Dunoyer P, Herzog E, Hemmer O, Ritzenthaler C, Fritsch C
Institut de Biologie Moléculaire des Plantes, Centre National de la Recherche Scientifique, 67084 Strasbourg Cedex, France.
J Virol. 2001 Feb;75(4):1941-8. doi: 10.1128/JVI.75.4.1941-1948.2001.
RNA-1 of peanut clump pecluvirus (PCV) encodes N-terminally overlapping proteins which contain helicase-like (P131) and polymerase-like (P191) domains and is able to replicate in the absence of RNA-2 in protoplasts of tobacco BY-2 cells. RNA-1 also encodes P15, which is expressed via a subgenomic RNA. To investigate the role of P15, we analyzed RNA accumulation in tobacco BY-2 protoplasts inoculated with RNA-1 containing mutations in P15. For all the mutants, the amount of progeny RNA-1 produced was significantly lower than that obtained for wild-type RNA-1. If RNA-2 was included in the inoculum, the accumulation of both progeny RNAs was diminished, but near-normal yields of both could be recovered if the inoculum was supplemented with a small, chimeric viral replicon expressing P15, demonstrating that P15 has an effect on viral RNA accumulation. To further analyze the role of P15, transcripts were produced expressing P15 fused to enhanced green fluorescent protein (EGFP). Following inoculation to protoplasts, epifluorescence microscopy revealed that P15 accumulated as spots around the nucleus and in the cytoplasm. Intracellular sites of viral RNA synthesis were visualized by laser scanning confocal microscopy of infected protoplasts labeled with 5-bromouridine 5'-triphosphate (BrUTP). BrUTP labeling also occurred in spots distributed within the cytoplasm and around the nucleus. However, the BrUTP-labeled RNA and EGFP/P15 very rarely colocalized, suggesting that P15 does not act primarily at sites of viral replication but intervenes indirectly to control viral accumulation levels.
花生丛簇病毒(PCV)的RNA-1编码N端重叠蛋白,这些蛋白包含解旋酶样结构域(P131)和聚合酶样结构域(P191),并且能够在烟草BY-2细胞原生质体中在没有RNA-2的情况下进行复制。RNA-1还编码P15,它通过亚基因组RNA进行表达。为了研究P15的作用,我们分析了接种含有P15突变的RNA-1的烟草BY-2原生质体中的RNA积累情况。对于所有突变体,产生的子代RNA-1的量显著低于野生型RNA-1。如果接种物中包含RNA-2,两种子代RNA的积累都会减少,但如果接种物中补充表达P15的小型嵌合病毒复制子,则两种子代RNA的产量都可以恢复到接近正常水平,这表明P15对病毒RNA积累有影响。为了进一步分析P15的作用,我们制备了与增强型绿色荧光蛋白(EGFP)融合表达P15的转录本。接种到原生质体后,落射荧光显微镜观察发现P15在细胞核周围和细胞质中以斑点形式积累。通过对用5-溴尿苷5'-三磷酸(BrUTP)标记的受感染原生质体进行激光扫描共聚焦显微镜观察,可视化了病毒RNA合成的细胞内位点。BrUTP标记也出现在细胞质内和细胞核周围分布的斑点中。然而,BrUTP标记的RNA和EGFP/P15很少共定位,这表明P15主要不是在病毒复制位点起作用,而是间接干预以控制病毒积累水平。