Network Dynamics Mediate Circadian Clock Plasticity

Neuron. 2017 Jan 18;93(2):441-450. doi: 10.1016/j.neuron.2016.12.022. Epub 2017 Jan 5.


A circadian clock governs most aspects of mammalian behavior. Although its properties are in part genetically determined, altered light-dark environment can change circadian period length through a mechanism requiring de novo DNA methylation. We show here that this mechanism is mediated not via cell-autonomous clock properties, but rather through altered networking within the suprachiasmatic nuclei (SCN), the circadian "master clock," which is DNA methylated in region-specific manner. DNA methylation is necessary to temporally reorganize circadian phasing among SCN neurons, which in turn changes the period length of the network as a whole. Interruption of neural communication by inhibiting neuronal firing or by physical cutting suppresses both SCN reorganization and period changes. Mathematical modeling suggests, and experiments confirm, that this SCN reorganization depends upon GABAergic signaling. Our results therefore show that basic circadian clock properties are governed by dynamic interactions among SCN neurons, with neuroadaptations in network function driven by the environment.

Keywords: automation; autopatcher; in vivo; patch clamp; subcortical; thalamus; whole-cell.

MeSH terms

  • Action Potentials / physiology*
  • Animals
  • Circadian Clocks / genetics*
  • Circadian Clocks / physiology
  • Circadian Rhythm
  • DNA Methylation / genetics*
  • Light*
  • Male
  • Mice
  • Models, Theoretical
  • Neurons / cytology
  • Neurons / physiology*
  • Patch-Clamp Techniques
  • Period Circadian Proteins / genetics
  • Suprachiasmatic Nucleus / cytology
  • Suprachiasmatic Nucleus / metabolism*
  • Suprachiasmatic Nucleus / physiology
  • Thalamus / cytology
  • Thalamus / metabolism
  • gamma-Aminobutyric Acid / metabolism*


  • Per2 protein, mouse
  • Period Circadian Proteins
  • gamma-Aminobutyric Acid