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放线菌酮对腺病毒2 productive感染早期RNA代谢的影响

Effect of cycloheximide on RNA metabolism early in productive infection with adenovirus 2.

作者信息

Craig E A, Raskas H J

出版信息

J Virol. 1974 Jul;14(1):26-32. doi: 10.1128/JVI.14.1.26-32.1974.

Abstract

The presence of cycloheximide during the early phase of adenovirus 2 replication causes an increase in the virus-specific content of newly synthesized mRNA. The total cytoplasmic RNA from control cultures labeled 2 to 5 h after infection hybridized to viral DNA 0.8%, whereas RNA synthesized in the presence of cycloheximide annealed 6%. Cytosine arabinoside, an inhibitor of DNA synthesis, did not affect the percent hybridization to viral DNA. Oligo(dT)-cellulose chromatography was used to purify the portion of cytoplasmic RNA containing poly(A). The poly(A)-containing RNA from cultures labeled in the presence of cycloheximide hybridized to viral DNA 32% as compared to 2.2% for RNA from control cultures. Hybridization-inhibition experiments between RNAs from control- and cycloheximide-treated cultures demonstrated that the cultures treated with cycloheximide did not have an increased content of viral RNA or a new class of viral RNA sequences. Therefore, the increased hybridization appears to be caused by a reduction in synthesis of cellular cytoplasmic mRNA. Nucleoplasmic RNAs lacking and containing poly(A) were annealed to viral DNA. For both classes, RNA from cultures treated with cycloheximide hybridized 5- to 10-fold more than RNA from control-infected cultures. Therefore, the increased hybridization of cytoplasmic RNA synthesized in the presence of cycloheximide is caused either by reduced transcription of the cellular genome or by greatly increased instability of cellular heterogeneous nuclear RNA.

摘要

在腺病毒2复制早期阶段存在放线菌酮会导致新合成的mRNA中病毒特异性含量增加。感染后2至5小时标记的对照培养物的总细胞质RNA与病毒DNA的杂交率为0.8%,而在放线菌酮存在下合成的RNA退火率为6%。阿糖胞苷是一种DNA合成抑制剂,不影响与病毒DNA的杂交百分比。使用寡聚(dT)-纤维素色谱法纯化细胞质RNA中含聚(A)的部分。与对照培养物的RNA的2.2%相比,在放线菌酮存在下标记的培养物中含聚(A)的RNA与病毒DNA的杂交率为32%。对照培养物和放线菌酮处理培养物的RNA之间的杂交抑制实验表明,用放线菌酮处理的培养物中病毒RNA含量没有增加,也没有新的一类病毒RNA序列。因此,杂交增加似乎是由细胞细胞质mRNA合成减少引起的。将缺乏和含有聚(A)的核质RNA与病毒DNA退火。对于这两类,用放线菌酮处理的培养物的RNA杂交率比对照感染培养物的RNA高5至10倍。因此,在放线菌酮存在下合成的细胞质RNA杂交增加是由细胞基因组转录减少或细胞异质核RNA的不稳定性大大增加引起的。

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