Bodemer W, Knust E, Angermüller S, Fleckenstein B
J Virol. 1984 Aug;51(2):452-7. doi: 10.1128/JVI.51.2.452-457.1984.
Transcription of Herpesvirus saimiri was characterized during the initial phases of productive infection by Northern blot analyses and hybridizations of radioactive cDNA with cloned fragments of virion L-DNA. Under conditions of immediate-early transcription, e.g., blocking of viral protein synthesis by cycloheximide, a single cytoplasmic polyadenylated viral RNA of 2.7 kilobases was found in infected cells. The sequence coding for this RNA was between map units 0.89 and 0.93; it was transcribed from right to left in prototype arrangement of M-DNA. The immediate-early mRNA of lytically infected cells appeared to be very similar, if not identical, to the single viral RNA species found in lymphoid cells transformed by H. saimiri.
通过Northern印迹分析以及放射性cDNA与病毒粒子L-DNA克隆片段的杂交,对赛米利疱疹病毒在增殖性感染初始阶段的转录进行了表征。在立即早期转录的条件下,例如用放线菌酮阻断病毒蛋白合成,在感染细胞中发现了一种2.7千碱基的单一细胞质多聚腺苷酸化病毒RNA。编码该RNA的序列位于图谱单位0.89和0.93之间;它在M-DNA的原型排列中从右向左转录。裂解感染细胞的立即早期mRNA似乎与在被赛米利疱疹病毒转化的淋巴细胞中发现的单一病毒RNA种类非常相似,甚至相同。