Moes Lorin, Wirth Manfred
Evolva, CH-4123 Allschwil, Switzerland.
Virol J. 2007 Nov 22;4:124. doi: 10.1186/1743-422X-4-124.
Bovine viral diarrhea virus (BVDV) is the prototype representative of the pestivirus genus in the Flaviviridae family. It has been shown that the initiation of translation of BVDV RNA occurs by an internal ribosome entry mechanism mediated by the 5' untranslated region of the viral RNA 1. The 5' and 3' boundaries of the IRES of the cytopathic BVDV NADL have been mapped and it has been suggested that the IRES extends into the coding of the BVDV polyprotein 2. A putative pseudoknot structure has been recognized in the BVDV 5'UTR in close proximity to the AUG start codon. A pseudoknot structure is characteristic for flavivirus IRESes and in the case of the closely related classical swine fever virus (CSFV) and the more distantly related Hepatitis C virus (HCV) pseudoknot function in translation has been demonstrated.
To characterize the BVDV IRESes in detail, we studied the BVDV translational initiation by transfection of dicistronic expression plasmids into mammalian cells. A region coding for the amino terminus of the BVDV SD-1 polyprotein contributes considerably to efficient initiation of translation. The translation efficiency mediated by the IRES of BVDV strains NADL and SD-1 approximates the poliovirus type I IRES directed translation in BHK cells. Compared to the poliovirus IRES increased expression levels are mediated by the BVDV IRES of strain SD-1 in murine cell lines, while lower levels are observed in human cell lines. Site directed mutagenesis revealed that a RNA pseudoknot upstream of the initiator AUG is an important structural element for IRES function. Mutants with impaired ability to base pair in stem I or II lost their translational activity. In mutants with repaired base pairing either in stem 1 or in stem 2 full translational activity was restored. Thus, the BVDV IRES translation is dependent on the pseudoknot integrity. These features of the pestivirus IRES are reminiscent of those of the classical swine fever virus, a pestivirus, and the hepatitis C viruses, another genus of the Flaviviridae.
The IRES of the non-cytopathic BVDV SD-1 strain displays features known from other pestivirus IRESes. The predicted pseudoknot in the 5'UTR of BVDV SD-1 virus represents an important structural element in BVDV translation.
牛病毒性腹泻病毒(BVDV)是黄病毒科瘟病毒属的原型代表。研究表明,BVDV RNA的翻译起始是通过由病毒RNA 1的5'非翻译区介导的内部核糖体进入机制进行的。细胞病变性BVDV NADL的内部核糖体进入位点(IRES)的5'和3'边界已被定位,并且有人提出IRES延伸到BVDV多聚蛋白的编码区2。在BVDV 5'非翻译区靠近AUG起始密码子处已识别出一个假定的假结结构。假结结构是黄病毒IRES的特征,并且在密切相关的经典猪瘟病毒(CSFV)和更远相关的丙型肝炎病毒(HCV)的情况下,已证明假结在翻译中起作用。
为了详细表征BVDV IRES,我们通过将双顺反子表达质粒转染到哺乳动物细胞中来研究BVDV的翻译起始。编码BVDV SD-1多聚蛋白氨基末端的区域对翻译的有效起始有很大贡献。BVDV毒株NADL和SD-1的IRES介导的翻译效率接近BHK细胞中I型脊髓灰质炎病毒IRES指导的翻译。与脊髓灰质炎病毒IRES相比,SD-1毒株的BVDV IRES在鼠细胞系中介导的表达水平增加,而在人细胞系中观察到较低水平。定点诱变表明,起始AUG上游的RNA假结是IRES功能的重要结构元件。在茎I或II中碱基配对能力受损的突变体失去了它们的翻译活性。在茎1或茎2中碱基配对修复的突变体中,完全恢复了翻译活性。因此,BVDV IRES翻译依赖于假结完整性。瘟病毒IRES的这些特征让人想起瘟病毒经典猪瘟病毒和黄病毒科另一属的丙型肝炎病毒的特征。
非细胞病变性BVDV SD-1毒株的IRES表现出其他瘟病毒IRES已知的特征。BVDV SD-1病毒5'非翻译区中预测的假结代表BVDV翻译中的一个重要结构元件。