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节律基因 Per2/Dec 突变小鼠光控活动起始和恢复自由运行视交叉上核节律。

Advanced light-entrained activity onsets and restored free-running suprachiasmatic nucleus circadian rhythms in per2/dec mutant mice.

机构信息

Circadian Rhythms Group , Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.

出版信息

Chronobiol Int. 2011 Nov;28(9):737-50. doi: 10.3109/07420528.2011.607374.

DOI:10.3109/07420528.2011.607374
PMID:22080784
Abstract

Many behavioral and physiological processes display diurnal (24-h) rhythms controlled by an internal timekeeping system?the circadian clock. In mammals, a circadian pacemaker is located in the suprachiasmatic nucleus (SCN) of the hypothalamus and synchronizes peripheral oscillators found in most other tissues with the external light-dark (LD) cycle. At the molecular level, circadian clocks are regulated by transcriptional translational feedback loops (TTLs) involving a set of clock genes. The mammalian core TTL includes the transcriptional modulators PER?(1?3) and CRY?(1/2) that inhibit their own expression by interaction with CLOCK/NPAS2 and BMAL1 (ARNTL). The basic helix-loop-helix transcription factors DEC1 (BHLHE40) and DEC2 (BHLHE41) can interact with this core TTL, forming an accessory feedback mechanism. The authors measured circadian locomotor behavior and clock gene expression in the SCN of Per2/Dec double- and triple-mutant mice to analyze the functional interaction of PER2 and DEC feedback on circadian pacemaker function in the SCN. The data suggest a synergistic interaction of Per2 and Dec1/2 in activity entrainment to a standard LD cycle, correlating with a cumulative deficiency in negative-masking capacities in Per2/Dec double- and triple-mutant mice and suggesting an involvement of Per2-Dec1/2 interactivity in activity-onset regulation and masking under LD, but not under constant conditions. In contrast, under constant darkness (DD) conditions, a deletion of either Dec1 or Dec2 partially rescued the Per2 mutant short-period/arrhythmicity phenotype, accompanied by a restoration of time-of-day effects on clock gene expression in the SCN. Together, these results show an interaction of Per2 and Dec1/2 feedback processes in the SCN with differential modes of interactivity under entrained and free-run conditions. (Author correspondence: henrik.oster@mpibpc.mpg.de ).

摘要

许多行为和生理过程表现出昼夜(24 小时)节律,受内部计时系统——生物钟的控制。在哺乳动物中,生物钟位于下丘脑的视交叉上核(SCN),并使大多数其他组织中的外周振荡器与外部明暗(LD)周期同步。在分子水平上,生物钟受涉及一组时钟基因的转录翻译反馈环(TTLs)调节。哺乳动物核心 TTL 包括转录调节剂 PER?(1?3)和 CRY?(1/2),它们通过与 CLOCK/NPAS2 和 BMAL1(ARNTL)相互作用来抑制自身表达。碱性螺旋-环-螺旋转录因子 DEC1(BHLHE40)和 DEC2(BHLHE41)可以与这个核心 TTL 相互作用,形成一个辅助反馈机制。作者测量了 Per2/Dec 双突变和三突变小鼠 SCN 中的昼夜运动行为和时钟基因表达,以分析 PER2 和 DEC 反馈对 SCN 中昼夜起搏器功能的功能相互作用。数据表明,在标准 LD 周期中,Per2 和 Dec1/2 在活动同步方面存在协同相互作用,与 Per2/Dec 双突变和三突变小鼠中负掩蔽能力的累积缺乏相关,表明 Per2-Dec1/2 相互作用参与了 LD 下活动起始的调节和掩蔽,但不在恒定条件下。相比之下,在持续黑暗(DD)条件下,缺失 Dec1 或 Dec2 中的任一个都部分挽救了 Per2 突变体的短周期/节律性表型,同时恢复了 SCN 中时钟基因表达的时间效应。总之,这些结果表明,Per2 和 Dec1/2 反馈过程在 SCN 中相互作用,在同步和自由运行条件下具有不同的相互作用模式。(作者通讯:henrik.oster@mpibpc.mpg.de)。

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