Hagen M, Tiley L, Chung T D, Krystal M
Department of Virology, Bristol-Myers Squibb Pharmaceutical Research Institute, Wallingford, CT 06492.
J Gen Virol. 1995 Mar;76 ( Pt 3):603-11. doi: 10.1099/0022-1317-76-3-603.
An in vitro cleavage/initiation assay was used to analyse cleavage site choice and transcription initiation by the influenza virus polymerase. A synthetic mRNA which is cleaved by the polymerase to produce a single 11 base primer fragment was altered around this cleavage site. Depending upon the mutations made, alternative cleavage sites were used. This system was then used in extracts from recombinant vaccinia virus infected cells which express the polymerase. These extracts require the addition of a synthetic vRNA in order to induce cleavage and initiation activity. The data show that the choice of cleavage site is wholely controlled by the mRNA and does not depend upon interactions with the vRNA template. However, the site of initiation of the cleaved primer on the template is influenced by template-primer interactions.
利用体外切割/起始分析来分析流感病毒聚合酶的切割位点选择和转录起始。一种被聚合酶切割以产生单个11个碱基引物片段的合成mRNA在该切割位点周围被改变。根据所做的突变,使用了替代的切割位点。然后将该系统用于表达聚合酶的重组痘苗病毒感染细胞的提取物中。这些提取物需要添加合成的vRNA以诱导切割和起始活性。数据表明,切割位点的选择完全由mRNA控制,并不依赖于与vRNA模板的相互作用。然而,切割后的引物在模板上的起始位点受模板-引物相互作用的影响。