A downstream splicing enhancer is essential for in vitro pre-mRNA splicing

被引:9
作者
Yue, BG [1 ]
Akusjärvi, G [1 ]
机构
[1] Univ Uppsala, BMC, Dept Med Biochem & Microbiol, S-75123 Uppsala, Sweden
关键词
RNA splicing; Ul snRNP; SR protein; splicing enhancer; adenovirus L1;
D O I
10.1016/S0014-5793(99)00521-9
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
Splicing enhancers have previously been shown to promote processing of introns containing weak splicing signals. Here, me extend these studies by showing that also 'strong' constitutively active introns are absolutely dependent on a downstream splicing enhancer for activity in vitro. SR protein binding to exonic enhancer elements or U1 snRNP binding to a downstream 5' splice site serve redundant functions as activators of splicing. We further show that a 5' splice site is most effective as an enhancer of splicing. Thus, a 5' splice site is functional in S100 extracts, under conditions where a SR enhancer is nonfunctional. Also, splice site pairing occurs efficiently in the absence of exonic SR enhancers, emphasizing the significance of a downstream 5' splice site as the enhancer element in vertebrate splicing. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:10 / 14
页数:5
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