Author:
Goda Tadahiro,Doi Masao,Umezaki Yujiro,Murai Iori,Shimatani Hiroyuki,Chu Michelle L.,Nguyen Victoria H.,Okamura Hitoshi,Hamada Fumika N.
Abstract
Daily body temperature rhythm (BTR) is essential for maintaining homeostasis. BTR is regulated separately from locomotor activity rhythms, but its molecular basis is largely unknown. While mammals internally regulate BTR, ectotherms, including Drosophila, exhibit temperature preference rhythm (TPR) behavior to regulate BTR. Here, we demonstrate that the diuretic hormone 31 receptor (DH31R) mediates TPR during the active phase in Drosophila. DH31R is expressed in clock cells, and its ligand, DH31, acts on clock cells to regulate TPR during the active phase. Surprisingly, the mouse homolog of DH31R, calcitonin receptor (Calcr), is expressed in the suprachiasmatic nucleus (SCN) and mediates body temperature fluctuations during the active phase in mice. Importantly, DH31R and Calcr are not required for coordinating locomotor activity rhythms. Our results represent the first molecular evidence that BTR is regulated distinctly from locomotor activity rhythms and show that DH31R/Calcr is an ancient specific mediator of BTR during the active phase in organisms ranging from ectotherms to endotherms.
Funder
Trustee
Cincinnati Children's Hospital
Japan Science and Technology
Precursory Research for Embryonic Science and Technology
March of Dimes
National Institutes of Health
JST/Core Research for Evolutional Science and Technology
Project for Elucidating and Controlling Mechanisms of Aging and Longevity
Japan Agency for Medical Research and Development
Ministry of Education, Culture, Sports, Science, and Technology of Japan
Publisher
Cold Spring Harbor Laboratory
Subject
Developmental Biology,Genetics
Cited by
42 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献