4.8 Article

miR-132/212 Modulates Seasonal Adaptation and Dendritic Morphology of the Central Circadian Clock

Journal

CELL REPORTS
Volume 19, Issue 3, Pages 505-520

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2017.03.057

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Funding

  1. Canadian Institute of Health Research (CIHR) [86549, 126090]
  2. Natural Sciences and Engineering Research Council (NSERC) of Canada [RGPIN386495-11]
  3. NIMH NIH HHS [MH094416]
  4. Consejo Nacional de Ciencia y Tecnologia (CONACyT) of Mexico
  5. NSERC Canada Graduate Scholarships

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The central circadian pacemaker, the suprachiasmatic nucleus (SCN), encodes day length information by mechanisms that are not well understood. Here, we report that genetic ablation of miR-132/212 alters entrainment to different day lengths and non-24 hr day-night cycles, as well as photoperiodic regulation of Period2 expression in the SCN. SCN neurons from miR-132/212-deficient mice have significantly reduced dendritic spine density, along with altered methyl CpG-binding protein (MeCP2) rhythms. In Syrian hamsters, a model seasonal rodent, day length regulates spine density on SCN neurons in a melatonin-independent manner, as well as expression of miR-132, miR-212, and their direct target, MeCP2. Genetic disruption of Mecp2 fully restores the level of dendritic spines of miR-132/212-deficient SCN neurons. Our results reveal that, by regulating the dendritic structure of SCN neurons through a MeCP2-dependent mechanism, miR-132/212 affects the capacity of the SCN to encode seasonal time.

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