Dubowy Christine, Sehgal Amita
Cell and Molecular Biology Graduate Group, Biomedical Graduate Studies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104.
Chronobiology Program, Howard Hughes Medical Institute (HHMI), Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Genetics. 2017 Apr;205(4):1373-1397. doi: 10.1534/genetics.115.185157.
The advantages of the model organism , including low genetic redundancy, functional simplicity, and the ability to conduct large-scale genetic screens, have been essential for understanding the molecular nature of circadian (∼24 hr) rhythms, and continue to be valuable in discovering novel regulators of circadian rhythms and sleep. In this review, we discuss the current understanding of these interrelated biological processes in and the wider implications of this research. Clock genes and were first discovered in large-scale genetic screens developed in the 1970s. Feedback of and on their own transcription forms the core of the molecular clock, and accurately timed expression, localization, post-transcriptional modification, and function of these genes is thought to be critical for maintaining the circadian cycle. Regulators, including several phosphatases and kinases, act on different steps of this feedback loop to ensure strong and accurately timed rhythms. Approximately 150 neurons in the fly brain that contain the core components of the molecular clock act together to translate this intracellular cycling into rhythmic behavior. We discuss how different groups of clock neurons serve different functions in allowing clocks to entrain to environmental cues, driving behavioral outputs at different times of day, and allowing flexible behavioral responses in different environmental conditions. The neuropeptide PDF provides an important signal thought to synchronize clock neurons, although the details of how PDF accomplishes this function are still being explored. Secreted signals from clock neurons also influence rhythms in other tissues. SLEEP is, in part, regulated by the circadian clock, which ensures appropriate timing of sleep, but the amount and quality of sleep are also determined by other mechanisms that ensure a homeostatic balance between sleep and wake. Flies have been useful for identifying a large set of genes, molecules, and neuroanatomic loci important for regulating sleep amount. Conserved aspects of sleep regulation in flies and mammals include wake-promoting roles for catecholamine neurotransmitters and involvement of hypothalamus-like regions, although other neuroanatomic regions implicated in sleep in flies have less clear parallels. Sleep is also subject to regulation by factors such as food availability, stress, and social environment. We are beginning to understand how the identified molecules and neurons interact with each other, and with the environment, to regulate sleep. researchers can also take advantage of increasing mechanistic understanding of other behaviors, such as learning and memory, courtship, and aggression, to understand how sleep loss impacts these behaviors. Flies thus remain a valuable tool for both discovery of novel molecules and deep mechanistic understanding of sleep and circadian rhythms.
模式生物的优势,包括低基因冗余性、功能简单性以及进行大规模基因筛选的能力,对于理解昼夜节律(约24小时)的分子本质至关重要,并且在发现昼夜节律和睡眠的新型调节因子方面仍然具有重要价值。在这篇综述中,我们讨论了目前对这些相互关联的生物学过程的理解以及这项研究的更广泛意义。时钟基因和最早是在20世纪70年代开发的大规模基因筛选中发现的。和对其自身转录的反馈形成了分子时钟的核心,并且这些基因精确的定时表达、定位、转录后修饰和功能被认为对于维持昼夜节律周期至关重要。包括几种磷酸酶和激酶在内的调节因子作用于这个反馈环的不同步骤,以确保强烈且精确的定时节律。果蝇大脑中大约150个包含分子时钟核心成分的神经元共同作用,将这种细胞内的循环转化为节律性行为。我们讨论了不同组的时钟神经元如何在使时钟与环境线索同步、在一天中的不同时间驱动行为输出以及在不同环境条件下允许灵活的行为反应方面发挥不同的功能。神经肽PDF被认为提供了一个同步时钟神经元的重要信号,尽管PDF如何完成这一功能的细节仍在探索中。时钟神经元分泌的信号也会影响其他组织的节律。睡眠部分受昼夜节律时钟调节,昼夜节律时钟确保睡眠的适当时间,但睡眠的量和质量也由其他机制决定,这些机制确保睡眠和清醒之间的稳态平衡。果蝇对于识别大量调节睡眠量的重要基因、分子和神经解剖位点很有帮助。果蝇和哺乳动物睡眠调节的保守方面包括儿茶酚胺神经递质的促醒作用以及类似下丘脑区域的参与,尽管果蝇中涉及睡眠的其他神经解剖区域的相似之处不太明显。睡眠也受到食物供应、压力和社会环境等因素的调节。我们开始了解已识别的分子和神经元如何相互作用以及与环境相互作用来调节睡眠。研究人员还可以利用对其他行为,如学习和记忆、求偶和攻击行为的机制理解的增加来了解睡眠剥夺如何影响这些行为。因此,果蝇仍然是发现新分子以及深入理解睡眠和昼夜节律机制的宝贵工具。