Madhani H D, Guthrie C
Department of Biochemistry and Biophysics, University of California, San Francisco 94143.
Cell. 1992 Nov 27;71(5):803-17. doi: 10.1016/0092-8674(92)90556-r.
Prior to the chemical steps of mRNA splicing, the extensive base-pairing interaction between the U4 and U6 spliceosomal snRNAs is disrupted. Here, we use a mutational analysis in yeast to demonstrate a conserved base-pairing interaction between the U6 and U2 snRNAs that is mutually exclusive with the U4-U6 interaction. In this novel pairing, conserved sequences in U6 interact with a sequence in U2 that is immediately upstream of the branch point recognition region. Remarkably, the residues in U6 that can be consequently juxtaposed with the intron substrate include those that have been proposed previously to be catalytic. Both the first and second steps of splicing are inhibited when this base-paired structure is mutated. These observations, together with the high conservation of the U2-U6 structure, lead us to propose that it might be a component of the spliceosomal active site.
在mRNA剪接的化学步骤之前,U4和U6剪接体snRNA之间广泛的碱基配对相互作用被破坏。在这里,我们利用酵母中的突变分析来证明U6和U2 snRNA之间保守的碱基配对相互作用,该相互作用与U4-U6相互作用相互排斥。在这种新的配对中,U6中的保守序列与U2中位于分支点识别区域上游紧邻的序列相互作用。值得注意的是,U6中随后可与内含子底物并列的残基包括先前被认为具有催化作用的残基。当这种碱基配对结构发生突变时,剪接的第一步和第二步均受到抑制。这些观察结果,连同U2-U6结构的高度保守性,使我们提出它可能是剪接体活性位点的一个组成部分。