Parker R, Siliciano P G
Department of Molecular and Cellular Biology, University of Arizona, Tucson 85721.
Nature. 1993 Feb 18;361(6413):660-2. doi: 10.1038/361660a0.
Nuclear pre-messenger RNA splicing requires the action of five small nuclear (sn) RNAs, U1, U2, U4, U5 and U6, and more than 50 proteins. The mechanistic similarity of nuclear pre-mRNA splicing and group II self-splicing suggests that many of the central processes of nuclear pre-mRNA splicing are based on RNA-RNA interaction. To understand the mechanism of pre-mRNA splicing, the interactions, and their temporal relationships, that occur between the snRNAs and the pre-mRNA during splicing must be identified. Several snRNA-snRNA and snRNA-intron interactions have been demonstrated but the putative RNA-based interactions that recognize the AG dinucleotide at the 3' splice site during 3' cleavage and exon ligation are unknown. We report here the reciprocal suppression between 5' and 3' splice site mutations in the yeast actin intron, and propose that the 3' splice site is positioned for 3' cleavage and exon ligation, at least in part, through a non-Watson-Crick interaction between the guanosines at the 5' and 3' splice sites.
细胞核前体信使核糖核酸(pre-mRNA)剪接需要5种小核(sn)RNA(U1、U2、U4、U5和U6)以及50多种蛋白质的作用。细胞核前体mRNA剪接与II类自剪接在机制上的相似性表明,细胞核前体mRNA剪接的许多核心过程都基于RNA-RNA相互作用。为了理解前体mRNA剪接的机制,必须确定剪接过程中snRNA与前体mRNA之间发生的相互作用及其时间关系。已经证实了几种snRNA-snRNA和snRNA-内含子相互作用,但在3'切割和外显子连接过程中识别3'剪接位点处AG二核苷酸的假定基于RNA的相互作用尚不清楚。我们在此报告酵母肌动蛋白内含子中5'和3'剪接位点突变之间的相互抑制作用,并提出3'剪接位点至少部分是通过5'和3'剪接位点处鸟苷之间的非沃森-克里克相互作用来定位进行3'切割和外显子连接的。