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Inactivation of Cipc alters the expression of Per1 but not circadian rhythms in mice 被引量:2

Inactivation of Cipc alters the expression of Per1 but not circadian rhythms in mice
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摘要 Circadian clocks are comprised of self-sustained transcriptional/translational feedback loops, which regulate the rhythms of physiology and behavior in mammals. CLOCK-interacting protein, Circadian(CIPC), has been indicated as an additional negative-feedback regulator of the circadian clock in vitro, although its physiological roles in circadian clock are unknown. Here, we generated Cipc homozygous knockout(Cipc-/-) mice and assessed the resultant circadian phenotypes. Surprisingly, the m RNA expression profiles of core clock genes in the liver of Cipc-/- mice showed no significant differences from that in wild-type mice except for Per1. Cipc-/- mice displayed normal locomotor rhythm and entrained activity pattern in both 12:12 light-dark cycle and constant dark cycle. Furthermore, deletion of Cipc in lungs and adipose tissues did not influence their peripheral clock. The results from this work provided more conclusive data suggesting that CIPC is not critically required for basic clock function. Circadian clocks are comprised of self-sustained transcriptional/translational feedback loops, which regulate the rhythms of physiology and behavior in mammals. CLOCK-interacting protein, Circadian (CIPC), has been indicated as an additional negative-feedback regulator of the circadian clock in vitro, although its physiological roles in circadian clock are unknown. Here, we generated Cipc homozygous knockout (Cipc^-/-) mice and assessed the resultant circadian phenotypes. Surprisingly, the mRNA expression profiles of core clock genes in the liver of Cipc^-/- mice showed no significant differences from that in wild-type mice except for Per1. Cipc^-/- mice displayed normal locomotor rhythm and entrained activity pattern in both 12:12 light-dark cycle and constant dark cycle. Furthermore, deletion of Cipc in lungs and adipose tissues did not influence their peripheral clock. The results from this work provided more conclusive data suggesting that CIPC is not critically required for basic clock function.
出处 《Science China(Life Sciences)》 SCIE CAS CSCD 2015年第4期368-372,共5页 中国科学(生命科学英文版)
基金 supported by the National Natural Science Foundation of China(31171343 and 31230049 to Xu Ying) Ministry of Science and Technology(2006BAI23B00 to Xu Ying and Gao Xiang)
关键词 CIPC circadian clock animal model 生理节律 小鼠 Perl 失活 体内 生物钟 反馈回路 哺乳动物
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