This proposal investigates the molecular mechanisms that regulate biological clocks, from the perception of environmental inputs and cellular signals to the initiation of downstream gene expression changes. Biological clocks function in the coordination of gene expression, physiological, and behavioral events at critical times of the day, contributing to adaptive advantages by allowing for the anticipation of daily environmental changes. Substantial progress in the investigation of biological clocks has identified a transcriptional feedback loop, a mechanism conserved throughout numerous organisms. However, less is known about how external stimuli, such as light, are transmitted to the clock, as well as what signal transduction pathways are responsible for transmitting these stimuli. Furthermore, little is known about the functions of the genes whose expression is controlled by the clock. In Drosophila, we have shown that dCLOCK and dCYCLE activate transcription together by binding to E-boxes in the promoters of period and timeless in in vitro expression assays. With this in vitro assay, we have also identified the PER/TIM complex as a potent inhibitor of dCLK/dCYC and determined that the photoreceptor, cryptochrome (CRY), can both bind to TIM and relieve PER/TIM inhibition in light-dependent manners. We have also implicated CBP/p300, a component of the CREB-signaling pathway, in regulating the activity of dCLK/dCYC. Finally, we have used high density oligonucleotide arrays to identify circadianly-expressed genes under clock control. In addition, we propose to investigate the molecular functions of two clock-controlled genes identified in our genome-wide analysis. Our analysis will provide substantial insight into the molecular regulation of circadian clocks and novel information on the links between phototransduction and the regulation of gene expression. Furthermore, because many of these components, pathways, and mechanisms are conserved, our investigation will have significant impact on the understanding of biological clocks and the human diseases that occur from circadian dysfunction.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH051573-12
Application #
6894806
Study Section
Special Emphasis Panel (ZRG1-IFCN-3 (01))
Program Officer
Beckel-Mitchener, Andrea C
Project Start
1994-09-30
Project End
2007-05-31
Budget Start
2005-06-01
Budget End
2006-05-31
Support Year
12
Fiscal Year
2005
Total Cost
$469,250
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
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St John, Peter C; Hirota, Tsuyoshi; Kay, Steve A et al. (2014) Spatiotemporal separation of PER and CRY posttranslational regulation in the mammalian circadian clock. Proc Natl Acad Sci U S A 111:2040-5
Hirota, Tsuyoshi; Lee, Jae Wook; St John, Peter C et al. (2012) Identification of small molecule activators of cryptochrome. Science 337:1094-7
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Zhang, Eric E; Liu, Yi; Dentin, Renaud et al. (2010) Cryptochrome mediates circadian regulation of cAMP signaling and hepatic gluconeogenesis. Nat Med 16:1152-6
Hirota, Tsuyoshi; Lee, Jae Wook; Lewis, Warren G et al. (2010) High-throughput chemical screen identifies a novel potent modulator of cellular circadian rhythms and reveals CKI? as a clock regulatory kinase. PLoS Biol 8:e1000559
Ko, Caroline H; Yamada, Yujiro R; Welsh, David K et al. (2010) Emergence of noise-induced oscillations in the central circadian pacemaker. PLoS Biol 8:e1000513
Zhang, Eric E; Kay, Steve A (2010) Clocks not winding down: unravelling circadian networks. Nat Rev Mol Cell Biol 11:764-76

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