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Cryptochrome

NiNU L, AHMAD M, MiARELLi c, CASHMORE A R and GiULiANO G (1999) Cryptochrome 1 controls tomato development in response to blue light , Plant J, 18, 551-6. [Pg.278]

Folate and FAD are also components of cryptochromes, proteins widespread in living organisms. Cryptochromes are considered photolyase sequence homologues with no DNA repair activities but with blue light-activated factors. Cryptochromes regulate growth and development in plants and seem to be responsible for the synchronization of circadian rhythms in animals and human. ... [Pg.113]

Sancar, A., Structure and function of DNA photolyase and cryptochrome blue-light... [Pg.121]

Sancar, A., Regulation of the mammalian circadian clock by cryptochrome, J. Biol. Chem., 279, 34079, 2004. [Pg.121]

Partch, C. L. et al., Postranslational regulation of mammalian circadian clock by cryptochrome and proteinphosphatase 5, Proc Aarf Acad. Sci. USA, 103, 10467, 2006. Briggs, W.R., Christie, J.M., and Salomon, M., Phototropins a new family of flavinbinding blue light receptors in plants, Antioxid. Redox Signal, 3, 775, 2001. Briggs,W.R. et al.. The phototropin family of photoreceptors. Plant Cell, 13, 993, 2001. [Pg.121]

WADE, H.K., BIBIKOVA, T.N., VALENTINE, W.J., JENKINS, G.I., Interactions within a network of phytochrome, cryptochrome and UV-B phototransduction pathways regulate chalcone synthase gene expression in Arabidopsis leaf tissue, Plant J., 2001, 25, 675-685. [Pg.108]

Ahmad M, Grancher N, Heil M et al 2002 Action spectrum for cryptochrome-dependent hypocotyl growth inhibition in A-rabidopsis. Plant Physiol 129 774—785 Baldwin JM, Schertler GF, Unger VM 1997 An alpha-carbon template for the transmembrane helices in the rhodopsin family of G-protein-coupled receptors. J Mol Biol 272 144—164 Batni S, Scalzetti L, Moody S A, Knox BE 1996 Characterization of the Xenopus rhodopsin gene. J Biol Chem 271 3179-3186... [Pg.21]

Bridges C 1959 The visual pigments of some common laboratory animals. Nature 184 727-728 Burns ME, Baylor DA 2001 Activation, deactivation, and adaptation in vertebrate photoreceptor cells. Annu Rev Neurosci 24 779-805 Cashmore AR, Jarillo JA, Wu Y-J, Liu D 1999 Cryptochromes blue light receptors for plants and animals. Science 284 760-765... [Pg.21]

Rollag MD, Provencio I, Sugden D, Green CB 2000 Cultured amphibian melanophores a model system to study melanopsin photobiology. Methods Enzymol 316 291—309 Sancar A 2000 Cryptochrome the second photoactive pigment in the eye and its role in circadian photoreception. Annu Rev Biochem 69 31—67... [Pg.23]

Young It is not so much a question of what the opsins are doing, but that of the nature of cr3rptochrome, which is a promiscuous protein. When do you expect to find cryptochrome by itself, as opposed to stuck with a dozen or so partners What would you imagine that those partnerships might do to assays of this sort Presumably these in vitro assays that have been done in A rabidopsis and algae have been quite distinct from the in vivo situation. [Pg.25]

Kay Cryptochromes are particularly problematic in matching action spectra to absorption spectra. [Pg.25]

Kay That was a good experiment that Margaret Ahmad did. She over-expressed cryptochrome and then used levels of light that are much lower and which don t initiate a response in the wild-type but do in the over-expressor. This is how she was able to determine a CRYl-specific action spectrum. [Pg.25]

Foster Tony Cashmore has consistently argued that we simply can t know what the absorption spectra of the cryptochromes will be. Others have argued differently. The empirical evidence of a comparison between a flavin absorption spectrum and that of the new CRYl over-expression by Ahmad and colleagues suggests that there is a close correlation. [Pg.25]

Cryptochromes and inner retinal non-visual irradiance detection... [Pg.31]

Generation of retinol-binding protein knockout (Quadro et al 1999), cryptochrome knockout (Thresher et al 1998, Vitaterna et al 1999), and... [Pg.32]

Ketinal-degenerate mice lacking cryptochromes show markedly decreasedphotic sensitivity for behaviour and photic induction of SCNgene expression... [Pg.34]

The decreased behavioural photoresponsiveness in cryptochrome-mutant mice is somewhat difficult to interpret since these mice also lack free-running circadian rhythms. Therefore, one is measuring masking, not circadian responses. Although masking is also preserved in retinal-degenerate animals (Mrosovsky et al 2000), the neural and molecular mechanisms of masking are not as well understood as those of circadian rhythms. [Pg.35]

Retinal-degenerate mice lacking cryptochromes show markedly decreased behavioural photoresponses and pupillary responses, while non-degenerate mice lacking cryptochromes show intact photic signalling... [Pg.36]

Mice lacking cryptochromes and ocular retinal show no photic induction of immediate early genes in the SCN... [Pg.36]

It is theoretically possible that cryptochromes do not function as photopigments, but are required either for the production of another photopigment, or for the signal transduction pathway of another photopigment. Such a pigment would need to be fully resistant to severe vitamin A depletion (since photic immediate-early gene induction in the SCN is fully preserved in RBP I mice but lost in mice) and so is unlikely to be opsin-... [Pg.39]


See other pages where Cryptochrome is mentioned: [Pg.368]    [Pg.265]    [Pg.437]    [Pg.449]    [Pg.101]    [Pg.20]    [Pg.31]    [Pg.32]    [Pg.32]    [Pg.33]    [Pg.33]    [Pg.34]    [Pg.34]    [Pg.34]    [Pg.34]    [Pg.35]    [Pg.35]    [Pg.36]    [Pg.37]    [Pg.37]    [Pg.38]    [Pg.38]    [Pg.39]    [Pg.39]    [Pg.39]    [Pg.40]    [Pg.40]    [Pg.40]   
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See also in sourсe #XX -- [ Pg.89 ]

See also in sourсe #XX -- [ Pg.41 ]

See also in sourсe #XX -- [ Pg.105 ]




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