Intronic CA-repeat and CA-rich elements:: a new class of regulators of mammalian alternative splicing

被引:179
作者
Hui, JY
Hung, LH
Heiner, M
Schreiner, S
Neumüller, N
Reither, G
Haas, SA
Bindereif, A
机构
[1] Univ Giessen, Fachbereich Biol, Inst Biochem, D-35392 Giessen, Germany
[2] Max Planck Inst Mol Genet, Dept Computat Mol Biol, Berlin, Germany
关键词
alternative splicing; hnRNP L; repetitive sequence; splicing enhancer; splicing silencer;
D O I
10.1038/sj.emboj.7600677
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
We have recently identified an intronic polymorphic CA-repeat region in the human endothelial nitric oxide synthase ( eNOS) gene as an important determinant of the splicing efficiency, requiring specific binding of hnRNP L. Here, we analyzed the position requirements of this CA-repeat element, which revealed its potential role in alternative splicing. In addition, we defined the RNA binding specificity of hnRNP L by SELEX: not only regular CA repeats are recognized with high affinity but also certain CA-rich clusters. Therefore, we have systematically searched the human genome databases for CA-repeat and CA-rich elements associated with alternative 5' splice sites (5'ss), followed by minigene transfection assays. Surprisingly, in several specific human genes that we tested, intronic CA RNA elements could function either as splicing enhancers or silencers, depending on their proximity to the alternative 5'ss. HnRNP L was detected specifically bound to these diverse CA elements. These data demonstrated that intronic CA sequences constitute novel and widespread regulatory elements of alternative splicing.
引用
收藏
页码:1988 / 1998
页数:11
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