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U11小核RNA在体内与依赖U12的(AU-AC)前体信使核糖核酸内含子的5'剪接位点相互作用。

U11 snRNA interacts in vivo with the 5' splice site of U12-dependent (AU-AC) pre-mRNA introns.

作者信息

Kolossova I, Padgett R A

机构信息

Department of Molecular Biology, The Cleveland Clinic Foundation, Ohio 44195, USA.

出版信息

RNA. 1997 Mar;3(3):227-33.

Abstract

A notable feature of the newly described U12 snRNA-dependent class of eukaryotic nuclear pre-mRNA introns is the highly conserved 8-nt 5' splice site sequence. This sequence is virtually invariant in all known members of this class from plants to mammals. Based on sequence complementarity between this sequence and the 5' end of the U11 snRNA, we proposed that U11 snRNP may play a role in identifying and/or activating the 5' splice site for splicing. Here we show that mutations of the conserved 5' splice site sequence of a U12-dependent intron severely reduce correct splicing in vivo and that compensatory mutations in U11 snRNA can suppress the effects of the 5' splice site mutations to varying extents. This provides evidence for a required interaction between U11 snRNA and the 5' splice site sequence involving Watson-Crick base pairing. This data, in addition to a report that U11 snRNP is bound transiently to the U12-dependent spliceosome, suggests that U11 snRNP is the analogue of U1 snRNP in splicing this rare class of introns.

摘要

新描述的依赖U12 snRNA的真核细胞核前体mRNA内含子的一个显著特征是高度保守的8个核苷酸的5'剪接位点序列。该序列在从植物到哺乳动物的这类已知所有成员中几乎是不变的。基于该序列与U11 snRNA 5'端之间的序列互补性,我们提出U11 snRNP可能在识别和/或激活用于剪接的5'剪接位点中发挥作用。在此我们表明,U12依赖内含子保守的5'剪接位点序列的突变在体内严重降低了正确剪接,并且U11 snRNA中的补偿性突变可以不同程度地抑制5'剪接位点突变的影响。这为U11 snRNA与涉及沃森-克里克碱基配对的5'剪接位点序列之间的必需相互作用提供了证据。该数据,除了一份关于U11 snRNP与依赖U12的剪接体瞬时结合的报告之外,表明U11 snRNP在剪接这类罕见内含子时是U1 snRNP的类似物。

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