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Loss of Nocturnin, a circadian deadenylase, confers resistance to hepatic steatosis and diet-induced obesity.

The mammalian circadian system consists of a central oscillator in the suprachiasmatic nucleus of the hypothalamus, which coordinates peripheral clocks in organs throughout the body. Although circadian clocks control the rhythmic expression of a large number of genes involved in metabolism and other aspects of circadian physiology, the consequences of genetic disruption of circadian-controlled pathways remain poorly defined. Here we report that the targeted disruption of Nocturnin (Ccrn4l) in mice, a gene that encodes a circadian deadenylase, confers resistance to diet-induced obesity. Mice lacking Nocturnin remain lean on high-fat diets, with lower body weight and reduced visceral fat. However, unlike lean lipodystrophic mouse models, these mice do not have fatty livers and do not exhibit increased activity or reduced food intake. Gene expression data suggest that Nocturnin knockout mice have deficits in lipid metabolism or uptake, in addition to changes in glucose and insulin sensitivity. Our data support a pivotal role for Nocturnin downstream of the circadian clockwork in the posttranscriptional regulation of genes necessary for nutrient uptake, metabolism, and storage.

Pubmed ID: 17517647


  • Green CB
  • Douris N
  • Kojima S
  • Strayer CA
  • Fogerty J
  • Lourim D
  • Keller SR
  • Besharse JC


Proceedings of the National Academy of Sciences of the United States of America

Publication Data

June 5, 2007

Associated Grants

  • Agency: NIGMS NIH HHS, Id: 2T32 GM008136-21
  • Agency: NIDDK NIH HHS, Id: DK063609
  • Agency: NEI NIH HHS, Id: EY02414
  • Agency: NEI NIH HHS, Id: EY11489
  • Agency: NIGMS NIH HHS, Id: GM076626

Mesh Terms

  • Animals
  • Azo Compounds
  • Biological Clocks
  • Blood Glucose
  • Body Temperature
  • Body Weight
  • Circadian Rhythm
  • Energy Metabolism
  • Fatty Liver
  • Feeding Behavior
  • Gene Expression Regulation
  • Gluconeogenesis
  • Immunity, Innate
  • Insulin
  • Lipids
  • Mice
  • Mice, Knockout
  • Nuclear Proteins
  • Obesity
  • Reverse Transcriptase Polymerase Chain Reaction
  • Suprachiasmatic Nucleus
  • Transcription Factors