Cryptochrome–Timeless structure reveals circadian clock timing mechanisms
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Abstract
Circadian rhythms influence many behaviours and diseases 1,2. They arise from oscillations in gene expression caused by repressor proteins that directly inhibit transcription of their own genes. The fly circadian clock offers a valuable model for studying these processes, wherein Timeless (Tim) plays a critical role in mediating nuclear entry of the transcriptional repressor Period (Per) and the photoreceptor Cryptochrome (Cry) entrains the clock by triggering Tim degradation in light 2,3. Here, through cryogenic electron microscopy of the Cry-Tim complex, we show how a light-sensing cryptochrome recognizes its target. Cry engages a continuous core of amino-terminal Tim armadillo repeats, resembling how photolyases recognize damaged DNA, and binds a C-terminal Tim helix, reminiscent of the interactions between light-insensitive cryptochromes and their partners in mammals. The structure highlights how the Cry flavin cofactor undergoes conformational changes that couple to large-scale rearrangements at the molecular interface, and how a phosphorylated segment in Tim may impact clock period by regulating the binding of Importin-α and the nuclear import of Tim-Per 4,5. Moreover, the structure reveals that the N terminus of Tim inserts into the restructured Cry pocket to replace the autoinhibitory C-terminal tail released by light, thereby providing a possible explanation for how the long-short Tim polymorphism adapts flies to different climates 6,7.
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- Authors
- Lin, C., Feng, S., DeOliveira, C. C., & Crane, B. R.
- Affiliations
- Cornell University (US)
- Corresponding author
- Crane, Brian R.
- Venue
- Nature
- Published
- 2023-04-26
- Volume
- 617
- Issue
- 7959
- Pages
- 194-199
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC11034853
- OpenAlex
- W4367049164
- Cited by
- 51
- References
- 68
- Citations by year
- 2026: 14 · 2025: 26 · 2024: 9 · 2023: 2
- FWCI
- 7.59
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- Locations
- Nature (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Science Foundation (1719875)
- National Institutes of Health (DMR-1719875, 1s10od017992-01)
- Cornell Center for Materials Research (DMR‐1719875, 1719875)
- National Institute of General Medical Sciences (R35GM122535)
- Division of Materials Research (DMR-1719875, 1719875)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Light effects on plants
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Keywords
- cryptochrome, TIMELESS, circadian clock, Drosophila, armadillo repeats, optical sensing, period, nuclear import, importin alpha, clock period, transcriptional repressor
- MeSH terms
- Animals, Circadian Rhythm, Drosophila melanogaster, Eye Proteins, Light, Mammals, Cryoelectron Microscopy, Active Transport, Cell Nucleus, alpha Karyopherins, Drosophila Proteins, Cryptochromes, Period Circadian Proteins, Circadian Clocks
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