Watanabe Y, Gauntt C J, Graham A F
J Virol. 1968 Sep;2(9):869-77. doi: 10.1128/JVI.2.9.869-877.1968.
A virus-induced ribonucleic acid (RNA) polymerase activity was found in L cells infected with type 3 reovirus. Most of the enzyme is associated with the "large particle" fraction of the infected cells. The enzyme first appeared at 3 to 5 hr after infection and increased in amount until 7 to 9 hr. All four ribonucleoside triphosphates are incorporated in vitro into an acid-insoluble form by the enzyme. The major part of the product formed in vitro is a double-stranded RNA indistinguishable from viral RNA by electrophoresis on polyacrylamide gel. Approximately 40% of the product is a single-stranded RNA of relatively small molecular weight. More than 95% of the nucleotides incorporated into double-stranded RNA by the enzyme are bound in internal 3'-5'-phosphodiester linkages extending back from both 3'- and 5'-termini of the RNA strands.
在感染3型呼肠孤病毒的L细胞中发现了一种病毒诱导的核糖核酸(RNA)聚合酶活性。大部分酶与感染细胞的“大颗粒”部分相关联。该酶在感染后3至5小时首次出现,并在数量上持续增加直至7至9小时。在体外,该酶能将所有四种核糖核苷三磷酸掺入酸不溶性形式。体外形成的产物的主要部分是一种双链RNA,通过聚丙烯酰胺凝胶电泳,它与病毒RNA无法区分。大约40%的产物是分子量相对较小的单链RNA。该酶掺入双链RNA中的核苷酸,超过95%以从RNA链的3'-和5'-末端向后延伸的内部3'-5'-磷酸二酯键结合。