Orellana T, Kieff E
J Virol. 1977 May;22(2):321-30. doi: 10.1128/JVI.22.2.321-330.1977.
The complexity and abundance of Epstein-Barr (EBV)-specific RNA in cell cultures restringently, abortively, and productively infected with EBV has been analyed by hybridization of the infected cell RNA with purified viral DNA. The data indicate the following. (i) Cultures containing productively infected cells contain viral RNA encoded by at least 45% of EBV DNA, and almost all of the species of viral RNA are present in the polyadenylated and polyribosomal RNA fractions. (ii) Restringently infected Namalwa and Raji cultures, which contain only intranuclear antigen, EBNA, and enhanced capacity for growth in vitro, contain EBV RNA encoded by at least 16 and 30% of the EBV DNA, respectively. The polyadenylated and polyribosomal RNA fractions of Raji and Namalwa cells are enriched for a class of EBV RNA encoded by approximately 5% of EBV DNA. The same EBV DNA sequences encode the polyadenylated and polyribosomal RNA of both Raji and Namalwa cells. (iii) After superinfection of Raji cultures with EBV (HR-1), the abortively infected cells contain RNA encoded by at least 41% of EBV DNA. The polyadenylated RNA of superinfected Raji cells is enriched for a class of EBV RNA encoded by approximately 20% of EBV HR-1 DNA. Summation hybridization experiments suggest that the polyadenylated RNA in superinfected Raji cells is encoded by the same DNA sequences as encode RNA present in Raji cells before superinfection, most of which is not polyadenylated. That the same EBV RNA sequences are present in the polyadenylated and polyribosomal fractions of two independently derived, restringently infected cell lines suggests that these RNAs may specify functions related to maintenance of the transformed state. The complexity of this class of RNA is adequate to specify a sequence of a least 5,000 amino acids. That only some RNA species are polyadenylated in restringent and abortive infection suggests that polyadenylation or whatever determines polyadenylation may play a role in the restricted expression of the EVB genome.
通过将感染细胞的RNA与纯化的病毒DNA进行杂交,对在严格、流产和生产性感染爱泼斯坦-巴尔病毒(EBV)的细胞培养物中EBV特异性RNA的复杂性和丰度进行了分析。数据表明如下情况。(i)含有生产性感染细胞的培养物中含有由至少45%的EBV DNA编码的病毒RNA,并且几乎所有种类的病毒RNA都存在于聚腺苷酸化和多核糖体RNA组分中。(ii)严格感染的Namalwa和Raji培养物,仅含有核内抗原EBNA,且体外生长能力增强,分别含有由至少16%和30%的EBV DNA编码的EBV RNA。Raji和Namalwa细胞的聚腺苷酸化和多核糖体RNA组分富含一类由约5%的EBV DNA编码的EBV RNA。相同的EBV DNA序列编码Raji和Namalwa细胞的聚腺苷酸化和多核糖体RNA。(iii)用EBV(HR - 1)对Raji培养物进行超感染后,流产感染的细胞含有由至少41%的EBV DNA编码的RNA。超感染的Raji细胞的聚腺苷酸化RNA富含一类由约20%的EBV HR - 1 DNA编码的EBV RNA。总和杂交实验表明,超感染的Raji细胞中的聚腺苷酸化RNA由与超感染前Raji细胞中存在的RNA相同的DNA序列编码,其中大部分不是聚腺苷酸化的。在两个独立衍生的、严格感染的细胞系的聚腺苷酸化和多核糖体组分中存在相同的EBV RNA序列,这表明这些RNA可能指定与维持转化状态相关的功能。这类RNA的复杂性足以指定至少5000个氨基酸的序列。在严格和流产感染中只有一些RNA种类是聚腺苷酸化的,这表明聚腺苷酸化或任何决定聚腺苷酸化的因素可能在EBV基因组的受限表达中起作用。