Qiu Jianming, Cheng Fang, Pintel David
Life Sciences Center, University of Missouri--Columbia, 1201 Rollins Rd., Columbia, MO 65212, USA.
J Virol. 2007 Jul;81(13):6993-7000. doi: 10.1128/JVI.00244-07. Epub 2007 Apr 11.
The abundant R2 mRNA encoded by the single left-end promoter of Aleutian mink disease parvovirus is tricistronic; it not only expresses the capsid proteins VP1 and VP2 but is also the major source for the nonstructural protein NS2. A cis-acting sequence within the NS2 gene was shown to be required for efficient capsid protein production, and its effect displayed a distinct location dependence. Ribosome transit through the upstream NS2 gene region was necessary for efficient VP1 and VP2 expression; however, neither ablation nor improvement of the NS2 initiating AUG had an effect on capsid protein production, suggesting that the translation of the NS2 protein per se had little influence on VP1 and VP2 expression. Thus, proper control of the alternative translation of the tricistronic R2 mRNA, a process critical for viral replication, is governed in a complex manner.
由阿留申水貂病细小病毒单一左端启动子编码的丰富R2 mRNA是多顺反子的;它不仅表达衣壳蛋白VP1和VP2,也是非结构蛋白NS2的主要来源。NS2基因内的一个顺式作用序列被证明是高效衣壳蛋白产生所必需的,其作用表现出明显的位置依赖性。核糖体通过上游NS2基因区域的转运对于高效表达VP1和VP2是必要的;然而,NS2起始AUG的缺失或改善对衣壳蛋白产生均无影响,这表明NS2蛋白本身的翻译对VP1和VP2表达影响很小。因此,对多顺反子R2 mRNA的选择性翻译的适当控制,这一病毒复制的关键过程,是以一种复杂的方式调控的。