脊髓性肌萎缩
生物
细胞生物学
粒体自噬
自噬
运动神经元
好斗的
神经退行性变
泛素
生物发生
神经科学
遗传学
基因
脊髓
细胞凋亡
病理
疾病
医学
作者
Helena Chaytow,Yu-Ting Huang,Thomas H. Gillingwater,Kiterie M. E. Faller
标识
DOI:10.1007/s00018-018-2849-1
摘要
Ever since loss of survival motor neuron (SMN) protein was identified as the direct cause of the childhood inherited neurodegenerative disorder spinal muscular atrophy, significant efforts have been made to reveal the molecular functions of this ubiquitously expressed protein. Resulting research demonstrated that SMN plays important roles in multiple fundamental cellular homeostatic pathways, including a well-characterised role in the assembly of the spliceosome and biogenesis of ribonucleoproteins. More recent studies have shown that SMN is also involved in other housekeeping processes, including mRNA trafficking and local translation, cytoskeletal dynamics, endocytosis and autophagy. Moreover, SMN has been shown to influence mitochondria and bioenergetic pathways as well as regulate function of the ubiquitin–proteasome system. In this review, we summarise these diverse functions of SMN, confirming its key role in maintenance of the homeostatic environment of the cell.
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