SIRT1 mediates central circadian control in the SCN by a mechanism that decays with aging.

SUMMARY SIRT1 is a NAD + -dependent protein deacetylase that governs many physiological pathways, including circadian rhythm in peripheral tissues. Here, we showthatSIRT1inthebraingovernscentralcircadian control by activating the transcription of the two major circadian regulators, BMAL1 and CLOCK. This activation comprises an amplifying circadian loop involving SIRT1, PGC-1a, and Nampt. In aged wildtype mice, SIRT1 levels in the suprachiasmatic nucleus are decreased, as are those of BMAL1 and PER2, giving rise to a longer intrinsic period, a more disrupted activity pattern, and an inability to adapt to changes in the light entrainment schedule. Young mice lacking brain SIRT1 phenocopy these agingdependent circadian changes, whereas mice that overexpress SIRT1 in the brain are protected from the effects of aging. Our findings indicate that SIRT1 activates the central pacemaker to maintain robust circadian control in young animals, and a decay in this activity may play an important role in aging.