The degree of precision and accuracy with which the expression and activity of core clock genes and their protein products maintain their programmed 24-hour oscillatory cycle within individual cells and across entire organ systems. High fidelity indicates a robust, stable internal clock with clear peaks and troughs, essential for coordinating all downstream physiological rhythms. Loss of fidelity is a hallmark of circadian disruption and a contributor to biological aging.
Origin
This is a specialized term from molecular chronobiology, combining “Molecular” (referring to genes and proteins) with “Timing Fidelity” (referring to the accuracy of the cycle). It provides a quantitative, high-resolution measure of internal clock health, moving beyond simple behavioral observations. The concept is central to understanding the cellular basis of circadian function.
Mechanism
Fidelity is maintained by a complex transcriptional-translational feedback loop involving the CLOCK and BMAL1 genes driving the expression of Period (PER) and Cryptochrome (CRY) genes. PER and CRY proteins then feedback to inhibit CLOCK/BMAL1 activity, completing the cycle over approximately 24 hours. The precise phosphorylation and degradation rates of the PER and CRY proteins are crucial for ensuring the accurate duration and amplitude of this molecular oscillation.
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