Organisms from bacteria to humans use a circadian clock to control daily biochemical, physiological, and behavioral rhythms. This clock affects human physiology, and disruptions of normal clock function can cause mental health problems, including manic depression. From studies of Neurospora and Drosophila we are beginning to understand the molecular mechanism of the clock. However, the way in which the clock regulates gene expression is largely unknown. We have identified four classes of Neurospora clock-controlled genes whose mRNA levels peak at dawn, noon, dusk and midnight. The clock in humans also regulates genes whose expression peaks at different times. Thus, a critical question is how the clock signals genes to be expressed at different times of day. One hypothesis is that a single output pathway from the clock incorporates time delays to trigger sequential expression of the different gene sets. A second hypothesis is that there are time-of-day-specific output pathways from the clock, with each pathway regulating one of the gene classes. We have developed a genetic selection to identify output-pathway genes and have found four genes (cop-1, cop-2, cop-3 and nrc-2 (cop-5)) required for rhythmicity of one or more clock-controlled genes. To test the two hypotheses, we will clone the four genes and determine how the clock affects expression, localization and/or modification of their mRNA and protein products. To map the output pathways, we will determine how mutations in any one of the four genes affects the expression of the different classes of clock-regulated genes, and the expression level, localization and/or modification of the other cop genes and COP proteins. Using biochemical and genetic methods, we will determine if known clock components interact with the COP proteins to signal time-of-day information to downstream genes. Our studies will have a significant impact on understanding how circadian clocks control overt rhythmicity and will potentially provide novel approaches for therapies for human diseases that result from circadian dysfunction.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM058529-06
Application #
6821408
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Tompkins, Laurie
Project Start
1999-08-01
Project End
2008-07-31
Budget Start
2004-08-01
Budget End
2005-07-31
Support Year
6
Fiscal Year
2004
Total Cost
$294,407
Indirect Cost
Name
Texas A&M University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
078592789
City
College Station
State
TX
Country
United States
Zip Code
77845
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Goldsmith, Charles S; Kim, Sam Moon; Karunarathna, Nirmala et al. (2018) Inhibition of p38 MAPK activity leads to cell type-specific effects on the molecular circadian clock and time-dependent reduction of glioma cell invasiveness. BMC Cancer 18:43
Caster, Stephen Z; Castillo, Kathrina; Sachs, Matthew S et al. (2016) Circadian clock regulation of mRNA translation through eukaryotic elongation factor eEF-2. Proc Natl Acad Sci U S A 113:9605-10
Hurley, Jennifer M; Dasgupta, Arko; Emerson, Jillian M et al. (2014) Analysis of clock-regulated genes in Neurospora reveals widespread posttranscriptional control of metabolic potential. Proc Natl Acad Sci U S A 111:16995-7002
Wu, Cheng; Yang, Fei; Smith, Kristina M et al. (2014) Genome-wide characterization of light-regulated genes in Neurospora crassa. G3 (Bethesda) 4:1731-45
Goldsmith, Charles S; Bell-Pedersen, Deborah (2013) Diverse roles for MAPK signaling in circadian clocks. Adv Genet 84:1-39
Bennett, Lindsay D; Beremand, Phillip; Thomas, Terry L et al. (2013) Circadian activation of the mitogen-activated protein kinase MAK-1 facilitates rhythms in clock-controlled genes in Neurospora crassa. Eukaryot Cell 12:59-69
Lamb, Teresa M; Vickery, Justin; Bell-Pedersen, Deborah (2013) Regulation of gene expression in Neurospora crassa with a copper responsive promoter. G3 (Bethesda) 3:2273-80
Lamb, Teresa M; Finch, Katelyn E; Bell-Pedersen, Deborah (2012) The Neurospora crassa OS MAPK pathway-activated transcription factor ASL-1 contributes to circadian rhythms in pathway responsive clock-controlled genes. Fungal Genet Biol 49:180-8
Lamb, Teresa M; Goldsmith, Charles S; Bennett, Lindsay et al. (2011) Direct transcriptional control of a p38 MAPK pathway by the circadian clock in Neurospora crassa. PLoS One 6:e27149

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