Localizing the self in time is fundamental for daily life functioning and is lacking in severe disabling neuropsychiatric disorders like schizophrenia. Brains keep track of time across an impressive range of scales. Great progress has been made in identifying the molecular machinery of the circadian clock, the brain's master clock that operates on the 24-hour scale and allows animals to know the "time of the day" that important events occur, without referring to external cues. However, the biology of interval timing, the mechanism responsible for durations in the seconds-to-minutes-to-hours range, remains a mystery, and an obvious question is whether there is a common biological solution for keeping track of time across these 2 time scales. To address this, we trained Cry1/Cry2 double knockout mice on an interval timing task with durations that ranged between 3 and 27 seconds. The mice were kept under constant light conditions to avoid any exogenously induced form of daily rhythmicity. We observed that the homozygous knockouts displayed as accurate and precise a temporal memory as the control mice. This suggests that the Cry1 and Cry2 genes are not an important component of the interval timer. Furthermore, proper calibration of the interval timer does not depend on a functional circadian clock. Thus, these 2 timing systems likely rely on different and independent biological mechanisms.

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Keywords Cry1, Cry2, circadian rhythmicity, circadian timing, cryptochromes, interval timing, mutant mice, scalar variability
Persistent URL dx.doi.org/10.1177/0748730411410026, hdl.handle.net/1765/31338
Grant This work was funded by the European Commission 7th Framework Programme; grant id fp7/208116 - A Genetics Approach to the Interval Timing Mechanism (GENETICS OF TIMING)
Papachristos, E.B, Jacobs, E.H, & Elgersma, Y. (2011). Interval timing is intact in arrhythmic cry1/Cry2-deficient mice. Journal of Biological Rhythms, 26(4), 305–313. doi:10.1177/0748730411410026