Pierangeli A, Bucci M, Pagnotti P, Degener A M, Perez Bercoff R
Department of Cellular and Developmental Biology, University of Rome, Italy.
FEBS Lett. 1995 Nov 6;374(3):327-32. doi: 10.1016/0014-5793(95)01127-z.
A series of mutations were introduced in the 3'-terminal untranslated region (3'-UTR) of full-length infectious poliovirus cDNA clones, and following transfection of COS-1 cells the ability of these constructs to generate viable viral particles and/or to support viral RNA synthesis was assayed. Substitution of the 3'-UTR of poliovirus RNA with the equivalent sequences of HAV RNA abrogated viral RNA replication, whereas the introduction of extended 'foreign' sequences between the open reading frame and the 3'-UTR was well tolerated. Point mutation that either destabilized the stem-and-loop structure or altered the sequence of the loop in domain 'Y' (nomenclature as per Pilipenko et al., [Nuclei Acids Res. 20 (1992) 1739-1745]) abolished both the infectivity and viral RNA synthesis. These were not restored by compensatory mutation that reconstructed the native secondary structure of this domain, suggesting that the secondary/tertiary folding of the 3'-UTR is not the only determinant for template recognition at initiation of RNA synthesis, but rather that a specific primary sequence is indeed required.
在全长感染性脊髓灰质炎病毒cDNA克隆的3'末端非翻译区(3'-UTR)引入了一系列突变,转染COS-1细胞后,检测这些构建体产生有活力病毒颗粒和/或支持病毒RNA合成的能力。用甲型肝炎病毒RNA的等效序列替换脊髓灰质炎病毒RNA的3'-UTR可消除病毒RNA复制,而在开放阅读框和3'-UTR之间引入延伸的“外源”序列则具有良好的耐受性。使茎环结构不稳定或改变结构域“Y”中茎环序列的点突变(命名依据Pilipenko等人,[《核酸研究》20 (1992) 1739 - 1745])消除了感染性和病毒RNA合成。通过重建该结构域天然二级结构的补偿性突变并不能恢复这些功能,这表明3'-UTR的二级/三级折叠不是RNA合成起始时模板识别的唯一决定因素,而是确实需要特定的一级序列。