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Shell neurons of the master circadian clock coordinate the phase of tissue clocks throughout the brain and body

Overview of attention for article published in BMC Biology, June 2015
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Title
Shell neurons of the master circadian clock coordinate the phase of tissue clocks throughout the brain and body
Published in
BMC Biology, June 2015
DOI 10.1186/s12915-015-0157-x
Pubmed ID
Authors

Jennifer A. Evans, Ting-Chung Suen, Ben L. Callif, Andrew S. Mitchell, Oscar Castanon-Cervantes, Kimberly M. Baker, Ian Kloehn, Kenkichi Baba, Brett J. W. Teubner, J. Christopher Ehlen, Ketema N. Paul, Timothy J. Bartness, Gianluca Tosini, Tanya Leise, Alec J. Davidson

Abstract

Daily rhythms in mammals are programmed by a master clock in the suprachiasmatic nucleus (SCN). The SCN contains two main compartments (i.e., shell and core), but the role of each region in system-level coordination remains ill defined. Here we use a functional assay to investigate how downstream tissues interpret region-specific outputs by using in vivo exposure to long day photoperiods to temporally dissociate the SCN. We then analyze resulting changes in the rhythms of clocks located throughout the brain and body to examine whether they maintain phase synchrony with the SCN shell or core. Nearly all of the 17 tissues examined in the brain and body maintain phase synchrony with the SCN shell, but not the SCN core, which indicates that downstream oscillators are set by cues controlled specifically by the SCN shell. Interestingly, we also found that SCN dissociation diminished the amplitude of rhythms in core clock gene and protein expression in brain tissues by 50-75 %, which suggests that light-driven changes in the functional organization of the SCN markedly influence the strength of rhythms in downstream tissues. Overall, our results reveal that body clocks receive time-of-day cues specifically from the SCN shell, which may be an adaptive design principle that serves to maintain system-level phase relationships in a changing environment. Further, we demonstrate that lighting conditions alter the amplitude of the molecular clock in downstream tissues, which uncovers a new form of plasticity that may contribute to seasonal changes in physiology and behavior.

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Mendeley readers

The data shown below were compiled from readership statistics for 101 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 4 4%
United States 1 <1%
Unknown 96 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 26 26%
Researcher 14 14%
Student > Bachelor 11 11%
Student > Postgraduate 7 7%
Student > Doctoral Student 6 6%
Other 16 16%
Unknown 21 21%
Readers by discipline Count As %
Agricultural and Biological Sciences 24 24%
Neuroscience 23 23%
Biochemistry, Genetics and Molecular Biology 8 8%
Medicine and Dentistry 7 7%
Pharmacology, Toxicology and Pharmaceutical Science 3 3%
Other 13 13%
Unknown 23 23%