Genetics is one of the various approaches adopted to understand and control mammalian sleep.Reverse genetics,which is usually applied to analyze sleep in gene-deficient mice,has been the mainstream field of genetic st...Genetics is one of the various approaches adopted to understand and control mammalian sleep.Reverse genetics,which is usually applied to analyze sleep in gene-deficient mice,has been the mainstream field of genetic studies on sleep for the past three decades and has revealed that various molecules,including orexin,are involved in sleep regulation.Recently,forward genetic studies in humans and mice have identified gene mutations responsible for heritable sleep abnormalities,such as SIK3,NALCN,DEC2,the neuropeptide S receptor,andβ1 adrenergic receptor.Furthermore,the protein kinase A-SIK3 pathway was shown to represent the intracellular neural signaling for sleep need.Large-scale genome-wide analyses of human sleep have been conducted,and many gene loci associated with individual differences in sleep have been found.The development of genome-editing technology and gene transfer by an adeno-associated virus has updated and expanded the genetic studies on mammals.These efforts are expected to elucidate the mechanisms of sleep–wake regulation and develop new therapeutic interventions for sleep disorders.展开更多
基金supported by the Ministry of Education,Culture,Sports,Science and Technology World Premier International Research Center Initiative to M.Y.Japan Society for the Promotion of Science KAKENHI(Grant Nos.17H06095 and 22H04918 to M.Y.and H.F.+1 种基金Grant Nos.17H04023,17H05583,and 20H00567 to H.F.)AMED(Grant No.JP21zf0127005 to M.Y.)。
文摘Genetics is one of the various approaches adopted to understand and control mammalian sleep.Reverse genetics,which is usually applied to analyze sleep in gene-deficient mice,has been the mainstream field of genetic studies on sleep for the past three decades and has revealed that various molecules,including orexin,are involved in sleep regulation.Recently,forward genetic studies in humans and mice have identified gene mutations responsible for heritable sleep abnormalities,such as SIK3,NALCN,DEC2,the neuropeptide S receptor,andβ1 adrenergic receptor.Furthermore,the protein kinase A-SIK3 pathway was shown to represent the intracellular neural signaling for sleep need.Large-scale genome-wide analyses of human sleep have been conducted,and many gene loci associated with individual differences in sleep have been found.The development of genome-editing technology and gene transfer by an adeno-associated virus has updated and expanded the genetic studies on mammals.These efforts are expected to elucidate the mechanisms of sleep–wake regulation and develop new therapeutic interventions for sleep disorders.
