Circadian physiology is regulated by a cell-autonomous transcriptional negative feedback loop that influences multiple aspects of behavior. Disturbances in circadian rhythm underlie problems such as industrial and automobile accidents and sleep disorders. A detailed understanding of the function of the clock may aid in the mitigation of these problems. The genes and proteins that make up the machinery of the mammalian circadian rhythms are being identified through genetic approaches. The molecular mechanisms that underlie the intrinsic 24-hour clock can now be analyzed through the study of these regulatory elements in vivo and in vitro. Mutations in casein kinase I epsilon (CKIepsilon) both in flies and hamsters have recently been found to significantly dysregulate clock function, demonstrating that protein phosphorylation by a specific protein kinase plays a critical in the regulation of the clock. Initial mechanistic studies have suggested that CKIepsilon binds to the PERIOD proteins and through phosphorylation regulates their stability and nucleocytoplasmic trafficking. This project will examine specific mechanisms by which phosphorylation regulates the function of the circadian clock by a combination of molecular and genetic approaches.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM060387-04
Application #
6835143
Study Section
Visual Sciences C Study Section (VISC)
Program Officer
Tompkins, Laurie
Project Start
2002-01-01
Project End
2006-12-31
Budget Start
2005-01-01
Budget End
2006-12-31
Support Year
4
Fiscal Year
2005
Total Cost
$299,000
Indirect Cost
Name
University of Utah
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
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Stoltzman, Carrie A; Kaadige, Mohan R; Peterson, Christopher W et al. (2011) MondoA senses non-glucose sugars: regulation of thioredoxin-interacting protein (TXNIP) and the hexose transport curb. J Biol Chem 286:38027-34
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Yamada, Yr; Forger, Db (2010) Multiscale complexity in the mammalian circadian clock. Curr Opin Genet Dev 20:626-33
Peterson, Christopher W; Stoltzman, Carrie A; Sighinolfi, Michael P et al. (2010) Glucose controls nuclear accumulation, promoter binding, and transcriptional activity of the MondoA-Mlx heterodimer. Mol Cell Biol 30:2887-95
Kaadige, Mohan R; Looper, Ryan E; Kamalanaadhan, Sadhaasivam et al. (2009) Glutamine-dependent anapleurosis dictates glucose uptake and cell growth by regulating MondoA transcriptional activity. Proc Natl Acad Sci U S A 106:14878-83
Stoltzman, Carrie A; Peterson, Christopher W; Breen, Kevin T et al. (2008) Glucose sensing by MondoA:Mlx complexes: a role for hexokinases and direct regulation of thioredoxin-interacting protein expression. Proc Natl Acad Sci U S A 105:6912-7
Virshup, D M; Eide, E J; Forger, D B et al. (2007) Reversible protein phosphorylation regulates circadian rhythms. Cold Spring Harb Symp Quant Biol 72:413-20

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