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The role of survival motor neuron protein (SMN) in protein homeostasis

期刊

CELLULAR AND MOLECULAR LIFE SCIENCES
卷 75, 期 21, 页码 3877-3894

出版社

SPRINGER BASEL AG
DOI: 10.1007/s00018-018-2849-1

关键词

Spinal muscular atrophy; Ribonucleoprotein; Translation; Cytoskeleton; Ubiquitin; Bioenergetic pathway

资金

  1. UK SMA Research Consortium (SMA Trust)
  2. MND Scotland
  3. SMA Europe

向作者/读者索取更多资源

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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