脊髓性肌萎缩
生物
细胞生物学
RNA剪接
选择性拼接
SMN1型
肌萎缩侧索硬化
形状记忆合金*
运动神经元
剪接体
小核核糖核蛋白
核糖核蛋白
应力颗粒
遗传学
核糖核酸
信使核糖核酸
神经科学
病理
基因
翻译(生物学)
医学
组合数学
疾病
脊髓
数学
作者
Ravindra Singh,Matthew D. Howell,Eric W. Ottesen,Natalia N. Singh
标识
DOI:10.1016/j.bbagrm.2016.12.008
摘要
The multifunctional Survival Motor Neuron (SMN) protein is required for the survival of all organisms of the animal kingdom. SMN impacts various aspects of RNA metabolism through the formation and/or interaction with ribonucleoprotein (RNP) complexes. SMN regulates biogenesis of small nuclear RNPs, small nucleolar RNPs, small Cajal body-associated RNPs, signal recognition particles and telomerase. SMN also plays an important role in DNA repair, transcription, pre-mRNA splicing, histone mRNA processing, translation, selenoprotein synthesis, macromolecular trafficking, stress granule formation, cell signaling and cytoskeleton maintenance. The tissue-specific requirement of SMN is dictated by the variety and the abundance of its interacting partners. Reduced expression of SMN causes spinal muscular atrophy (SMA), a leading genetic cause of infant mortality. SMA displays a broad spectrum ranging from embryonic lethality to an adult onset. Aberrant expression and/or localization of SMN has also been associated with male infertility, inclusion body myositis, amyotrophic lateral sclerosis and osteoarthritis. This review provides a summary of various SMN functions with implications to a better understanding of SMA and other pathological conditions.
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