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Mol Cell Biol, April 1998, p. 2004-2013, Vol. 18, No. 4
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Differential Effects of Light and Heat on the
Drosophila Circadian Clock Proteins PER and TIM
David
Sidote,1
John
Majercak,2
Vaishali
Parikh,3,
and
Isaac
Edery1,*
Department of Molecular Biology and
Biochemistry1 and
Biochemistry Graduate
Program,2 Center for Advanced Biotechnology and
Medicine, Rutgers University, and
Center for Advanced
Biotechnology and Medicine, University of Medicine and Dentistry of
New Jersey,3 Piscataway, New Jersey 08854
Received 21 August 1997/Returned for modification 1 October
1997/Accepted 6 January 1998
Circadian (
24-h) rhythms are governed by endogenous biochemical
oscillators (clocks) that in a wide variety of organisms can be phase
shifted (i.e., delayed or advanced) by brief exposure to light and
changes in temperature. However, how changes in temperature reset
circadian timekeeping mechanisms is not known. To begin to address this
issue, we measured the effects of short-duration heat pulses on the
protein and mRNA products from the Drosophila circadian
clock genes period (per) and
timeless (tim). Heat pulses at all times in a
daily cycle elicited dramatic and rapid decreases in the levels of PER
and TIM proteins. PER is sensitive to heat but not light, indicating
that individual clock components can markedly differ in sensitivity to
environmental stimuli. A similar resetting mechanism involving delays
in the per-tim transcriptional-translational feedback loop
likely underlies the observation that when heat and light signals are
administered in the early night, they both evoke phase delays in
behavioral rhythms. However, whereas previous studies showed that the
light-induced degradation of TIM in the late night is accompanied by
stable phase advances in the temporal regulation of the PER and TIM
biochemical rhythms, the heat-induced degradation of PER and TIM at
these times in a daily cycle results in little, if any, long-term
perturbation in the cycles of these clock proteins. Rather, the initial
heat-induced degradation of PER and TIM in the late night is followed
by a transient and rapid increase in the speed of the PER-TIM temporal
program. The net effect of these heat-induced changes results in an
oscillatory mechanism with a steady-state phase similar to that of the
unperturbed control situation. These findings can account for the lack
of apparent steady-state shifts in Drosophila behavioral
rhythms by heat pulses applied in the late night and strongly suggest that stimulus-induced changes in the speed of circadian clocks can
contribute to phase-shifting responses.
*
Corresponding author. Mailing address: Department of
Molecular Biology and Biochemistry, CABM, 679 Hoes Lane, Piscataway, NJ
08854. Phone: (732) 235-5550. Fax: (732) 235-5318. E-mail: edery{at}mbcl.rutgers.edu.

Present address: Department of Molecular Biology and Genetics,
Johns Hopkins University School of Medicine, Baltimore, MD
21205.
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