电池极性
微管
肌张力障碍
亚细胞定位
基因产物
基因
神经突
神经科学
细胞生物学
生物
激酶
磷酸化
极性(国际关系)
遗传学
细胞
基因表达
体外
作者
Giulia Ferrari Toninelli,PierFranco Spano,Maurizio Memo
出处
期刊:PubMed
日期:2003-05-23
卷期号:18 (1): 7-10
被引量:9
摘要
Early-onset primary dystonia is an inherited disorder characterized by involuntary twisting, repetitive movements and abnormal postures. It has recently been demonstrated that the DYT1 gene is the most relevant gene associated with primary generalized dystonia. The DYT1 gene product is a 332-aminoacid long protein, termed TorsinA, whose function is still not clear. Based on the results obtained in other species, we proposed that TorsinA, similarly to OOC-5 in nematodes, directs and/or stabilizes the subcellular localization of specific kinases, which may in turn phosphorylate microtubule associated proteins, such as tau. In this way, TorsinA may contribute to maintaining the appropriate site-directed polarization and control neurite outgrowth.
科研通智能强力驱动
Strongly Powered by AbleSci AI