Drosophila TRPA1 functions in temperature control of circadian rhythm in pacemaker neurons

TitleDrosophila TRPA1 functions in temperature control of circadian rhythm in pacemaker neurons
Publication TypeJournal Article
Year of Publication2013
AuthorsLee Y, Montell C
JournalJ Neurosci
Volume33
Pagination6716-25
Date Published2013 Apr 17
ISSN1529-2401
KeywordsAnimals, Animals, Genetically Modified, Body Temperature, Brain, Chi-Square Distribution, Circadian Rhythm, Drosophila, Drosophila Proteins, Fourier Analysis, Gene Expression Regulation, Green Fluorescent Proteins, Motor Activity, Neurons, Temperature, Transcription Factors, TRPC Cation Channels
Abstract

Most animals from flies to humans count on circadian clocks to synchronize their physiology and behaviors. Daily light cycles are well known environmental cues for setting circadian rhythms. Warmer and cooler temperatures that mimic day and night are also effective in entraining circadian activity in most animals. Even vertebrate organisms can be induced to show circadian responses through exposure to temperature cycles. In poikilothermic animals such as Drosophila, temperature differences of only 2-3°C are sufficient to synchronize locomotor rhythms. However, the molecular sensors that participate in temperature regulation of circadian activity in fruit flies or other animals are enigmatic. It is also unclear whether such detectors are limited to the periphery or may be in the central brain. Here, we showed that Drosophila TRPA1 (transient receptor potential cation channel A1) was necessary for normal activity patterns during temperature cycles. The trpA1 gene was expressed in a subset of pacemaker neurons in the central brain. In response to temperature entrainment, loss of trpA1 impaired activity, and altered expression of the circadian clock protein period (Per) in a subset of pacemaker neurons. These findings underscore a role for a thermoTRP in temperature regulation that extends beyond avoidance of noxious or suboptimal temperatures.

DOI10.1523/JNEUROSCI.4237-12.2013
Alternate JournalJ. Neurosci.
PubMed ID23595730
PubMed Central IDPMC3664735
Grant ListGM085335 / GM / NIGMS NIH HHS / United States
R01 GM085335 / GM / NIGMS NIH HHS / United States