Lack of food anticipation in Per2 mutant mice

Curr Biol. 2006 Oct 24;16(20):2016-22. doi: 10.1016/j.cub.2006.08.053.


Predicting time of food availability is key for survival in most animals. Under restricted feeding conditions, this prediction is manifested in anticipatory bouts of locomotor activity and body temperature. This process seems to be driven by a food-entrainable oscillator independent of the main, light-entrainable clock located in the suprachiasmatic nucleus (SCN) of the hypothalamus . Although the SCN clockwork involves self-sustaining transcriptional and translational feedback loops based on rhythmic expression of mRNA and proteins of clock genes , the molecular mechanisms responsible for food anticipation are not well understood. Period genes Per1 and Per2 are crucial for the SCN's resetting to light . Here, we investigated the role of these genes in circadian anticipatory behavior by studying rest-activity and body-temperature rhythms of Per1 and Per2 mutant mice under restricted feeding conditions. We also monitored expression of clock genes in the SCN and peripheral tissues. Whereas wild-type and Per1 mutant mice expressed regular food-anticipatory activity, Per2 mutant mice did not show food anticipation. In peripheral tissues, however, phase shifts of clock-gene expression in response to timed food restriction were comparable in all genotypes. In conclusion, a mutation in Per2 abolishes anticipation of mealtime, without interfering with peripheral synchronization by feeding cycles.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Biological Clocks / physiology*
  • Body Composition
  • Body Temperature
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Circadian Rhythm / physiology*
  • DNA Primers
  • Feeding Behavior / physiology*
  • In Situ Hybridization
  • Mice
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Period Circadian Proteins
  • Physical Exertion / physiology
  • Polymerase Chain Reaction
  • Suprachiasmatic Nucleus / metabolism
  • Suprachiasmatic Nucleus / physiology*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*


  • Cell Cycle Proteins
  • DNA Primers
  • Nuclear Proteins
  • Per2 protein, mouse
  • Period Circadian Proteins
  • Transcription Factors