Kennedy C F, Krämer A, Berget S M
Verna and Marrs McLean Department of Biochemistry, Program in Cell and Molecular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Mol Cell Biol. 1998 Sep;18(9):5425-34. doi: 10.1128/MCB.18.9.5425.
One of the earliest steps in pre-mRNA recognition involves binding of the splicing factor U2 snRNP auxiliary factor (U2AF or MUD2 in Saccharomyces cerevisiae) to the 3' splice site region. U2AF interacts with a number of other proteins, including members of the serine/arginine (SR) family of splicing factors as well as splicing factor 1 (SF1 or branch point bridging protein in S. cerevisiae), thereby participating in bridging either exons or introns. In vertebrates, the binding site for U2AF is the pyrimidine tract located between the branch point and 3' splice site. Many small introns, especially those in nonvertebrates, lack a classical 3' pyrimidine tract. Here we show that a 59-nucleotide Drosophila melanogaster intron contains C-rich pyrimidine tracts between the 5' splice site and branch point that are needed for maximal binding of both U1 snRNPs and U2 snRNPs to the 5' and 3' splice site, respectively, suggesting that the tracts are the binding site for an intron bridging factor. The tracts are shown to bind both U2AF and the SR protein SRp54 but not SF1. Addition of a strong 3' pyrimidine tract downstream of the branch point increases binding of SF1, but in this context, the upstream pyrimidine tracts are inhibitory. We suggest that U2AF- and/or SRp54-mediated intron bridging may be an alternative early recognition mode to SF1-directed bridging for small introns, suggesting gene-specific early spliceosome assembly.
前体mRNA识别的最早步骤之一涉及剪接因子U2 snRNP辅助因子(酿酒酵母中的U2AF或MUD2)与3'剪接位点区域的结合。U2AF与许多其他蛋白质相互作用,包括丝氨酸/精氨酸(SR)剪接因子家族的成员以及剪接因子1(SF1或酿酒酵母中的分支点桥接蛋白),从而参与连接外显子或内含子。在脊椎动物中,U2AF的结合位点是位于分支点和3'剪接位点之间的嘧啶序列。许多小内含子,尤其是非脊椎动物中的那些,缺乏经典的3'嘧啶序列。在这里,我们表明一个59个核苷酸的黑腹果蝇内含子在5'剪接位点和分支点之间含有富含C的嘧啶序列,这分别是U1 snRNP和U2 snRNP与5'和3'剪接位点最大结合所必需的,这表明这些序列是内含子桥接因子的结合位点。这些序列被证明能结合U2AF和SR蛋白SRp54,但不能结合SF1。在分支点下游添加一个强的3'嘧啶序列会增加SF1的结合,但在这种情况下,上游的嘧啶序列具有抑制作用。我们认为,对于小内含子,U2AF和/或SRp54介导的内含子桥接可能是SF1指导的桥接的一种替代早期识别模式,这表明存在基因特异性的早期剪接体组装。