Bosher J, Leith I R, Temperley S M, Wells M, Hay R T
Department of Biochemistry and Microbiology, University of St Andrews, Fife, U.K.
J Gen Virol. 1991 Dec;72 ( Pt 12):2975-80. doi: 10.1099/0022-1317-72-12-2975.
Recombinant baculoviruses have been constructed which express the full-length nuclear factor I (NFI) protein or a derivative of NFI that contains only the DNA-binding domain of the protein in infected insect cells. Both proteins were purified from insect cells infected with the respective baculoviruses and tested for their ability to cooperate with the adenovirus type 2 (Ad2) DNA-binding protein during virus replication. DNase I protection experiments demonstrated that the viral DNA-binding protein increased the affinity of both the full-length NFI and the DNA-binding domain of NFI for their recognition site in the Ad2 origin of DNA replication. As a consequence, the NFI-dependent increase in the efficiency of DNA replication observed upon addition of viral DNA-binding protein was the same when the full-length or DNA-binding domain derivative of NFI was added. Thus it appears that all of the activities associated with the ability of NFI to stimulate Ad2 DNA replication are located within the DNA-binding domain of the protein.
已构建出重组杆状病毒,其在受感染的昆虫细胞中表达全长核因子I(NFI)蛋白或仅包含该蛋白DNA结合结构域的NFI衍生物。两种蛋白均从感染了相应杆状病毒的昆虫细胞中纯化出来,并测试了它们在病毒复制过程中与2型腺病毒(Ad2)DNA结合蛋白协同作用的能力。DNase I保护实验表明,病毒DNA结合蛋白增加了全长NFI及其NFI的DNA结合结构域对它们在Ad2 DNA复制起点中识别位点的亲和力。因此,当添加NFI的全长或DNA结合结构域衍生物时,在添加病毒DNA结合蛋白后观察到的NFI依赖性DNA复制效率的增加是相同的。因此,似乎与NFI刺激Ad2 DNA复制能力相关的所有活性都位于该蛋白的DNA结合结构域内。