4.2 Article

Molecular and Neural Mechanisms of Temperature Preference Rhythm in Drosophila melanogaster

期刊

JOURNAL OF BIOLOGICAL RHYTHMS
卷 38, 期 4, 页码 326-340

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/07487304231171624

关键词

circadian rhythms; circadian clock; body temperature rhythm; temperature preference rhythm; dorsal neurons; diuretic hormone 31; calcitonin receptor; Drosophila melanogaster

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Temperature influences animal physiology and behavior. Mammals set their body temperatures using metabolic and behavioral strategies, while small ectotherms such as Drosophila control their body temperatures by choosing appropriate environmental temperatures. The body temperature rhythm (BTR) and temperature preference rhythm (TPR) play important roles in regulating the daily fluctuation of body temperature. The regulatory mechanisms of TPR have been summarized, including the involvement of neuropeptides and their receptors. Understanding the mechanisms of TPR in Drosophila could provide insights into the regulation of mammalian BTR and the relationship between BTR and sleep regulation.
Temperature influences animal physiology and behavior. Animals must set an appropriate body temperature to maintain homeostasis and maximize survival. Mammals set their body temperatures using metabolic and behavioral strategies. The daily fluctuation in body temperature is called the body temperature rhythm (BTR). For example, human body temperature increases during wakefulness and decreases during sleep. BTR is controlled by the circadian clock, is closely linked with metabolism and sleep, and entrains peripheral clocks located in the liver and lungs. However, the underlying mechanisms of BTR are largely unclear. In contrast to mammals, small ectotherms, such as Drosophila, control their body temperatures by choosing appropriate environmental temperatures. The preferred temperature of Drosophila increases during the day and decreases at night; this pattern is referred to as the temperature preference rhythm (TPR). As flies are small ectotherms, their body temperature is close to that of the surrounding environment. Thus, Drosophila TPR produces BTR, which exhibits a pattern similar to that of human BTR. In this review, we summarize the regulatory mechanisms of TPR, including recent studies that describe neuronal circuits relaying ambient temperature information to dorsal neurons (DNs). The neuropeptide diuretic hormone 31 (DH31) and its receptor (DH31R) regulate TPR, and a mammalian homolog of DH31R, the calcitonin receptor (CALCR), also plays an important role in mouse BTR regulation. In addition, both fly TPR and mammalian BTR are separately regulated from another clock output, locomotor activity rhythms. These findings suggest that the fundamental mechanisms of BTR regulation may be conserved between mammals and flies. Furthermore, we discuss the relationships between TPR and other physiological functions, such as sleep. The dissection of the regulatory mechanisms of Drosophila TPR could facilitate an understanding of mammalian BTR and the interaction between BTR and sleep regulation.

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