other insects, and at the end, we will discuss the possibility that the aphid clock makes connections to the photoperiodic system

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Summary

Introduction

Living beings evolved in a cyclic environment in which many factors, such as light, temperature, humidity, and food availability oscillate in a daily 24-h rhythm. In addition to controlling daily rhythms, the master clock is thought to serve as internal reference for measuring day length (Bünning, 1936; Shim et al, 2017; Wood et al, 2020; Saunders, 2021). The latter capability is important to anticipate and prepare in advance for seasonal changes in the environment, known as photoperiodic response. The involvement of the circadian clock in photoperiodic responses is established in various organisms from plant to mammals but, in insects, it is still an open question with intense controversy (Bradshaw and Holzapfel, 2017). The aim of this study was to characterize the neuronal network of the circadian clock in the brain of another strongly photoperiodic insect, the pea aphid Acyrthosiphon pisum

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