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使用特定放射性探针研究流感病毒基因组的转录和复制。

Use of specific radioactive probes to study transcription and replication of the influenza virus genome.

作者信息

Taylor J M, Illmensee R, Litwin S, Herring L, Broni B, Krug R M

出版信息

J Virol. 1977 Feb;21(2):530-40. doi: 10.1128/JVI.21.2.530-540.1977.

Abstract

Specific radioactive probes have been obtained for both influenza virion RNA (vRNA) and for its complement (complementary RNA or cRNA): 32P-labeled complementary DNA (cDNA) synthesized with the avian sarcoma virus reverse transcriptase, and [125I]vRNA, respectively. From the kinetics of annealing of these two probes to RNA from canine kidney cells infected with the WSN strain of influenza virus, we have determined the average number of cRNA and vRNA sequences in the nucleus and cytoplasm as a function of time after infection. Immediately after infection, a small amount of vRNA is detected, presumably from the inoculum virus. As expected, the amount of cRNA is insignificant. During the first 1.75 h of infection, the most significant increase observed is in cRNA sequences. Most of these cRNA sequences are found in the cytoplasm, but a significant amount (30%) is found in the nucleus. During this time, a small but significant increase in vRNA is also detected in the nucleus and cytoplasm. From 1.75 to 2.75 h, the absolute amounts of both cRNA and vRNA increase, predominantly in the cytoplasm, with cRNA remaining as the majority species. Subsequently, the amount of vRNA increases with respect to cRNA and becomes the majority species. At 3.75 h, 95% of both cRNA and vRNA are found in the cytoplasm. Addition of actinomycin D at 1.75 h completely suppresses the subsequent ninefold increase in cRNA and does not have a significant effect on the subsequent 14-fold increase in cytoplasmic vRNA. This assay is also able to detect the cRNA produced as a result of primary transcription, operationally defined as the cRNA produced in the presence of 100 mug of cycloheximide per ml added at zero time of infection. Increases in cRNA in the presence of cycloheximide are detectable in both the nucleus and the cytoplasm. Addition of actinomycin D as well as cycloheximide at zero time completely suppresses the appearance of cRNA in the cytoplasm, whereas a large fraction (50%) of the increase in nuclear cRNA still occurs.

摘要

已经获得了针对流感病毒粒子RNA(vRNA)及其互补物(互补RNA或cRNA)的特异性放射性探针:分别是用禽肉瘤病毒逆转录酶合成的32P标记的互补DNA(cDNA)和[125I]vRNA。根据这两种探针与感染了流感病毒WSN株的犬肾细胞RNA退火的动力学,我们确定了感染后不同时间细胞核和细胞质中cRNA和vRNA序列的平均数量。感染后立即检测到少量vRNA,推测来自接种病毒。正如预期的那样,cRNA的量微不足道。在感染的最初1.75小时内,观察到的最显著增加是cRNA序列。这些cRNA序列大多存在于细胞质中,但相当数量(30%)存在于细胞核中。在此期间,细胞核和细胞质中的vRNA也有少量但显著的增加。从1.75小时到2.75小时,cRNA和vRNA的绝对量都增加,主要在细胞质中,cRNA仍然是主要种类。随后,vRNA相对于cRNA增加并成为主要种类。在3.75小时时,95%的cRNA和vRNA都存在于细胞质中。在1.75小时添加放线菌素D完全抑制了随后cRNA九倍的增加,并且对随后细胞质中vRNA十四倍的增加没有显著影响。该测定法还能够检测到初级转录产生的cRNA,在操作上定义为在感染零时每毫升添加100微克环己酰亚胺的情况下产生的cRNA。在细胞核和细胞质中都可检测到在环己酰亚胺存在下cRNA的增加。在零时添加放线菌素D以及环己酰亚胺完全抑制了细胞质中cRNA的出现,而细胞核中cRNA增加的很大一部分(50%)仍然会发生。

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