Cheng S C
Institute of Molecular Biology, Academia Sinica, Nankang, Taiwan, ROC.
Nucleic Acids Res. 1994 May 11;22(9):1548-54. doi: 10.1093/nar/22.9.1548.
Assembly of the spliceosome is a step-wise process and involves sequential binding of snRNAs to the pre-mRNA to form pre-splicing complex A2-1. Subsequent dissociation of U4 from the spliceosome is accompanied by formation of complex A1 (Genes Dev. 1, 1014-1027, 1987). We show that the 3' region of the intron sequence is not required for efficient assembly of the yeast spliceosome. Truncated precursor mRNA retaining only four or five nucleotides 3' to the TACTAAC box formed pre-splicing complex A1, kinetically the last pre-mRNA containing splicing complex identified. The subsequent cleavage--ligation reaction requires at least 23 nucleotides on the 3' side of the TACTAAC box in a sequence-independent manner. Immunoprecipitation with anti-PRP19 antibody showed that association of PRP19 with the spliceosome was also independent of the 3' region of the intron.
剪接体的组装是一个逐步的过程,涉及snRNA与前体mRNA的顺序结合以形成剪接前复合体A2-1。随后U4从剪接体上解离,同时形成复合体A1(《基因与发育》1, 1014 - 1027, 1987年)。我们发现,酵母剪接体的有效组装不需要内含子序列的3'区域。仅在TACTAAC框3'端保留四个或五个核苷酸的截短前体mRNA形成了剪接前复合体A1,从动力学角度来看,这是最后一个被鉴定出的含剪接复合体的前体mRNA。随后的切割-连接反应以序列无关的方式在TACTAAC框3'侧至少需要23个核苷酸。用抗PRP19抗体进行免疫沉淀表明,PRP19与剪接体的结合也与内含子的3'区域无关。