Pre-mRNA splicing in disease and therapeutics

被引:327
作者
Singh, Ravi K. [1 ]
Cooper, Thomas A. [1 ,2 ,3 ]
机构
[1] Baylor Coll Med, Dept Pathol & Immunol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol Physiol & Biophys, Houston, TX 77030 USA
关键词
alternative splicing; cis mutations; trans splicing factors; spliceosome; splicing related human diseases; antisense oligonucleotide therapy; DUCHENNE MUSCULAR-DYSTROPHY; MYOTONIC-DYSTROPHY; DEVELOPMENTAL DISORDER; HEXANUCLEOTIDE REPEAT; CHLORIDE CHANNEL; PYRUVATE-KINASE; TRANSGENIC MICE; SKELETAL-MUSCLE; CANDIDATE-GENE; TOXIC RNA;
D O I
10.1016/j.molmed.2012.06.006
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
In metazoans, alternative splicing of genes is essential for regulating gene expression and contributing to functional complexity. Computational predictions, comparative genomics, and transcriptome profiling of normal and diseased tissues indicate that an unexpectedly high fraction of diseases are caused by mutations that alter splicing. Mutations in cis elements cause missplicing of genes that alter gene function and contribute to disease pathology. Mutations of core spliceosomal factors are associated with hematolymphoid neoplasias, retinitis pigmentosa, and microcephalic osteodysplastic primordial dwarfism type 1 (MOPD1). Mutations in the trans regulatory factors that control alternative splicing are associated with autism spectrum disorder, amyotrophic lateral sclerosis (ALS), and various cancers. In addition to discussing the disorders caused by these mutations, this review summarizes therapeutic approaches that have emerged to correct splicing of individual genes or target the splicing machinery.
引用
收藏
页码:472 / 482
页数:11
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