Kurg A, Sommer G, Metspalu A
Institute of Molecular and Cell Biology, Estonian Biocenter, Tartu University.
Virology. 1995 Aug 20;211(2):434-42. doi: 10.1006/viro.1995.1425.
An RNA secondary structure of the bovine leukemia virus (BLV) 5'-terminal RNA sequence was constructed by computer-assisted RNA secondary structure analysis. Mutations were created in the noncoding region (NCR) of BLV, which contains a conserved consensus sequence, to disrupt predicted secondary structure of this region. After transfection of these constructs into FLK-BLV cells and analysis of viral particles a reduction in mutant RNA content was observed relative to that of unmutated vector RNA. The packaging efficiency of the mutant with a substitution in the consensus sequence was reduced threefold and that of the mutant with a deleted 5' NCR was reduced fivefold. We conclude that predicted RNA secondary structure and/or nucleotide sequence of the BLV noncoding region is essential for BLV RNA packaging in vivo.
通过计算机辅助的RNA二级结构分析构建了牛白血病病毒(BLV)5'-末端RNA序列的RNA二级结构。在BLV的非编码区(NCR)中引入突变,该区域包含一个保守的共有序列,以破坏该区域预测的二级结构。将这些构建体转染到FLK-BLV细胞中并分析病毒颗粒后,观察到突变RNA含量相对于未突变载体RNA有所降低。共有序列发生取代的突变体的包装效率降低了三倍,而5' NCR缺失的突变体的包装效率降低了五倍。我们得出结论,BLV非编码区预测的RNA二级结构和/或核苷酸序列对于体内BLV RNA包装至关重要。