Author
Listed:
- Shailesh Kumar
(University of Pennsylvania)
- Dechun Chen
(University of Pennsylvania)
- Christopher Jang
(University of Pennsylvania)
- Alexandra Nall
(University of Pennsylvania)
- Xiangzhong Zheng
(University of Pennsylvania)
- Amita Sehgal
(University of Pennsylvania
Howard Hughes Medical Institute, Perelman School of Medicine, University of Pennsylvania)
Abstract
Little is known about molecular links between circadian clocks and steroid hormone signalling, although both are important for normal physiology. Here we report a circadian function for a nuclear receptor, ecdysone-induced protein 75 (Eip75/E75), which we identified through a gain-of-function screen for circadian genes in Drosophila melanogaster. Overexpression or knockdown of E75 in clock neurons disrupts rest:activity rhythms and dampens molecular oscillations. E75 represses expression of the gene encoding the transcriptional activator, CLOCK (CLK), and may also affect circadian output. PER inhibits the activity of E75 on the Clk promoter, thereby providing a mechanism for a previously proposed de-repressor effect of PER on Clk transcription. The ecdysone receptor is also expressed in central clock cells and manipulations of its expression produce effects similar to those of E75 on circadian rhythms. We find that E75 protects rhythms under stressful conditions, suggesting a function for steroid signalling in the maintenance of circadian rhythms in Drosophila.
Suggested Citation
Shailesh Kumar & Dechun Chen & Christopher Jang & Alexandra Nall & Xiangzhong Zheng & Amita Sehgal, 2014.
"An ecdysone-responsive nuclear receptor regulates circadian rhythms in Drosophila,"
Nature Communications, Nature, vol. 5(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6697
DOI: 10.1038/ncomms6697
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