Rymond B C, Rosbash M
Biology Department, Brandeis University, Waltham, Massachusetts 02254.
Genes Dev. 1988 Apr;2(4):428-39. doi: 10.1101/gad.2.4.428.
A chemical modification/interference assay was used to determine the yeast pre-mRNA sequence requirements for in vitro spliceosome assembly and splicing. Modifications of any of the nucleotides within the 5' splice site and branch point (TACTAAC box) consensus sequences as well as less conserved intron and exon positions were found to inhibit assembly and/or splicing. The interference pattern of the 5' splice site and TACTAAC box lesions increased as spliceosome assembly proceeded (complex III----complex I----complex II) and as splicing proceeded, suggesting that these sequence elements play multiple roles in the assembly of yeast spliceosomes and in the removal of intervening sequences. Furthermore, modification (or mutation) of a TACTAAC-like sequence upstream of the branch point was found to inhibit the rate of spliceosome assembly, implying a possible role for degenerate branch point sequences in modulating the efficiency of spliceosome assembly.
采用化学修饰/干扰试验来确定酵母前体mRNA序列对于体外剪接体组装和剪接的要求。发现5'剪接位点和分支点(TACTAAC框)共有序列内的任何核苷酸以及保守性较低的内含子和外显子位置发生修饰时,均会抑制组装和/或剪接。随着剪接体组装的进行(复合体III→复合体I→复合体II)以及剪接的进行,5'剪接位点和TACTAAC框损伤的干扰模式增强,这表明这些序列元件在酵母剪接体的组装以及间隔序列的去除过程中发挥多种作用。此外,发现分支点上游类似TACTAAC的序列发生修饰(或突变)会抑制剪接体组装速率,这意味着简并分支点序列在调节剪接体组装效率方面可能发挥作用。