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干扰素对单链和双链脑心肌炎病毒核糖核酸聚合作用的影响。

Effect of interferon on polymerization of single-stranded and double-stranded mengovirus ribonucleic acid.

作者信息

Gordon I, Chenault S S, Stevenson D, Acton J D

出版信息

J Bacteriol. 1966 Mar;91(3):1230-8. doi: 10.1128/jb.91.3.1230-1238.1966.

Abstract

Gordon, Irving (University of Southern California, Los Angeles), Sara S. Chenault, Douglas Stevenson, and Jean D. Acton. Effect of interferon on polymerization of single-stranded and double-stranded mengovirus ribonucleic acid. J. Bacteriol. 91:1230-1238. 1966.-The effect of interferon on actinomycin-resistant mengovirus ribonucleic acid (RNA) replication in L cells was investigated to determine whether defective or partially polymerized RNA products were made and whether synthesis of any specific class of virus RNA was prevented. RNA labeled with uridine-C(14) was extracted in hot and cold phenol and analyzed by zonal sucrose density centrifugation. Both single- and double-stranded infectious RNA peaks were identified. Interferon treatment caused almost complete depression of uridine-C(14) incorporation throughout linear sucrose gradients except in the 4S region, and no infectivity was detectable in any fraction. These inhibitory effects are attributable to the action of interferon, because they were reversed when cultures were treated with actinomycin D simultaneously with interferon. The results, with those of other investigators, indicate that the step at which interferon interrupts virus multiplication is between the events immediately after uncoating and the formation of template "minus" strands; under the conditions of our experiments, no partially polymerized virus RNA products were made.

摘要

戈登,欧文(南加州大学,洛杉矶),萨拉·S·谢诺特,道格拉斯·史蒂文森,以及让·D·阿克顿。干扰素对单链和双链脑心肌炎病毒核糖核酸聚合的影响。《细菌学杂志》91:1230 - 1238。1966年。——研究了干扰素对L细胞中对放线菌素耐药的脑心肌炎病毒核糖核酸(RNA)复制的影响,以确定是否产生了有缺陷或部分聚合的RNA产物,以及是否阻止了任何特定类别的病毒RNA的合成。用尿苷 - C(14)标记的RNA在热酚和冷酚中提取,并通过区带蔗糖密度离心进行分析。鉴定出了单链和双链感染性RNA峰。干扰素处理导致整个线性蔗糖梯度中尿苷 - C(14)掺入几乎完全受到抑制,除了在4S区域,并且在任何组分中都检测不到感染性。这些抑制作用可归因于干扰素的作用,因为当培养物同时用放线菌素D和干扰素处理时,这些作用被逆转。这些结果与其他研究者的结果表明,干扰素中断病毒增殖的步骤是在脱壳后紧接着的事件与模板“负”链形成之间;在我们的实验条件下,没有产生部分聚合的病毒RNA产物。

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本文引用的文献

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THE CELLULAR SITES OF SYNTHESIS OF RIBOSOMAL AND 4S RNA.核糖体RNA和4S RNA的合成细胞位点。
Proc Natl Acad Sci U S A. 1962 Dec;48(12):2179-86. doi: 10.1073/pnas.48.12.2179.
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