Talley-Brown S, Millette R L
J Virol. 1979 Sep;31(3):733-40. doi: 10.1128/JVI.31.3.733-740.1979.
RNAs which are synthesized and accumulate in the cytoplasm of uninfected and herpes simplex virus type 1 (HSV-1)-infected xeroderma pigmentosum (XP) cells in the presence of cycloheximide (early RNAs) or absence of drugs (late RNAs) were analyzed by electrophoresis through denaturing polyacrylamide gradient slab gels. HSV RNAs were selected by hybridization ot HSV DNA covalently bound to cellulose. No HSV-specific low-molecular-weight (4S to 10S) RNAs were detected. However, several changes were observed in the electrophoretic pattern of the host low-molecular-weight RNAs during HSV infection. Five HSV RNAs ranging in size from 16S to 28S accumulated in the cytoplasm of infected XP cells in the presence of cycloheximide. These are of the size range predicted to encode the major early viral polypeptides. The cytoplasmic and polyadenylated early RNAs from HSV-infected XP cells were translated in vitro to produce proteins whose electrophoretic pattern resembled that of the early viral proteins synthesized in vivo.
在存在环己酰亚胺(早期RNA)或不存在药物(晚期RNA)的情况下,对在未感染和单纯疱疹病毒1型(HSV-1)感染的着色性干皮病(XP)细胞细胞质中合成并积累的RNA进行分析,通过变性聚丙烯酰胺梯度平板凝胶电泳进行。通过与共价结合到纤维素上的HSV DNA杂交来选择HSV RNA。未检测到HSV特异性低分子量(4S至10S)RNA。然而,在HSV感染期间,宿主低分子量RNA的电泳图谱观察到了一些变化。在存在环己酰亚胺的情况下,5种大小从16S到28S的HSV RNA在受感染的XP细胞细胞质中积累。这些处于预测编码主要早期病毒多肽的大小范围内。来自HSV感染的XP细胞的细胞质和多聚腺苷酸化早期RNA在体外进行翻译以产生蛋白质,其电泳图谱类似于体内合成的早期病毒蛋白的电泳图谱。