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dc.contributor.authorGegear, Robert J.
dc.contributor.authorFoley, Lauren E.
dc.contributor.authorCasselman, Amy L.
dc.contributor.authorReppert, Steven M.
dc.date2022-08-11T08:09:29.000
dc.date.accessioned2022-08-23T16:32:38Z
dc.date.available2022-08-23T16:32:38Z
dc.date.issued2010-02-11
dc.date.submitted2012-05-24
dc.identifier.citationNature. 2010 Feb 11;463(7282):804-7. Epub 2010 Jan 24. <a href="http://dx.doi.org/10.1038/nature08719">Link to article on publisher's site</a>
dc.identifier.issn0028-0836 (Linking)
dc.identifier.doi10.1038/nature08719
dc.identifier.pmid20098414
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37927
dc.description.abstractUnderstanding the biophysical basis of animal magnetoreception has been one of the greatest challenges in sensory biology. Recently it was discovered that the light-dependent magnetic sense of Drosophila melanogaster is mediated by the ultraviolet (UV)-A/blue light photoreceptor cryptochrome (Cry). Here we show, using a transgenic approach, that the photoreceptive, Drosophila-like type 1 Cry and the transcriptionally repressive, vertebrate-like type 2 Cry of the monarch butterfly (Danaus plexippus) can both function in the magnetoreception system of Drosophila and require UV-A/blue light (wavelength below 420 nm) to do so. The lack of magnetic responses for both Cry types at wavelengths above 420 nm does not fit the widely held view that tryptophan triad-generated radical pairs mediate the ability of Cry to sense a magnetic field. We bolster this assessment by using a mutant form of Drosophila and monarch type 1 Cry and confirm that the tryptophan triad pathway is not crucial in magnetic transduction. Together, these results suggest that animal Crys mediate light-dependent magnetoreception through an unconventional photochemical mechanism. This work emphasizes the utility of Drosophila transgenesis for elucidating the precise mechanisms of Cry-mediated magnetosensitivity in insects and also in vertebrates such as migrating birds.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20098414&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820607/pdf/nihms166367.pdf
dc.subjectAnimal Migration
dc.subjectAnimals
dc.subjectAnimals, Genetically Modified
dc.subjectButterflies
dc.subjectCryptochromes
dc.subjectDrosophila Proteins
dc.subjectDrosophila melanogaster
dc.subjectEye Proteins
dc.subject*Magnetics
dc.subjectOrientation
dc.subject*Photochemical Processes
dc.subjectPhotoreceptor Cells, Invertebrate
dc.subjectTransgenes
dc.subjectNeuroscience and Neurobiology
dc.titleAnimal cryptochromes mediate magnetoreception by an unconventional photochemical mechanism
dc.typeJournal Article
dc.source.journaltitleNature
dc.source.volume463
dc.source.issue7282
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neurobiology_pp/20
dc.identifier.contextkey2911135
html.description.abstract<p>Understanding the biophysical basis of animal magnetoreception has been one of the greatest challenges in sensory biology. Recently it was discovered that the light-dependent magnetic sense of Drosophila melanogaster is mediated by the ultraviolet (UV)-A/blue light photoreceptor cryptochrome (Cry). Here we show, using a transgenic approach, that the photoreceptive, Drosophila-like type 1 Cry and the transcriptionally repressive, vertebrate-like type 2 Cry of the monarch butterfly (Danaus plexippus) can both function in the magnetoreception system of Drosophila and require UV-A/blue light (wavelength below 420 nm) to do so. The lack of magnetic responses for both Cry types at wavelengths above 420 nm does not fit the widely held view that tryptophan triad-generated radical pairs mediate the ability of Cry to sense a magnetic field. We bolster this assessment by using a mutant form of Drosophila and monarch type 1 Cry and confirm that the tryptophan triad pathway is not crucial in magnetic transduction. Together, these results suggest that animal Crys mediate light-dependent magnetoreception through an unconventional photochemical mechanism. This work emphasizes the utility of Drosophila transgenesis for elucidating the precise mechanisms of Cry-mediated magnetosensitivity in insects and also in vertebrates such as migrating birds.</p>
dc.identifier.submissionpathneurobiology_pp/20
dc.contributor.departmentGraduate School of Biomedical Sciences, Neuroscience Program
dc.contributor.departmentReppert Lab
dc.contributor.departmentNeurobiology
dc.source.pages804-7


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