Wu G J
Proc Natl Acad Sci U S A. 1978 May;75(5):2175-9. doi: 10.1073/pnas.75.5.2175.
A cell-free system developed from human KB cells was used to transcribe 5.5S RNA from deproteinized adenovirus DNA in vitro. The cell-free RNA synthesis is dependent upon exogenous templates, ribonucleoside triphosphates, and cell-free postmitochondrial supernatant of human KB cells. The synthesis of 5.5S RNA is inhibited only by high levels of alpha-amanitin; therefore it is carried out by RNA polymerase III. The rate of synthesis was linear for at least 2 hr, indicating reinitiation. The 5.5S RNA synthesized in vitro is similar to the corresponding in vivo RNA in size, sequence, and coding region on adenovirus type 2 DNA. In this report is demonstrated in vitro synthesis of a facsimile of an in vivo transcript directed by deproteinized DNA in a mammalian cell-free postmitochondrial supernatant system.
一个由人KB细胞构建的无细胞系统被用于在体外从脱蛋白的腺病毒DNA转录5.5S RNA。无细胞RNA合成依赖于外源模板、核糖核苷三磷酸以及人KB细胞的无细胞线粒体后上清液。5.5S RNA的合成仅被高水平的α-鹅膏蕈碱抑制;因此它是由RNA聚合酶III进行的。合成速率至少在2小时内呈线性,表明存在重新起始。体外合成的5.5S RNA在大小、序列以及腺病毒2型DNA上的编码区域方面与相应的体内RNA相似。本报告展示了在哺乳动物无细胞线粒体后上清液系统中由脱蛋白DNA指导的体内转录本的体外模拟合成。