Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 104, Issue 37, Pages 14712-14717Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.0704588104
Keywords
entrainment; oscillator; phase shift; photoperiod
Categories
Funding
- Biotechnology and Biological Sciences Research Council [BBS/B/02886] Funding Source: researchfish
- Biotechnology and Biological Sciences Research Council [BBS/B/02886] Funding Source: Medline
- Wellcome Trust Funding Source: Medline
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Zebrafish tissues and cells have the unusual feature of not only containing a circadian clock, but also being directly light-responsive. Several zebraf ish genes are induced by light, but little is known about their role in clock resetting or the mechanism by which this might occur. Here we show that Cryptochrome la (Cry1a) plays a key role in light entrainment of the zebraf ish clock. intensity and phase response curves reveal a strong correlation between light induction of Cry1a and clock resetting. Overexpression studies show that Cry1a acts as a potent repressor of clock function and mimics the effect of constant light to stop the circadian oscillator. Yeast two-hybrid analysis demonstrates that the Cry1a protein interacts directly with specific regions of core clock components, CLOCK and BMAL, blocking their ability to fully dimerize and transactivate downstream targets, providing a likely mechanism for clock resetting. A comparison of entrainment of zebrafish cells to complete versus skeleton photoperiods reveals that clock phase is identical under these two conditions. However, the amplitude of the core clock oscillation is much higher on a complete photoperiod, as are the levels of light-induced Cty1a. We believe that Cry1a acts on the core clock machinery in both a continuous and discrete fashion, leading not only to entrainment, but also to the establishment of a high-amplitude rhythm and even stopping of the clock under long photoperiods.
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