SCFFbxl3 controls the oscillation of the circadian clock by directing the degradation of cryptochrome proteins

被引:449
作者
Busino, Luca
Bassermann, Florian
Maiolica, Alessio
Lee, Choogon
Nolan, Patrick M.
Godinho, Sofia I. H.
Draetta, Giulio F.
Pagano, Michele
机构
[1] NYU, Dept Pathol, Inst Canc, Sch Med, New York, NY 10016 USA
[2] European Inst Oncol, I-20141 Milan, Italy
[3] Florida State Univ, Dept Biomed Sci, Coll Med, Tallahassee, FL 32306 USA
[4] MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England
[5] Merck Res Labs, Boston, MA 02115 USA
基金
英国医学研究理事会;
关键词
D O I
10.1126/science.1141194
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
One component of the circadian clock in mammals is the Clock-Bmal1 heterodimeric transcription factor. Among its downstream targets, two genes, Cry1 and Cry2, encode inhibitors of the Clock-Bmal1 complex that establish a negative-feedback loop. We found that both Cry1 and Cry2 proteins are ubiquitinated and degraded via the SCFFbxl3 ubiquitin ligase complex. This regulation by SCFFbxl3 is a prerequisite for the efficient and timely reactivation of Clock-Bmal1 and the consequent expression of Per1 and Per2, two regulators of the circadian clock that display tumor suppressor activity. Silencing of Fbxl3 produced no effect in Cry1(-/-); Cry2(-/-) cells, which shows that Fbxl3 controls clock oscillations by mediating the degradation of CRY proteins.
引用
收藏
页码:900 / 904
页数:5
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