Title of article :
Altered Body Weight Regulation in CK1𝜀 Null and tau Mutant Mice on Regular Chow and High Fat Diets
Author/Authors :
Zhou, Lili Center for Sleep and Circadian Biology - Northwestern University - Evanston - IL 60208 - USA - Department of Neurobiology - Northwestern University - Evanston - IL 60208 - USA , Summa, Keith C Center for Sleep and Circadian Biology - Northwestern University - Evanston - IL 60208 - USA - Department of Neurobiology - Northwestern University - Evanston - IL 60208 - USA , Olker, Christopher Center for Sleep and Circadian Biology - Northwestern University - Evanston - IL 60208 - USA - Department of Neurobiology - Northwestern University - Evanston - IL 60208 - USA , Vitaterna, Martha H Center for Sleep and Circadian Biology - Northwestern University - Evanston - IL 60208 - USA - Department of Neurobiology - Northwestern University - Evanston - IL 60208 - USA , Turek, Fred W Center for Sleep and Circadian Biology - Northwestern University - Evanston - IL 60208 - USA - Department of Neurobiology - Northwestern University - Evanston - IL 60208 - USA
Pages :
10
From page :
1
To page :
10
Abstract :
Disruption of circadian rhythms results in metabolic dysfunction. Casein kinase 1 epsilon (CK1𝜀) is a canonical circadian clock gene. Null and tau mutations in CK1𝜀 show distinct effects on circadian period. To investigate the role of CK1𝜀 in body weight regulation under both regular chow (RC) and high fat (HF) diet conditions, we examined body weight on both RC and HF diets in CK1𝜀 −/− and CK1𝜀 𝑡𝑎𝑢/𝑡𝑎𝑢 mice on a standard 24 hr light-dark (LD) cycle. Given the abnormal entrainment of CK1𝜀 𝑡𝑎𝑢/𝑡𝑎𝑢 mice on a 24 hr LD cycle, a separate set of CK1𝜀 𝑡𝑎𝑢/𝑡𝑎𝑢 mice were tested under both diet conditions on a 20 hr LD cycle, which more closely matches their endogenous period length. On the RC diet, both CK1𝜀 −/− and CK1𝜀 𝑡𝑎𝑢/𝑡𝑎𝑢 mutants on a 24 hr LD cycle and CK1𝜀 𝑡𝑎𝑢/𝑡𝑎𝑢 mice on a 20 hr LD cycle exhibited significantly lower body weights, despite similar overall food intake and activity levels. On the HF diet, CK1𝜀 𝑡𝑎𝑢/𝑡𝑎𝑢 mice on a 20 hr LD cycle were protected against the development of HF diet-induced excess weight gain. These results provide additional evidence supporting a link between circadian rhythms and energy regulation at the genetic level, particularly highlighting CK1𝜀 involved in the integration of circadian biology and metabolic physiology.
Keywords :
regular chow (RC) , high fat (HF) , light-dark (LD) cycle , Casein kinase 1 epsilon (CK1𝜀) , Body Weight Regulation , tau Mutant Mice , Regular Chow
Journal title :
Genetics Research International
Serial Year :
2016
Full Text URL :
Record number :
2608300
Link To Document :
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