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In Vivo Role of Phosphorylation of Cryptochrome 2 in the Mouse Circadian Clock
Author(s) -
Arisa Hirano,
Nobuhiro Kurabayashi,
Tomoki Nakagawa,
Go Shioi,
Takeshi Todo,
Tsuyoshi Hirota,
Yoshitaka Fukada
Publication year - 2014
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.00711-14
Subject(s) - per2 , biology , cryptochrome , circadian clock , circadian rhythm , microbiology and biotechnology , phosphorylation , mutant , period (music) , ubiquitin , in vivo , clock , genetics , neuroscience , gene , physics , acoustics
The circadian clock is finely regulated by posttranslational modifications of clock components. Mouse CRY2, a critical player in the mammalian clock, is phosphorylated at Ser557 for proteasome-mediated degradation, but itsin vivo role in circadian organization was not revealed. Here, we generated CRY2(S557A) mutant mice, in which Ser557 phosphorylation is specifically abolished. The mutation lengthened free-running periods of the behavioral rhythms and PER2::LUC bioluminescence rhythms of cultured liver. In livers from mutant mice, the nuclear CRY2 level was elevated, with enhanced PER2 nuclear occupancy and suppression of E-box-regulated genes. Thus, Ser557 phosphorylation-dependent regulation of CRY2 is essential for proper clock oscillationin vivo .

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