Alternative splicing: A new drug target of the post-genome era

被引:72
作者
Hagiwara, M [1 ]
机构
[1] Tokyo Med & Dent Univ, Med Res Inst, Dept Funct Genom, Tokyo 1138510, Japan
[2] Tokyo Med & Dent Univ, Sch Biomed Sci, Gene Express Lab, Tokyo 1138510, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2005年 / 1754卷 / 1-2期
关键词
alternative splicing; SR protein; Clk; SRPK; TG003; SPINAL MUSCULAR-ATROPHY; PROTEIN-SPECIFIC KINASE; HETEROGENEOUS RIBONUCLEOPROTEIN A1; TOPOISOMERASE-I; SR PROTEINS; SERINE-RICH; DNA TOPOISOMERASE; SINGLE NUCLEOTIDE; CONSERVED FAMILY; FACTOR SF2/ASF;
D O I
10.1016/j.bbapap.2005.09.010
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
Alternative splicing allows for the creation of multiple distinct mRNA transcripts from a given gene in a multicellular organism. Pre-mRNA splicing is catalyzed by a multi-molecular complex, including serine/arginine-rich (SR) proteins, which are highly phosphorylated in living cells, and thought to play crucial roles in spliceosomal formation and in the regulation of alternative splicing. Recently, reports of low molecular compounds, which alter splicing pattern of genes, have been accumulated. A benzothiazole compound TG003, a kinase inhibitor that targets Clk1 and CIk4, suppressed dissociation of nuclear speckles, altered the splicing patterns, and rescued the embryonic defects induced by excessive Clk activity. The emerging inhibitors of the signal transduction pathways regulating pre-mRNA alternative splicing may open the way to therapies against diseases caused by missplicing. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:324 / 331
页数:8
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