CUG-BP, Elav-like family (CELF)-mediated alternative splicing regulation in the brain during health and disease

被引:50
作者
Ladd, Andrea N. [1 ]
机构
[1] Cleveland Clin, Lerner Res Inst, Dept Cellular & Mol Med, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
Alternative splicing; CUG-BP; Elav-like family; Brain; Neurons; Neurological disorders; Myotonic dystrophy; RNA-BINDING PROTEIN; MYOTONIC-DYSTROPHY TYPE-1; PRE-MESSENGER-RNA; NERVOUS-SYSTEM; TRIPLET REPEAT; NUCLEAR FOCI; MUSCLEBLIND PROTEINS; EXPRESSION PATTERNS; GENE-EXPRESSION; CELF FAMILY;
D O I
10.1016/j.mcn.2012.12.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alternative splicing is an important mechanism for generating transcript and protein diversity. In the brain, alternative splicing is particularly prevalent, and alternative splicing factors are highly enriched. These include the six members of the CUG-BP, Elav-like family (CELF). This review summarizes what is known about the expression of different CELF. proteins in the nervous system and the evidence that they are important in neural development and function. The involvement of CELF proteins in the pathogenesis of a number of neurodegenerative disorders, including myotonic dystrophy, spinocerebellar ataxia, fragile X syndrome, spinal muscular atrophy, and spinal and bulbar muscular atrophy is discussed. Finally, the known targets of CELF-mediated alternative splicing regulation in the nervous system and the functional consequences of these splicing events are reviewed. This article is part of a Special Issue entitled "RNA and splicing regulation in neurodegeneration." (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:456 / 464
页数:9
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