Pellegrino Renata, Kavakli Ibrahim Halil, Goel Namni, Cardinale Christopher J, Dinges David F, Kuna Samuel T, Maislin Greg, Van Dongen Hans P A, Tufik Sergio, Hogenesch John B, Hakonarson Hakon, Pack Allan I
Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA ; Center for Sleep and Circadian Neurobiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA ; Departamento de Psicobiologia, Universidade Federal de São Paulo, UNIFESP, São Paulo, Brazil.
Departments of Chemical and Biological Eng. and Molecular Biology and Genetics, Koc University, Rumelifeneri Yolu, Sariyer-Istanbul, Turkey.
Sleep. 2014 Aug 1;37(8):1327-36. doi: 10.5665/sleep.3924.
Earlier work described a mutation in DEC2 also known as BHLHE41 (basic helix-loophelix family member e41) as causal in a family of short sleepers, who needed just 6 h sleep per night. We evaluated whether there were other variants of this gene in two well-phenotyped cohorts.
Sequencing of the BHLHE41 gene, electroencephalographic data, and delta power analysis and functional studies using cell-based luciferase.
We identified new variants of the BHLHE41 gene in two cohorts who had either acute sleep deprivation (n = 200) or chronic partial sleep deprivation (n = 217). One variant, Y362H, at another location in the same exon occurred in one twin in a dizygotic twin pair and was associated with reduced sleep duration, less recovery sleep following sleep deprivation, and fewer performance lapses during sleep deprivation than the homozygous twin. Both twins had almost identical amounts of non rapid eye movement (NREM) sleep. This variant reduced the ability of BHLHE41 to suppress CLOCK/BMAL1 and NPAS2/BMAL1 transactivation in vitro. Another variant in the same exome had no effect on sleep or response to sleep deprivation and no effect on CLOCK/BMAL1 transactivation. Random mutagenesis identified a number of other variants of BHLHE41 that affect its function.
There are a number of mutations of BHLHE41. Mutations reduce total sleep while maintaining NREM sleep and provide resistance to the effects of sleep loss. Mutations that affect sleep also modify the normal inhibition of BHLHE41 of CLOCK/BMAL1 transactivation. Thus, clock mechanisms are likely involved in setting sleep length and the magnitude of sleep homeostasis.
Pellegrino R, Kavakli IH, Goel N, Cardinale CJ, Dinges DF, Kuna ST, Maislin G, Van Dongen HP, Tufik S, Hogenesch JB, Hakonarson H, Pack AI. A novel BHLHE41 variant is associated with short sleep and resistance to sleep deprivation in humans. SLEEP 2014;37(8):1327-1336.
早期研究描述了DEC2(也称为BHLHE41,即碱性螺旋-环-螺旋家族成员e41)中的一种突变,该突变导致一个短睡眠家族的出现,这些人每晚仅需6小时睡眠。我们评估了在两个表型良好的队列中该基因是否存在其他变体。
对BHLHE41基因进行测序、脑电图数据收集、δ波功率分析以及使用基于细胞的荧光素酶进行功能研究。
我们在两个队列中鉴定出了BHLHE41基因的新变体,其中一个队列有急性睡眠剥夺(n = 200),另一个队列有慢性部分睡眠剥夺(n = 217)。一个变体Y362H出现在同一条外显子的另一个位置,在一对异卵双胞胎中的一个身上出现,与睡眠时间缩短、睡眠剥夺后恢复睡眠较少以及睡眠剥夺期间的表现失误较少有关,与纯合子双胞胎相比。这对双胞胎的非快速眼动(NREM)睡眠量几乎相同。该变体在体外降低了BHLHE41抑制CLOCK/BMAL1和NPAS2/BMAL1转录激活的能力。同一条外显子中的另一个变体对睡眠或睡眠剥夺反应没有影响,对CLOCK/BMAL1转录激活也没有影响。随机诱变鉴定出了一些其他影响BHLHE41功能的变体。
BHLHE41存在多种突变。这些突变减少了总睡眠时间,同时维持了NREM睡眠,并提供了对睡眠丧失影响的抵抗力。影响睡眠的突变也改变了BHLHE41对CLOCK/BMAL1转录激活的正常抑制作用。因此,生物钟机制可能参与设定睡眠时间和睡眠稳态的程度。
Pellegrino R, Kavakli IH, Goel N, Cardinale CJ, Dinges DF, Kuna ST, Maislin G, Van Dongen HP, Tufik S, Hogenesch JB, Hakonarson H, Pack AI. 一种新型BHLHE41变体与人类短睡眠和抗睡眠剥夺有关。《睡眠》2014年;37(8):1327 - 1336。