This proposal addresses the molecular control of biological clocks in individual organisms and single cells. Higher plants comprise one system for these studies, in part because these organisms provide cis-acting DNA elements that mediate clock-controlled gene expression. To exploit this property, a non-invasive assay has been developed for clock-regulated gene expression in intact whole plants: the promoter of a clock-regulated gene (cab2) from Arabidopsis has been fused to a cDNA encoding firefly luciferase and transgenic plants were generated containing this construct. Preliminary data demonstrate that when plants transformed by the cab2- luciferase gene fusion are sprayed with luciferin, the plants f""""""""glow"""""""" rhythmically, indicating that circadian-regulated transcription can be monitored in intact tissue. We propose to extend this technology to the analysis of dock-regulated transcription in single plant cells. The hypothesis is that individual cells of metazoan organisms can contain circadian clocks. The plant system will provide a powerful cell-level assay to address this issue. We will also identify biochemically the signal transduction pathways between the oscillator and the cab gene promoter in a plant suspension cell culture, to test the hypothesis that calmodulin-dependent pathways are important in regulating cab gene transcription. In another system, Drosophila, cis-acting elements of a 'clock locus' called period have been shown to be involved in mediating cyclic variations in per gene product levels. It is proposed to apply the luciferase reporter system to analysis of the molecular rhythm at the whole-fly level. The specific experiments will involve per-luciferase fusions and transgenic strains analogous to those in Arabidopsis. If individual flies can be shown to glow rhythmically, this will permit several important questions to be asked: Are per-related molecular cyclings actually correlated with behavioral circadian rhythms of Drosophila? The latter are controlled (in part) by per's action, and the flies rest/activity cycles persist for many days in constant conditions: so how long does the molecular rhythm persist? Can light-induced phase shifts of Drosophila's biological rhythmicity be shown to correlate with phase alterations of per-controlled protein cyclings? It is further suggested that the per-luciferase fusion system could eventually be applied to experiments aimed at asking at the molecular level if individual animal cells contain circadian clocks and if these pacemakers share common properties with those of plants? Given the ubiquity of circadian-regulated physiology, the identification of common clock components will have an impact on understanding the pacemaker mechanism and malfunctions associated with known features of human well-being.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
1R01MH051573-01A1
Application #
2250846
Study Section
Molecular, Cellular, and Developmental Neurobiology Review Committee (MCDN)
Project Start
1994-09-30
Project End
1997-08-31
Budget Start
1994-09-30
Budget End
1995-08-31
Support Year
1
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Virginia
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001910777
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Ramanathan, Chidambaram; Xu, Haiyan; Khan, Sanjoy K et al. (2014) Cell type-specific functions of period genes revealed by novel adipocyte and hepatocyte circadian clock models. PLoS Genet 10:e1004244
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
Evans, Jennifer A; Pan, Haiyun; Liu, Andrew C et al. (2012) Cry1-/- circadian rhythmicity depends on SCN intercellular coupling. J Biol Rhythms 27:443-52
Lee, Jae Wook; Hirota, Tsuyoshi; Peters, Eric C et al. (2011) A small molecule modulates circadian rhythms through phosphorylation of the period protein. Angew Chem Int Ed Engl 50:10608-11
Atwood, Ann; DeConde, Robert; Wang, Susanna S et al. (2011) Cell-autonomous circadian clock of hepatocytes drives rhythms in transcription and polyamine synthesis. Proc Natl Acad Sci U S A 108:18560-5
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
Welsh, David K; Takahashi, Joseph S; Kay, Steve A (2010) Suprachiasmatic nucleus: cell autonomy and network properties. Annu Rev Physiol 72:551-77

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