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    Redox potential: differential roles in dCRY and mCRY1 functions

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    Authors
    Froy, Oren
    Chang, Dennis C.
    Reppert, Steven M.
    UMass Chan Affiliations
    Reppert Lab
    Neurobiology
    Document Type
    Journal Article
    Publication Date
    2002-01-22
    Keywords
    Neuroscience and Neurobiology
    
    Metadata
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    Link to Full Text
    http://dx.doi.org/10.1016/S0960-9822(01)00656-X
    Abstract
    Cryptochromes (CRYs) are flavoproteins important for the molecular clocks of animals. The Drosophila cryptochrome (dCRY) is a circadian photoreceptor, whereas mouse cryptochromes (mCRY1 and mCRY2) are essential negative elements of circadian clock transcriptional feedback loops. It has been proposed that reduction/oxidation (redox) reactions are important for dCRY light responsiveness and mCRY1 transcriptional inhibition. We therefore evaluated the role of redox in light-dependent activation of dCRY and in mCRY1 transcriptional inhibition in Drosophila Schneider 2 cells. Using site-directed mutagenesis, three of the four conserved flavin binding residues in dCRY were found to be essential for light responses, whereas three of the four corresponding residues in mCRY1 did not abolish transcriptional responses. Two tryptophan residues in dCRY are critical for its function and are likely involved in an intramolecular redox reaction. The corresponding tryptophan residues do not play a redox-mediated role in mCRY1 function. The data provide a multistep redox model for the light-dependent activities of dCRY and suggest that such a model does not apply to mCRY1 transcriptional responses.
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/48655
    PubMed ID
    11818067
    Notes

    Dennis Chang is a PhD student in the Reppert Lab at UMass Medical School.

    Related Resources
    Link to article in PubMed
    Rights
    Citation: Froy O, Chang DC, Reppert SM. Redox potential: differential roles in dCRY and mCRY1 functions. Curr Biol. 2002 Jan 22;12(2):147-52. PubMed PMID: 11818067.
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