# The Evolutionary Flexibility of the Drosophila Circadian Clock: Network Constraints or Adaptive Freedom?

**Authors:** Leo Douglas Creasey, Petar Borisov Petrov, Eran Tauber

PMC · DOI: 10.1093/gbe/evag061 · Genome Biology and Evolution · 2026-03-07

## TL;DR

This study examines how the circadian clock in fruit flies evolves, finding that it allows for flexibility rather than strict constraints.

## Contribution

The study provides new insights into the evolutionary flexibility of the Drosophila circadian clock network.

## Key findings

- Clk and per show high nucleotide divergence, while Pdp1 and sgg show little evolutionary change.
- 67 co-evolving site pairs were identified among CLK-PER, CLK-CWO, and SGG-PER.
- Four genes (cwo, jet, per, and sgg) show evidence of positive selection.

## Abstract

The study of network evolution is critical to understanding how complex biological processes arise and adapt over time. Protein networks, composed of interacting components, can exhibit varying degrees of conservation and flexibility, enabling organisms to fine-tune their responses to environmental changes. Using the circadian clock system in Drosophila as a case study, we explore how such networks evolve. We leverage the recently published 101 Drosophilidae genome project to analyze the evolution and co-evolution of 11 core clock proteins across 65 species spanning about 60 million years of evolution. A sliding window analysis of coding regions reveals substantial heterogeneity in nucleotide divergence, with Clk and per exhibiting high divergence, whereas Pdp1 and sgg show virtually no evolutionary change. Additionally, we assessed interdependent amino acid evolution across different proteins, identifying 67 co-evolving site pairs, primarily among CLK-PER, CLK-CWO, and SGG-PER. Using codon-based models of evolution, we found four genes (cwo, jet, per, and sgg) showing evidence of positive selection. Since several clock proteins are pleiotropic, we tested whether their multifunctionality influences their evolutionary constraints. Using alternative approaches to assess pleiotropy, we found no significant correlation between pleiotropy and the nonsynonymous substitution rate (Ka) in 440 Drosophila proteins, including circadian clock ones. Overall, our findings suggest that the circadian clock network does not impose strong constraints on the evolution of its components. This flexibility may facilitate species-specific adaptation of the clock and allow the pleiotropic functions of clock proteins.

## Linked entities

- **Genes:** CLK1 (CDC like kinase 1) [NCBI Gene 1195], PER1 (period circadian regulator 1) [NCBI Gene 5187], PDP1 (pyruvate dehydrogenase phosphatase catalytic subunit 1) [NCBI Gene 54704], sgg (shaggy) [NCBI Gene 31248], cwo (clockwork orange) [NCBI Gene 44669], FBXL15 (F-box and leucine rich repeat protein 15) [NCBI Gene 79176], CLK1 (CDC like kinase 1) [NCBI Gene 1195], PER1 (period circadian regulator 1) [NCBI Gene 5187], cwo (clockwork orange) [NCBI Gene 44669], sgg (shaggy) [NCBI Gene 31248]
- **Proteins:** CLK1 (CDC like kinase 1), PER1 (period circadian regulator 1), PDP1 (pyruvate dehydrogenase phosphatase catalytic subunit 1), sgg (shaggy), cwo (clockwork orange), sgg (shaggy)
- **Species:** Drosophila (taxon 7215), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Clk (Clock) [NCBI Gene 38872] {aka CG7391, CLOCK, Dmel\CG7391, Jerk, Jrk, PAS1}, sgg (shaggy) [NCBI Gene 31248] {aka CG2621, DMSGG3, DMZ3K25Z, Dm Zw3, Dmel\CG2621, Dmsgg3}, Pdp1 (PAR-domain protein 1) [NCBI Gene 45588] {aka CG17888, DM1, DM32, Dmel\CG17888, PDP, PDP-1epsilon}, cwo (clockwork orange) [NCBI Gene 44669] {aka AAF24476.1, CG17100, Dmel\CG17100, GM05287, bHLHe49, dcwo}, jet (jetlag) [NCBI Gene 33705] {aka CG8873, Dmel\CG8873, FBXL15, JETLAG}
- **Species:** Drosophila melanogaster (fruit fly, species) [taxon 7227]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13011797/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC13011797/full.md

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Source: https://tomesphere.com/paper/PMC13011797