Department of Biology and Center for Biological Clocks Research, Texas A&MUniversity, College Station, USA.
Adv Genet. 2011;74:141-73. doi: 10.1016/B978-0-12-387690-4.00005-2.
A genetic screen for mutants that alter circadian rhythms in Drosophila identified the first clock gene-the period (per) gene. The per gene is a central player within a transcriptional feedback loop that represents the core mechanism for keeping circadian time in Drosophila and other animals. The per feedback loop, or core loop, is interlocked with the Clock (Clk) feedback loop, but whether the Clk feedback loop contributes to circadian timekeeping is not known. A series of distinct molecular events are thought to control transcriptional feedback in the core loop. The time it takes to complete these events should take much less than 24h, thus delays must be imposed at different steps within the core loop. As new clock genes are identified, the molecular mechanisms responsible for these delays have been revealed in ever-increasing detail and provide an in-depth accounting of how transcriptional feedback loops keep circadian time. The phase of these feedback loops shifts to maintain synchrony with environmental cycles, the most reliable of which is light. Although a great deal is known about cell-autonomous mechanisms of light-induced phase shifting by CRYPTOCHROME (CRY), much less is known about non-cell autonomous mechanisms. CRY mediates phase shifts through an uncharacterized mechanism in certain brain oscillator neurons and carries out a dual role as a photoreceptor and transcription factor in other tissues. Here, I review how transcriptional feedback loops function to keep time in Drosophila, how they impose delays to maintain a 24-h cycle, and how they maintain synchrony with environmental light:dark cycles. The transcriptional feedback loops that keep time in Drosophila are well conserved in other animals, thus what we learn about these loops in Drosophila should continue to provide insight into the operation of analogous transcriptional feedback loops in other animals.
一个用于鉴定改变果蝇昼夜节律的突变体的遗传筛选,发现了第一个生物钟基因——周期(per)基因。per 基因是一个转录反馈回路中的核心成员,该回路代表了在果蝇和其他动物中保持昼夜节律的核心机制。per 反馈回路或核心回路与 Clock(Clk)反馈回路相互锁定,但 Clk 反馈回路是否有助于生物钟计时尚不清楚。一系列不同的分子事件被认为控制着核心回路中的转录反馈。完成这些事件所需的时间应该远小于 24 小时,因此必须在核心回路的不同步骤中施加延迟。随着新的生物钟基因的鉴定,核心回路中不同步骤的延迟机制已被越来越详细地揭示出来,为转录反馈回路如何保持昼夜节律提供了深入的解释。这些反馈回路的相位会发生变化,以与环境周期保持同步,其中最可靠的是光。尽管人们对隐花色素(CRY)诱导的光相移的细胞自主机制了解很多,但对非细胞自主机制了解甚少。CRY 通过特定脑振荡器神经元中的未被表征的机制介导相移,并在其他组织中发挥作为光受体和转录因子的双重作用。在这里,我回顾了转录反馈回路如何在果蝇中保持时间,它们如何施加延迟以维持 24 小时周期,以及它们如何与环境光暗周期保持同步:转录反馈回路在果蝇中保持时间的机制在其他动物中很好地保守,因此我们在果蝇中了解这些回路应该继续为其他动物中类似的转录反馈回路的运作提供深入的见解。