Neurology Research, 115 Broadway, Bio 6 Building, Biogen, Cambridge, MA 02142, USA.
Neurology Research, 115 Broadway, Bio 6 Building, Biogen, Cambridge, MA 02142, USA.
Exp Neurol. 2015 Dec;274(Pt A):72-9. doi: 10.1016/j.expneurol.2015.06.024. Epub 2015 Jul 6.
Genetic underpinnings for sleep disorders in humans remain poorly identified, investigated and understood. This is due to the inherent complexity of sleep and a disruption of normal sleep parameters in a number of neurological disorders. On the other hand, there have been steady and remarkable developments in the investigation of sleep using model organisms such as Drosophila. These studies have illuminated conserved genetic pathways, neural circuits and intra-cellular signaling modules in the regulation of sleep. Additionally, work in model systems is beginning to clarify the role of the circadian clock and basal sleep need in this process. There have also been initial efforts to directly model sleep disorders in flies in a few instances where a genetic basis has been suspected. Here, we discuss the opportunities and limitations of studying sleep disorders in Drosophila and propose that a greater convergence of basic sleep research in model organisms and human genetics should catalyze better understanding of sleep disorders and generate viable therapeutic options.
人类睡眠障碍的遗传基础仍未得到充分的识别、研究和理解。这是由于睡眠的固有复杂性以及许多神经紊乱疾病中正常睡眠参数的中断。另一方面,使用果蝇等模式生物对睡眠进行研究已经取得了稳定而显著的进展。这些研究揭示了调节睡眠的保守遗传途径、神经回路和细胞内信号模块。此外,在模型系统中的工作也开始阐明生物钟和基础睡眠需求在这个过程中的作用。在少数情况下,已经有初步努力直接在果蝇中模拟睡眠障碍,这些情况被怀疑存在遗传基础。在这里,我们讨论了在果蝇中研究睡眠障碍的机会和局限性,并提出,在模式生物的基础睡眠研究和人类遗传学之间进行更大的融合,应该能够促进对睡眠障碍的更好理解,并产生可行的治疗选择。