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苜蓿银纹夜蛾核型多角体病毒温度敏感突变体的分离:杆状病毒突变体在极晚期基因表达缺陷的表型特征分析

Isolation of temperature sensitive mutants of Autographa californica nuclear polyhedrosis virus: phenotype characterization of baculovirus mutants defective in very late gene expression.

作者信息

Partington S, Yu H, Lu A, Carstens E B

机构信息

Department of Microbiology & Immunology, Queen's University, Kingston, Ontario, Canada.

出版信息

Virology. 1990 Mar;175(1):91-102. doi: 10.1016/0042-6822(90)90189-x.

Abstract

Temperature sensitive mutants of Autographa californica nuclear polyhedrosis virus were isolated following exposure of parental replicating virus to 5-bromo-2'-deoxyuridine. Two mutants designated ts317 and ts538 were characterized in detail. Both mutants synthesized viral DNA but were defective in infectious extracellular virus production at the nonpermissive temperature suggesting defects in late gene regulation. Pulse-labeling experiments indicated that a switch to late protein synthesis occurred but this synthesis was not maintained with either mutant since all protein synthesis was gradually inhibited by 20 hr postinfection at 33 degrees. Western blots probed with antisera directed against either extracellular virus proteins or very late proteins showed a reduction in late structural proteins, a 10-fold reduction in polyhedrin, and an absence of p10 at the nonpermissive temperature. Northern blots of total intracellular RNA showed that specific late and very late transcripts were synthesized in greatly reduced amounts at the nonpermissive temperature suggesting the absence of very late proteins was a result of inhibition of virus-specific transcription. The genetic analyses indicate that the mutations lie in two closely linked genes, both important in regulating the induction of very late transcription and translation.

摘要

将亲本复制病毒暴露于5-溴-2'-脱氧尿苷后,分离出了苜蓿银纹夜蛾核型多角体病毒的温度敏感突变体。详细鉴定了两个命名为ts317和ts538的突变体。两个突变体均能合成病毒DNA,但在非允许温度下感染性细胞外病毒产生存在缺陷,提示晚期基因调控存在缺陷。脉冲标记实验表明发生了向晚期蛋白质合成的转换,但由于在33℃感染后20小时所有蛋白质合成均逐渐受到抑制,这两种突变体均未维持这种合成。用针对细胞外病毒蛋白或极晚期蛋白的抗血清进行的蛋白质免疫印迹分析表明,在非允许温度下,晚期结构蛋白减少,多角体蛋白减少10倍,且不存在p10。细胞内总RNA的Northern印迹分析表明,在非允许温度下,特异性晚期和极晚期转录本的合成量大幅减少,提示极晚期蛋白的缺失是病毒特异性转录受到抑制的结果。遗传分析表明,这些突变位于两个紧密连锁的基因中,这两个基因在调节极晚期转录和翻译的诱导中均很重要。

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