Abstract

BackgroundCircadian clocks allow organisms to anticipate daily fluctuations in their environment by driving rhythms in physiology and behavior. Inter-organismal differences in daily rhythms, called chronotypes, exist and can shift with age. In ants, age, caste-related behavior and chronotype appear to be linked. Brood-tending nurse ants are usually younger individuals and show “around-the-clock” activity. With age or in the absence of brood, nurses transition into foraging ants that show daily rhythms in activity. Ants can adaptively shift between these behavioral castes and caste-associated chronotypes depending on social context. We investigated how changes in daily gene expression could be contributing to such behavioral plasticity in Camponotus floridanus carpenter ants by combining time-course behavioral assays and RNA-Sequencing of forager and nurse brains.ResultsWe found that nurse brains have three times fewer 24 h oscillating genes than foragers. However, several hundred genes that oscillated every 24 h in forager brains showed robust 8 h oscillations in nurses, including the core clock genes Period and Shaggy. These differentially rhythmic genes consisted of several components of the circadian entrainment and output pathway, including genes said to be involved in regulating insect locomotory behavior. We also found that Vitellogenin, known to regulate division of labor in social insects, showed robust 24 h oscillations in nurse brains but not in foragers. Finally, we found significant overlap between genes differentially expressed between the two ant castes and genes that show ultradian rhythms in daily expression.ConclusionThis study provides a first look at the chronobiological differences in gene expression between forager and nurse ant brains. This endeavor allowed us to identify a putative molecular mechanism underlying plastic timekeeping: several components of the ant circadian clock and its output can seemingly oscillate at different harmonics of the circadian rhythm. We propose that such chronobiological plasticity has evolved to allow for distinct regulatory networks that underlie behavioral castes, while supporting swift caste transitions in response to colony demands. Behavioral division of labor is common among social insects. The links between chronobiological and behavioral plasticity that we found in C. floridanus, thus, likely represent a more general phenomenon that warrants further investigation.

Highlights

  • Circadian clocks allow organisms to anticipate daily fluctuations in their environment by driving rhythms in physiology and behavior

  • Looking for oscillating genes among the differentially expressed genes (DEGs) that we identified in C. floridanus, we found that more than one-third (i.e., 28 of the 81 DEGs) were expressed rhythmically in either forager or nurse brains (Fig. 6)

  • The peak expression of the 24 h cycling venom-carboxylesterase-6 in nurse brains was around ZT12-14, which corresponds to the peak time of colony foraging that we found in C. floridanus (Fig. 1, Additional File 4 and 6)

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Summary

Introduction

Circadian clocks allow organisms to anticipate daily fluctuations in their environment by driving rhythms in physiology and behavior. Living organisms exhibit adaptive rhythms in physiology and behavior as a way to anticipate predictable daily fluctuations in their environment [1,2,3]. Such daily rhythms are ubiquitous and have been discovered in both unicellular and multicellular organisms [4,5,6,7,8,9], including eusocial Hymenopterans such as ants and bees [10,11,12,13,14,15,16]. A more thorough molecular understanding of the Hymenopteran clock and its role in the social organization of insect colonies is needed to confirm this

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