Ruskin B, Zamore P D, Green M R
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.
Cell. 1988 Jan 29;52(2):207-19. doi: 10.1016/0092-8674(88)90509-0.
Pre-mRNA splicing complex assembly is mediated by two specific pre-mRNA-snRNP interactions: U1 snRNP binds to the 5' splice site and U2 snRNP binds to the branch point. Here we show that unlike a purified U1 snRNP, which can bind to a 5' splice site, a partially purified U2 snRNP cannot interact with its target pre-mRNA sequence. We identify a previously uncharacterized activity, U2AF, that is required for the U2 snRNP-branch point interaction and splicing complex formation. Using RNA substrate exclusion and competition assays, we demonstrate that U2AF binds to the 3' splice site region prior to the U2 snRNP-branch point interaction. This provides an explanation for the necessity of the 3' splice site region in U2 snRNP binding and, hence, the first step of splicing.
前体mRNA剪接复合体的组装由两种特定的前体mRNA与snRNP的相互作用介导:U1 snRNP结合到5'剪接位点,U2 snRNP结合到分支点。我们在此表明,与能够结合到5'剪接位点的纯化U1 snRNP不同,部分纯化的U2 snRNP不能与其靶前体mRNA序列相互作用。我们鉴定出一种以前未被表征的活性,即U2辅助因子(U2AF),它是U2 snRNP与分支点相互作用以及剪接复合体形成所必需的。通过RNA底物排除和竞争试验,我们证明U2AF在U2 snRNP与分支点相互作用之前结合到3'剪接位点区域。这就解释了3'剪接位点区域在U2 snRNP结合中的必要性,从而也解释了剪接的第一步。