Warming Up Your Tick-Tock: Temperature-Dependent Regulation of Circadian Clocks
Abstract
Circadian clocks are endogenous time-keeping mechanisms to adaptively coordinate animal behaviors and physiology with daily environmental changes. So far many circadian studies in model organisms have identified evolutionarily conserved molecular frames of circadian clock genes in the context of transcription–translation feedback loops. The molecular clockwork drives cell-autonomously cycling gene expression with ~24-hour periodicity, which is fundamental to circadian rhythms. Light and temperature are two of the most potent external time cues to reset the circadian phase of the internal clocks, yet relatively little is known about temperature-relevant clock regulation. In this review, we describe recent findings on temperature-dependent clock mechanisms in homeothermic mammals as compared with poikilothermic Drosophila at molecular, neural, and organismal levels. We propose thermodynamic transitions in RNA secondary structures might have been potent substrates for the molecular evolution of temperature-relevant post-transcriptional mechanisms. Future works should thus validate the potential involvement of specific post-transcriptional steps in temperature-dependent plasticity of circadian clocks.
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Temperature-dependent polyadenylation through RBM3, a cold-inducible RNA-binding protein, has been suggested to contribute to cell reprogramming during a stress response.
“Temperature-dependent polyadenylation through RBM3, a cold-inducible RNA-binding protein, has been suggested to contribute to cell reprogramming during a stress response55,56.”
From Diurnal rhythms of wrist temperature are associated with future disease risk in the UK Biobank (2023) · cites this paper as [55]
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- Authors
- Ki, Y., Ri, H., Lee, H., Yoo, E., Choe, J., & Lim, C.
- Affiliations
- Ulsan National Institute of Science and Technology (KR)
- Korea Advanced Institute of Science and Technology (KR)
- Corresponding author
- Lim, Chunghun
- Venue
- The Neuroscientist
- Publisher
- SAGE Publications
- Published
- 2015-03-17
- Volume
- 21
- Issue
- 5
- Pages
- 503-518
- ISSN
- 1073-8584 (ISSN-L)
- 1089-4098
- OpenAlex
- W2143954319
- Cited by
- 24
- References
- 76
- Citations by year
- 2024: 3 · 2023: 1 · 2022: 1 · 2021: 4 · 2020: 2 · 2019: 3 · 2018: 1 · 2017: 3 · 2016: 4 · 2015: 2
- FWCI
- 0.36
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Neuroscientist (publishedVersion)
- PubMed (publishedVersion)
- Scholarworks@UNIST (Ulsan National Institute of Science and Technology) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Physical Sciences › Environmental Science › Ecology › Physiological and biochemical adaptations
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- circadian clock, post-transcriptional regulation, RNA secondary structure, thermodynamic transitions, transcription-translation feedback loop, clock genes, Drosophila, mammals, circadian plasticity
- MeSH terms
- Animals, Circadian Rhythm, Environment, Humans, Mammals, Temperature, Gene Expression, Circadian Clocks
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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