Rymond B C
Morgan School of Biological Sciences, University of Kentucky, Lexington 40506-0225.
SAAS Bull Biochem Biotechnol. 1991 Jan;4:76-80.
RNase H and synthetic DNA oligonucleotides were used to analyze the ribonucleoprotein (RNP) structure of the yeast spliceosome and to assay the pre-mRNA sequence requirements for step 1 of splicing. The data suggest that tight, stable contacts between the pre-mRNA and the spliceosome may be limited to the 5' splice site and branch point regions of the intron. A 30 nucleotide segment 3' of the branch point was found to be necessary for spliceosome maturation and essential for step 1 of splicing. Somewhat surprisingly, the 3' splice site was sensitive to nuclease digestion and completely dispensable for step 1 of splicing.
核糖核酸酶H和合成的DNA寡核苷酸被用于分析酵母剪接体的核糖核蛋白(RNP)结构,并检测剪接第一步对前体mRNA序列的要求。数据表明,前体mRNA与剪接体之间紧密、稳定的接触可能仅限于内含子的5'剪接位点和分支点区域。发现分支点下游30个核苷酸的片段对于剪接体成熟是必需的,并且对剪接第一步至关重要。有点令人惊讶的是,3'剪接位点对核酸酶消化敏感,并且对于剪接第一步是完全可有可无的。