Department of System Biology, Graduate School of Pharmaceutical Sciences, Kyoto University, 46-29 Yoshida-Shimo-Adachi-cho, Kyoto 606-8501, Japan.
Cell Rep. 2012 Apr 19;1(4):341-9. doi: 10.1016/j.celrep.2012.03.001. Epub 2012 Apr 20.
The synthesis of nucleotides in the body is centrally controlled by the liver, via salvage or de novo synthesis. We reveal a pervasive circadian influence on hepatic nucleotide metabolism, from rhythmic gene expression of rate-limiting enzymes to oscillating nucleotide metabolome in wild-type (WT) mice. Genetic disruption of the hepatic clock leads to aberrant expression of these enzymes, together with anomalous nucleotide rhythms, such as constant low levels of ATP with an excess in uric acid, the degradation product of purines. These results clearly demonstrate that the hepatic circadian clock orchestrates nucleotide synthesis and degradation. This circadian metabolome timetable, obtained using state-of-the-art capillary electrophoresis time-of-flight mass spectrometry, will guide further investigations in nucleotide metabolism-related disorders.
体内核苷酸的合成受到肝脏的中央控制,通过补救途径或从头合成。我们揭示了肝脏核苷酸代谢存在普遍的昼夜节律影响,从限速酶的节律性基因表达到野生型(WT)小鼠核苷酸代谢组的波动。肝时钟的遗传破坏导致这些酶的异常表达,以及异常的核苷酸节律,例如 ATP 水平持续低而尿酸(嘌呤的降解产物)过量。这些结果清楚地表明,肝脏生物钟协调核苷酸的合成和降解。使用最先进的毛细管电泳飞行时间质谱法获得的这种昼夜代谢组时间表将指导核苷酸代谢相关疾病的进一步研究。