Ito Daisuke, Yagi Takuya, Suzuki Norihiro
Department of Neurology, School of Medicine, Keio University.
Rinsho Shinkeigaku. 2011 Nov;51(11):1186-8. doi: 10.5692/clinicalneurol.51.1186.
The Seipin/BSCL2 gene was originally identified as a loss-of-function gene for congenital generalized lipodystrophy type 2, a condition characterized by severe lipoatrophy, insulin resistance, and hypertriglyceridemia. Whereas gain-of-toxic-function mutations (namely, mutations N88S and S90L) in the seipin gene have been identified in autosomal dominant motor neuron diseases such as Silver syndrome/spastic paraplegia 17 (SPG17) and distal hereditary motor neuropathy type V. Detailed phenotypic analyses have revealed that upper motor neurons, lower motor neurons and peripheral motor axons are variously affected in patients with these mutations. We recently showed that the N88S and S90L mutations disrupt the N-glycosylation motif, enhance ubiquitination, and appear to result in proteins that are improperly folded, leading to accumulation of the mutant protein in the endoplasmic reticulum (ER). We also showed that expression of mutant in cultured cells activates the UPR pathway and induces cell death, suggesting that seipinopathy is tightly associated with ER stress, which has recently been reported to be associated with other neurodegenerative diseases. Further study of the pathological mechanisms of the mutant forms of seipin may lead to important new insights into motor neuron diseases, including other spastic paraplegia diseases and amyotrophic lateral sclerosis.
Seipin/BSCL2基因最初被鉴定为2型先天性全身性脂肪营养不良的功能丧失基因,该病症的特征为严重脂肪萎缩、胰岛素抵抗和高甘油三酯血症。而在常染色体显性运动神经元疾病如Silver综合征/痉挛性截瘫17型(SPG17)和V型远端遗传性运动神经病中,已鉴定出seipin基因的功能获得性毒性突变(即N88S和S90L突变)。详细的表型分析表明,这些突变患者的上运动神经元、下运动神经元和周围运动轴突受到不同程度的影响。我们最近发现,N88S和S90L突变破坏了N-糖基化基序,增强了泛素化作用,似乎导致蛋白质折叠不当,致使突变蛋白在内质网(ER)中积累。我们还发现,在培养细胞中表达突变体可激活未折叠蛋白反应(UPR)途径并诱导细胞死亡,这表明seipin病与内质网应激密切相关,最近有报道称内质网应激与其他神经退行性疾病有关。对seipin突变形式病理机制的进一步研究可能会为运动神经元疾病带来重要的新见解,包括其他痉挛性截瘫疾病和肌萎缩侧索硬化症。