Goodchild Rose E, Kim Connie Eunji, Dauer William T
Department of Neurology, Columbia University, New York, New York 10032, USA.
Neuron. 2005 Dec 22;48(6):923-32. doi: 10.1016/j.neuron.2005.11.010.
An enigmatic feature of many genetic diseases is that mutations in widely expressed genes cause tissue-specific illness. One example is DYT1 dystonia, a neurodevelopmental disease caused by an in-frame deletion (Deltagag) in the gene encoding torsinA. Here we show that neurons from both torsinA null (Tor1a(-/-)) and homozygous disease mutant "knockin" mice (Tor1a(Deltagag/Deltagag)) contain severely abnormal nuclear membranes, although non-neuronal cell types appear normal. These membrane abnormalities develop in postmigratory embryonic neurons and subsequently worsen with further neuronal maturation, a finding evocative of the developmental dependence of DYT1 dystonia. These observations demonstrate that neurons have a unique requirement for nuclear envelope localized torsinA function and suggest that loss of this activity is a key molecular event in the pathogenesis of DYT1 dystonia.
许多遗传疾病的一个神秘特征是,广泛表达的基因中的突变会导致组织特异性疾病。一个例子是DYT1肌张力障碍,这是一种神经发育疾病,由编码扭转蛋白A的基因中的框内缺失(Deltagag)引起。在这里,我们表明,来自扭转蛋白A基因敲除(Tor1a(-/-))和纯合疾病突变“敲入”小鼠(Tor1a(Deltagag/Deltagag))的神经元都含有严重异常的核膜,而非神经元细胞类型看起来正常。这些膜异常在迁移后的胚胎神经元中出现,随后随着神经元的进一步成熟而恶化,这一发现让人联想到DYT1肌张力障碍的发育依赖性。这些观察结果表明,神经元对核膜定位的扭转蛋白A功能有独特需求,并表明这种活性的丧失是DYT1肌张力障碍发病机制中的关键分子事件。