Wyatt J R, Sontheimer E J, Steitz J A
Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, Howard Hughes Medical Institute, Boyer Center for Molecular Medicine, New Haven, Connecticut 06536-0812.
Genes Dev. 1992 Dec;6(12B):2542-53. doi: 10.1101/gad.6.12b.2542.
We have used a site-specific cross-linking strategy to identify RNA and protein factors that interact with the 5' splice site region during mammalian pre-mRNA splicing. Two different pre-mRNA substrates were synthesized with a single 32P-labeled 4-thiouridine residue 2 nucleotides upstream of the 5' splice site. Selective photoactivation of the 4-thiouridine residue after incubation of either substrate under splicing conditions in HeLa nuclear extract resulted in cross-links to the U5 snRNA and the U5 snRNP protein p220. These ATP-dependent interactions occur before the first step of splicing. The U5 snRNA cross-links map to a phylogenetically invariant 9-nucleotide loop sequence and do not require Watson-Crick complementarity to the 5' exon. Cross-links of this position in the pre-mRNA to U1, but not to U2, U4, or U6 snRNAs, were also observed. The kinetics of U1 and U5 cross-link formation are similar, both peaking well before reaction intermediates appear.
我们采用了位点特异性交联策略,以鉴定在哺乳动物前体mRNA剪接过程中与5'剪接位点区域相互作用的RNA和蛋白质因子。在5'剪接位点上游2个核苷酸处有一个单一的32P标记的4-硫尿苷残基,以此合成了两种不同的前体mRNA底物。在HeLa细胞核提取物中于剪接条件下孵育任一底物后,对4-硫尿苷残基进行选择性光活化,结果导致其与U5 snRNA和U5 snRNP蛋白p220发生交联。这些依赖ATP的相互作用发生在剪接的第一步之前。U5 snRNA交联定位于系统发育上不变的9核苷酸环序列,并且不需要与5'外显子形成沃森-克里克互补配对。还观察到前体mRNA中该位置与U1 snRNA发生交联,但与U2、U4或U6 snRNA不发生交联。U1和U5交联形成的动力学相似,两者均在反应中间体出现之前达到峰值。