Abstract
The arabidopsis thaliana HY4 gene encodes CRY1, a 75-kilodalton flavoprotein mediating blue light-dependent regulation of seedling development. CRY1 is demonstrated here to noncovalently bind stoichiometric amounts of flavin adenine dinucleotide (FAD). The redox properties of FAD bound by CRY1 include an unexpected stability of the neutral radical flavosemiquinone (FADH.). The absorption properties of this flavosemiquinone provide a likely explanation for the additional sensitivity exhibited by CRY1-mediated responses in the green region of the visible spectrum. Despite the sequence homology to microbial DNA photolyases, CRY1 was found to have no detectable photolyase activity.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Arabidopsis / genetics
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Arabidopsis / metabolism*
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Arabidopsis Proteins
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Cryptochromes
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Deoxyribodipyrimidine Photo-Lyase / metabolism
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Drosophila Proteins*
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Eye Proteins*
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Flavoproteins / chemistry
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Flavoproteins / genetics
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Flavoproteins / metabolism*
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Genes, Plant
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Light
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Oxidation-Reduction
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Photoreceptor Cells, Invertebrate*
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Plant Proteins / chemistry
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Plant Proteins / genetics
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Plant Proteins / metabolism*
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Quinones / metabolism
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Receptors, G-Protein-Coupled
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Spectrum Analysis
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Ultraviolet Rays
Substances
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Arabidopsis Proteins
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CRY1 protein, Arabidopsis
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Cryptochromes
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Drosophila Proteins
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Eye Proteins
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Flavoproteins
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Plant Proteins
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Quinones
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Receptors, G-Protein-Coupled
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cry protein, Drosophila
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flavosemiquinone
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Deoxyribodipyrimidine Photo-Lyase