4.8 Article

Dissociation of Per1 and Bmal1 circadian rhythms in the suprachiasmatic nucleus in parallel with behavioral outputs

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1613374114

Keywords

clock gene; in vivo recording; suprachiasmatic nucleus; photic phase resetting; E and M oscillators

Funding

  1. Uehara Memorial Foundation
  2. Nakajima Foundation
  3. Project for Developing Innovation Systems of the Ministry of Education, Culture, Sports, Science and Technology (MEXT)
  4. Creation of Innovation Centers for Advanced Interdisciplinary Research Areas Program, MEXT
  5. Japan Society for the Promotion of Science [15H04679, 26860156, 15K12763]
  6. Grants-in-Aid for Scientific Research [15H04679, 15K12763, 15KT0072, 26860156, 17K08561] Funding Source: KAKEN

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The temporal order of physiology and behavior in mammals is primarily regulated by the circadian pacemaker located in the hypothalamic suprachiasmatic nucleus (SCN). Taking advantage of bioluminescence reporters, we monitored the circadian rhythms of the expression of clock genes Per1 and Bmal1 in the SCN of freely moving mice and found that the rate of phase shifts induced by a single light pulse was different in the two rhythms. The Per1-luc rhythm was phase-delayed instantaneously by the light presented at the subjective evening in parallel with the activity onset of behavioral rhythm, whereas the Bmal1-ELuc rhythm was phasedelayed gradually, similar to the activity offset. The dissociation was confirmed in cultured SCN slices of mice carrying both Per1-luc and Bmal1-ELuc reporters. The two rhythms in a single SCN slice showed significantly different periods in a long-term (3 wk) culture and were internally desynchronized. Regional specificity in the SCN was not detected for the period of Per1-luc and Bmal1-ELuc rhythms. Furthermore, neither is synchronized with circadian intracellular Ca2+ rhythms monitored by a calcium indicator, GCaMP6s, or with firing rhythms monitored on a multielectrode array dish, although the coupling between the circadian firing and Ca2+ rhythms persisted during culture. These findings indicate that the expressions of two key clock genes, Per1 and Bmal1, in the SCN are regulated in such a way that they may adopt different phases and free-running periods relative to each other and are respectively associated with the expression of activity onset and offset.

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