Wu X, Shaw J
Department of Plant Pathology, University of Kentucky, Lexington, 40546, USA.
Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):2981-4. doi: 10.1073/pnas.93.7.2981.
An essential step in the initiation of a virus infection is the release of the viral genome from the other constituents of the virus particle, a process referred to as uncoating. We have used reverse transcription and polymerase chain reaction amplification procedures to determine the rate and direction of in vivo uncoating of the rod-shaped tobacco mosaic virus. The virus particles contain a single 6.4-kb RNA molecule that lies between successive turns of a helical arrangement of coat protein subunits. When the particles are introduced into plant cells, the subunits are removed via a bidirectional uncoating mechanism. Within 2-3 min, the part of the viral RNA from the 5' end to a position >70% toward the 3' end has been freed of coat protein subunits. This is followed by removal of subunits from the 3' end of the RNA and sequential uncoating of the RNA in a 3'-to-5' direction. An internal region of the viral RNA is the final part to be uncoated. Progeny virus particles are detected in the cells 35-40 min after inoculation.
病毒感染起始的一个关键步骤是病毒基因组从病毒颗粒的其他成分中释放出来,这一过程称为脱壳。我们使用逆转录和聚合酶链反应扩增程序来确定棒状烟草花叶病毒在体内的脱壳速率和方向。病毒颗粒包含一个单一的6.4 kb RNA分子,该分子位于外壳蛋白亚基螺旋排列的连续螺旋之间。当病毒颗粒被引入植物细胞时,亚基通过双向脱壳机制被去除。在2-3分钟内,病毒RNA从5'端到3'端超过70%位置的部分已摆脱外壳蛋白亚基。随后,亚基从RNA的3'端被去除,RNA以3'到5'的方向依次脱壳。病毒RNA的内部区域是最后一个被脱壳的部分。接种后35-40分钟在细胞中检测到子代病毒颗粒。