Restrepo-Hartwig M, Ahlquist P
Institute for Molecular Virology, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
J Virol. 1999 Dec;73(12):10303-9. doi: 10.1128/JVI.73.12.10303-10309.1999.
The universal membrane association of positive-strand RNA virus RNA replication complexes is implicated in their function, but the intracellular membranes used vary among viruses. Brome mosaic virus (BMV) encodes two mutually interacting RNA replication proteins: 1a, which contains RNA capping and helicase-like domains, and the polymerase-like 2a protein. In cells from the natural plant hosts of BMV, 1a and 2a colocalize on the endoplasmic reticulum (ER). 1a and 2a also direct BMV RNA replication and subgenomic mRNA synthesis in the yeast Saccharomyces cerevisiae, but whether the distribution of 1a, 2a, and active replication complexes in yeast duplicates that in plant cells has not been determined. For yeast expressing 1a and 2a and replicating BMV genomic RNA3, we used double-label confocal immunofluorescence to define the localization of 1a, 2a, and viral RNA and to explore the determinants of replication complex targeting. As in plant cells, 1a and 2a colocalized on and were retained on the yeast ER, with no detectable accumulation in the Golgi apparatus. 1a and 2a were distributed over most of the ER surface, with strongest accumulation on the perinuclear ER. In vivo labeling with bromo-UTP showed that the sites of 1a and 2a accumulation were the sites of nascent viral RNA synthesis. In situ hybridization showed that completed viral RNA products accumulated predominantly in the immediate vicinity of replication complexes but that some, possibly more mature cells also accumulated substantial viral RNA in the surrounding cytoplasm distal to replication complexes. Additionally, we find that 1a localizes to the ER when expressed in the absence of other viral factors. These results show that BMV RNA replication in yeast duplicates the normal localization of replication complexes, reveal the intracellular distribution of RNA replication products, and show that 1a is at least partly responsible for the ER localization and retention of the RNA replication complex.
正链RNA病毒RNA复制复合体与通用膜的结合与其功能相关,但不同病毒所利用的细胞内膜有所不同。雀麦花叶病毒(BMV)编码两种相互作用的RNA复制蛋白:1a,其包含RNA封端和螺旋酶样结构域,以及聚合酶样的2a蛋白。在BMV天然植物宿主的细胞中,1a和2a在内质网(ER)上共定位。1a和2a还能在酿酒酵母中指导BMV RNA复制和亚基因组mRNA合成,但1a、2a和活性复制复合体在酵母中的分布是否与植物细胞中的相同尚未确定。对于表达1a和2a并复制BMV基因组RNA3的酵母,我们使用双标记共聚焦免疫荧光来确定1a、2a和病毒RNA的定位,并探索复制复合体靶向的决定因素。与植物细胞一样,1a和2a在酵母ER上共定位并保留在ER上,在高尔基体中未检测到积累。1a和2a分布在大部分ER表面,在核周ER上积累最强。用溴尿苷三磷酸(bromo-UTP)进行体内标记表明,1a和2a积累的位点是新生病毒RNA合成的位点。原位杂交显示,完整的病毒RNA产物主要在复制复合体的紧邻区域积累,但一些可能更成熟的细胞在复制复合体远端周围的细胞质中也积累了大量病毒RNA。此外,我们发现1a在没有其他病毒因子的情况下表达时定位于ER。这些结果表明,酵母中的BMV RNA复制复制了复制复合体的正常定位,揭示了RNA复制产物的细胞内分布,并表明1a至少部分负责RNA复制复合体的ER定位和保留。