Diverse role of survival motor neuron protein

被引:218
作者
Singh, Ravindra N. [1 ]
Howell, Matthew D. [1 ]
Ottesen, Eric W. [1 ]
Singh, Natalia N. [1 ]
机构
[1] Iowa State Univ, Dept Biomed Sci, Ames, IA 50011 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2017年 / 1860卷 / 03期
基金
美国国家卫生研究院;
关键词
Spinal muscular atrophy; SMA; Survival Motor Neuron; SMN; Splicing; snRNP biogenesis; snoRNP biogenesis; SBP2; Telomerase; TERC; TERT; TMG; Transcription; DNA repair; Selenoprotein; Signal recognition particle; Cajal body; Gem; SPINAL MUSCULAR-ATROPHY; ACTIN MESSENGER-RNA; SMALL NUCLEAR RIBONUCLEOPROTEIN; DETERMINING GENE-PRODUCT; C-TERMINAL DOMAIN; SMN TUDOR DOMAIN; MOUSE MODEL; CAJAL BODIES; BINDING PROTEIN; CRITICAL EXON;
D O I
10.1016/j.bbagrm.2016.12.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:299 / 315
页数:17
相关论文
共 286 条
[1]   The intriguing case of motor neuron disease: ALS and SMA come closer [J].
Achsel, Tilmann ;
Barabino, Silvia ;
Cozzolino, Mauro ;
Carri, Maria Teresa .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2013, 41 :1593-1597
[2]   Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality [J].
Ackermann, Bastian ;
Kroeber, Sandra ;
Torres-Benito, Laura ;
Borgmann, Anke ;
Peters, Miriam ;
Barkooie, Seyyed Mohsen Hosseini ;
Tejero, Rocio ;
Jakubik, Miriam ;
Schreml, Julia ;
Milbradt, Janine ;
Wunderlich, Thomas F. ;
Riessland, Markus ;
Tabares, Lucia ;
Wirth, Brunhilde .
HUMAN MOLECULAR GENETICS, 2013, 22 (07) :1328-1347
[3]   Molecular Mechanisms of Neurodegeneration in Spinal Muscular Atrophy [J].
Ahmad, Saif ;
Bhatia, Kanchan ;
Kannan, Annapoorna ;
Gangwani, Laxman .
JOURNAL OF EXPERIMENTAL NEUROSCIENCE, 2016, 10 :39-49
[4]   The zinc finger protein ZPR1 is a potential modifier of spinal muscular atrophy [J].
Ahmad, Saif ;
Wang, Yi ;
Shaik, Gouse M. ;
Burghes, Arthur H. ;
Gangwani, Laxman .
HUMAN MOLECULAR GENETICS, 2012, 21 (12) :2745-2758
[5]   Interaction of survival of motor neuron (SMN) and HuD proteins with mRNA cpg15 rescues motor neuron axonal deficits [J].
Akten, Bikem ;
Kye, Min Jeong ;
Hao, Le T. ;
Wertz, Mary H. ;
Singh, Sasha ;
Nie, Duyu ;
Huang, Jia ;
Merianda, Tanuja T. ;
Twiss, Jeffery L. ;
Beattie, Christine E. ;
Steen, Judith A. J. ;
Sahin, Mustafa .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (25) :10337-10342
[6]   Promoter directionality is controlled by U1 snRNP and polyadenylation signals [J].
Almada, Albert E. ;
Wu, Xuebing ;
Kriz, Andrea J. ;
Burge, Christopher B. ;
Sharp, Phillip A. .
NATURE, 2013, 499 (7458) :360-U141
[7]   Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients [J].
Amara, Abdelbasset ;
Adala, Labiba ;
Ben Charfeddine, Ilhem ;
Mamai, Ons ;
Mili, Amira ;
Ben Lazreg, Taheni ;
H'mida, Dorra ;
Amri, Fathi ;
Salem, Najla ;
Boughammura, Lamia ;
Saad, Ali ;
Gribaa, Moez .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2012, 16 (02) :167-174
[8]   Stress granules, P-bodies and cancer [J].
Anderson, Paul ;
Kedersha, Nancy ;
Ivanov, Pavel .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2015, 1849 (07) :861-870
[9]  
[Anonymous], HUM MOL GENET
[10]  
[Anonymous], 2016, J MOL BIOL