Alexander L, Lu H H, Wimmer E
Department of Microbiology, School of Medicine, State University of New York at Stony Brook 11794.
Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1406-10. doi: 10.1073/pnas.91.4.1406.
A picornavirus hybrid genome was constructed in which the internal ribosomal entry site (IRES) of encephalomyocarditis virus was inserted between the 5' non-translated region and the open reading frame of poliovirus (PV), type 1 (Mahoney). Upon transfection into HeLa cells, the hybrid RNA replicated and yielded a derivative of PV (W1-PNENPO). The PV IRES could be removed from pPNENPO, which resulted in a hybrid picornavirus (W1-P108ENPO) in which the translation of the PV open reading frame normally promoted by the type 1 IRES of PV was promoted by the type 2 IRES of encephalomyocarditis virus. This result indicates that these elements are not likely to contain cis-acting elements necessary for PV replication or encapsidation. A foreign gene (bacterial chloramphenicol acetyltransferase, CAT) was inserted into pPNENPO cDNA between the PV and encephalomyocarditis virus IRES elements. The dicistronic RNA replicated in HeLa cells and yielded a derivative of PV (W1-DICAT) with a genome 17% longer than that of wild-type PV. CAT assays and immunoblot analyses showed that the viral RNA efficiently expressed the foreign gene in cell culture. The CAT activity diminished somewhat with each passage of the dicistronic virus, an observation which suggested that the inserted gene had a deleterious effect on viral replication. However, even after five virus passages, a significant quantity of the foreign gene was still expressed. Insertion of the open reading frame of luciferase (67 kDa) resulted in an RNA species that replicated and expressed luciferase for up to 20 hr after transfection. However, this elongated RNA was not encapsidated.
构建了一种微小核糖核酸病毒杂交基因组,其中脑心肌炎病毒的内部核糖体进入位点(IRES)插入到脊髓灰质炎病毒1型(Mahoney株)的5'非翻译区和开放阅读框之间。转染到HeLa细胞后,杂交RNA进行复制并产生了脊髓灰质炎病毒的一个衍生物(W1-PNENPO)。脊髓灰质炎病毒的IRES可从pPNENPO中去除,这产生了一种杂交微小核糖核酸病毒(W1-P108ENPO),其中脊髓灰质炎病毒开放阅读框的翻译通常由脊髓灰质炎病毒1型IRES促进,而在此杂交病毒中则由脑心肌炎病毒2型IRES促进。这一结果表明,这些元件不太可能包含脊髓灰质炎病毒复制或衣壳化所需的顺式作用元件。将一个外源基因(细菌氯霉素乙酰转移酶,CAT)插入到pPNENPO cDNA中脊髓灰质炎病毒和脑心肌炎病毒IRES元件之间。双顺反子RNA在HeLa细胞中复制,并产生了一种脊髓灰质炎病毒衍生物(W1-DICAT),其基因组比野生型脊髓灰质炎病毒长17%。CAT检测和免疫印迹分析表明,病毒RNA在细胞培养中能有效表达外源基因。双顺反子病毒每次传代后,CAT活性都会有所降低,这一观察结果表明插入的基因对病毒复制有有害影响。然而,即使在病毒传代五次后,仍有大量外源基因表达。插入荧光素酶的开放阅读框(67 kDa)产生了一种RNA分子,该分子在转染后能复制并表达荧光素酶长达20小时。然而,这种延长的RNA未被衣壳化。