Duechler M, Skern T, Blaas D, Berger B, Sommergruber W, Kuechler E
Institut für Biochemie, der Universitaet Wien, Vienna, Austria.
Virology. 1989 Jan;168(1):159-61. doi: 10.1016/0042-6822(89)90414-5.
A complete cDNA copy of human rhinovirus serotype 2 RNA was placed under the control of a T7 RNA polymerase promoter. An in vitro transcribed RNA containing two extra G residues at the 5' end gave rise to plaques on transfection into HeLa cells. The efficiency was approximately half that obtained with viral RNA. On the contrary, an in vitro synthesized RNA containing 16 additional nucleotides at the 5' end was not infectious. This ability to make an infectious in vitro transcribed RNA will be useful in studying the characteristics of viruses using the human rhinoviral minor group receptor.
人鼻病毒2型RNA的完整cDNA拷贝置于T7 RNA聚合酶启动子的控制之下。5'端含有两个额外G残基的体外转录RNA转染HeLa细胞后产生了噬斑。其效率约为病毒RNA的一半。相反,5'端含有16个额外核苷酸的体外合成RNA没有感染性。这种制备具有感染性的体外转录RNA的能力将有助于利用人鼻病毒小群受体研究病毒的特性。