Yang V W, Lerner M R, Steitz J A, Flint S J
Proc Natl Acad Sci U S A. 1981 Mar;78(3):1371-5. doi: 10.1073/pnas.78.3.1371.
The size and structure of viral RNA species synthesized in nuclei isolated during the early phase of productive infection by adenovirus type 2 have been examined by electrophoresis in denaturing polyacrylamide cells and the nuclease S1 assay. The major products of transcription in vitro of early regions 1 and 2 in the adenoviral genome are processed RNA molecules that appear to be correctly spliced in isolated nuclei. Splicing of adenoviral RNA molecules is inhibited when nuclei are preincubated with antibodies from systemic lupus erythematosus patients that immunoprecipitate small nuclear ribonucleoprotein particles. The specificity of these antibodies suggests that ribonucleoprotein particles containing U1 RNA are required for splicing of the adenoviral RNA sequences we have examined.
利用变性聚丙烯酰胺凝胶电泳和核酸酶S1测定法,对在腺病毒2型生产性感染早期分离的细胞核中合成的病毒RNA种类的大小和结构进行了检测。腺病毒基因组中早期区域1和2在体外转录的主要产物是经过加工的RNA分子,这些分子似乎在分离的细胞核中被正确剪接。当细胞核与来自系统性红斑狼疮患者的抗体进行预孵育时,腺病毒RNA分子的剪接受到抑制,这些抗体能免疫沉淀小核核糖核蛋白颗粒。这些抗体的特异性表明,我们所检测的腺病毒RNA序列的剪接需要含有U1 RNA的核糖核蛋白颗粒。