Castaneda S J, Wong T C
Department of Microbiology, University of Washington School of Medicine, Seattle 98195.
J Virol. 1989 Jul;63(7):2977-86. doi: 10.1128/JVI.63.7.2977-2986.1989.
The minus-sense RNA genome of measles virus serves as a template for synthesizing plus-sense RNAs of genomic length (antigenomes) and subgenomic length [poly(A)+ RNAs]. To elucidate how these different species are produced in vivo, RNA synthesized from the 3'-proximal N gene was characterized by Northern RNA blot and RNase protection analyses. The results showed that measles virus produced three size classes of plus-sense N-containing RNA species corresponding to monocistronic N RNA, bicistronic NP RNA, and antigenomes. Unlike vesicular stomatitis virus, measles virus does not produce a detectable free plus-sense leader RNA. Instead, although antigenomes invariably contain a leader sequence, monocistronic and bicistronic poly(A)+ N-containing RNAs are synthesized either without or with a leader sequence. We cloned and characterized a full-length cDNA representing a product of the latter type of synthesis. mRNAs and antigenomes appeared sequentially and in parallel with leaderless and leader-containing RNAs. These various RNA species accumulated concurrently throughout infection. However, cycloheximide preferentially inhibited accumulation of antigenomes and leader-containing RNA but not leaderless and subgenomic RNAs late in infection, suggesting that synthesis of the former RNA species requires a late protein function or a continuous supply of structural proteins or both. These results reveal a previously undescribed mechanism for RNA synthesis in measles virus.
麻疹病毒的负链RNA基因组作为模板,用于合成基因组长度(反基因组)和亚基因组长度[poly(A)+RNA]的正链RNA。为了阐明这些不同种类的RNA在体内是如何产生的,通过Northern RNA印迹和RNase保护分析对从3'-近端N基因合成的RNA进行了表征。结果表明,麻疹病毒产生了三种大小类别的含正链N的RNA种类,分别对应单顺反子N RNA、双顺反子NP RNA和反基因组。与水疱性口炎病毒不同,麻疹病毒不会产生可检测到的游离正链前导RNA。相反,尽管反基因组总是包含一个前导序列,但单顺反子和双顺反子含poly(A)+N的RNA在合成时可以没有前导序列,也可以带有前导序列。我们克隆并表征了一个代表后一种合成类型产物的全长cDNA。mRNA和反基因组与无前导序列和含前导序列的RNA依次平行出现。在整个感染过程中,这些不同的RNA种类同时积累。然而,放线菌酮在感染后期优先抑制反基因组和含前导序列RNA的积累,但不抑制无前导序列和亚基因组RNA的积累,这表明前一种RNA种类的合成需要晚期蛋白功能或结构蛋白的持续供应,或两者兼而有之。这些结果揭示了麻疹病毒中一种以前未描述的RNA合成机制。