Perutz M F, Windle A H
MRC Laboratory of Molecular Biology, Cambridge, UK.
Nature. 2001 Jul 12;412(6843):143-4. doi: 10.1038/35084141.
Neurodegenerative diseases resulting from expanded repeat sequences of glutamine residues are associated with the formation of protein aggregates in the cell nuclei of the affected neurons, but whether these are pathogenic is controversial. Recent observations indicate that the ages of onset of these diseases are exponential functions of the repeat lengths and that the probability of neural death is constant with time. The only process known to us that could give rise to such behaviour is nucleation of the aggregates.
由谷氨酰胺残基的重复序列扩增导致的神经退行性疾病与受影响神经元细胞核中蛋白质聚集体的形成有关,但这些聚集体是否具有致病性仍存在争议。最近的观察结果表明,这些疾病的发病年龄是重复长度的指数函数,并且神经死亡的概率随时间恒定。我们所知的唯一能产生这种行为的过程是聚集体的成核作用。