RNA-binding proteins in microsatellite expansion disorders: Mediators of RNA toxicity

被引:70
作者
Echeverria, Gloria V. [2 ]
Cooper, Thomas A. [1 ]
机构
[1] Baylor Coll Med, Dept Pathol & Immunol, Houston, TX 77030 USA
[2] Baylor Coll Med, Interdept Program Cell & Mol Biol, Houston, TX 77030 USA
关键词
Microsatellite expansion; Neuromuscular disorder; RNA toxicity; RNA processing; RNA-binding protein; RNA foci; Alternative splicing; EXPANDED POLYGLUTAMINE PROTEIN; MYOTONIC-DYSTROPHY TYPE-1; FMR1; MESSENGER-RNA; ATAXIA TYPE 8; DROSOPHILA MODEL; CTG REPEATS; TRINUCLEOTIDE REPEAT; MUSCLEBLIND PROTEINS; HUNTINGTONS-DISEASE; INTRANUCLEAR INCLUSIONS;
D O I
10.1016/j.brainres.2012.02.030
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although protein-mediated toxicity in neurological disease has been extensively characterized, RNA-mediated toxicity is an emerging mechanism of pathogenesis. In microsatellite expansion disorders, expansion of repeated sequences in noncoding regions gives rise to RNA that produces a toxic gain of function, while expansions in coding regions can disrupt protein function as well as produce toxic RNA. The toxic RNA typically aggregates into nuclear foci and contributes to disease pathogenesis. In many cases, toxicity of the RNA is caused by the disrupted functions of RNA-binding proteins. We will discuss evidence for RNA-mediated toxicity in microsatellite expansion disorders. Different microsatellite expansion disorders are linked with alterations in the same as well as disease-specific RNA-binding proteins. Recent studies have shown that microsatellite expansions can encode multiple repeat-containing toxic RNAs through bidirectional transcription and protein species through repeat-associated non-ATG translation. We will discuss approaches that have characterized the toxic contributions of these various factors. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:100 / 111
页数:12
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