Wu S, Green M R
Howard Hughes Medical Institute, Program in Molecular Medicine, University of Massachusetts Medical Center, Worcester 01605, USA.
EMBO J. 1997 Jul 16;16(14):4421-32. doi: 10.1093/emboj/16.14.4421.
Accurate splicing of precursor mRNAs (pre-mRNAs) requires recognition of the 5' and 3' splice sites at the intron boundaries. Interactions between several splicing factors and the 5' splice site, which occur prior to the first step of splicing, have been well described. In contrast, recognition of the 3' splice site, which is cleaved during the second catalytic step, is poorly understood, particularly in higher eukaryotes. Here, using site-specific photo-crosslinking, we find that the conserved AG dinucleotide at the 3' splice site is contacted specifically by a 70 kDa polypeptide (p70). The p70-3' splice site crosslink has kinetics and biochemical requirements similar to those of splicing, was detected only in the mature spliceosome and occurs subsequent to the first step. Thus, p70 has all the properties expected of a factor that functionally interacts with the 3' splice site during the second step of splicing. Using antisera to various known splicing factors, we find that p70 corresponds to a previously reported 69 kDa protein of unknown function associated with the Sm core domain of spliceosomal small nuclear ribonucleoproteins.
前体mRNA(pre-mRNA)的准确剪接需要识别内含子边界处的5'和3'剪接位点。在剪接第一步之前,几种剪接因子与5'剪接位点之间的相互作用已得到充分描述。相比之下,在第二步催化过程中被切割的3'剪接位点的识别却了解甚少,尤其是在高等真核生物中。在此,我们利用位点特异性光交联技术发现,3'剪接位点处保守的AG二核苷酸与一种70 kDa的多肽(p70)发生特异性接触。p70与3'剪接位点的交联具有与剪接相似的动力学和生化要求,仅在成熟剪接体中检测到,且发生在第一步之后。因此,p70具有在剪接第二步与3'剪接位点发生功能相互作用的因子所预期的所有特性。使用针对各种已知剪接因子的抗血清,我们发现p70对应于先前报道的一种与剪接体小核核糖核蛋白的Sm核心结构域相关的、功能未知的69 kDa蛋白质。