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代谢型谷氨酸受体 1 突变导致自然短睡眠特征。

Mutations in Metabotropic Glutamate Receptor 1 Contribute to Natural Short Sleep Trait.

机构信息

Department of Neurology, University of California, San Francisco, San Francisco, CA 94143, USA.

Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94143, USA.

出版信息

Curr Biol. 2021 Jan 11;31(1):13-24.e4. doi: 10.1016/j.cub.2020.09.071. Epub 2020 Oct 15.

Abstract

Sufficient and efficient sleep is crucial for our health. Natural short sleepers can sleep significantly shorter than the average population without a desire for more sleep and without any obvious negative health consequences. In searching for genetic variants underlying the short sleep trait, we found two different mutations in the same gene (metabotropic glutamate receptor 1) from two independent natural short sleep families. In vitro, both of the mutations exhibited loss of function in receptor-mediated signaling. In vivo, the mice carrying the individual mutations both demonstrated short sleep behavior. In brain slices, both of the mutations changed the electrical properties and increased excitatory synaptic transmission. These results highlight the important role of metabotropic glutamate receptor 1 in modulating sleep duration.

摘要

充足和有效的睡眠对我们的健康至关重要。自然的短睡者可以比平均人群睡眠时间明显更短,而不会有更多睡眠的欲望,也没有任何明显的健康不良后果。在寻找导致短睡特征的遗传变异时,我们在两个独立的自然短睡家族中同一个基因(代谢型谷氨酸受体 1)中发现了两个不同的突变。在体外,这两种突变都表现出受体介导信号转导的功能丧失。在体内,携带单个突变的小鼠都表现出短睡眠行为。在脑片中,这两种突变都改变了电生理特性并增加了兴奋性突触传递。这些结果突出了代谢型谷氨酸受体 1在调节睡眠持续时间方面的重要作用。

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