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腺病毒DNA复制的起始。II. 使用合成寡核苷酸腺病毒模板的结构要求。

Initiation of adenovirus DNA replication. II. Structural requirements using synthetic oligonucleotide adenovirus templates.

作者信息

Kenny M K, Hurwitz J

机构信息

Graduate Program in Molecular Biology, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.

出版信息

J Biol Chem. 1988 Jul 15;263(20):9809-17.

PMID:2838480
Abstract

Adenovirus (Ad) virions contain a 55-kDa terminal protein covalently linked to both 5'-ends of the linear duplex DNA genome. The origin of DNA replication is contained within the terminal 50 base pair of the inverted terminal repeats. In the accompanying paper (Kenny, M. K., Balogh, L. A., and Hurwitz, J. (1988) J. Biol. Chem. 263, 9801-9808), it was demonstrated that synthetic oligonucleotide templates which contain the Ad origin, but lack the 55-kDa terminal protein, can serve as templates for the initiation of Ad DNA replication. Partially duplex oligonucleotides that lacked up to 14 nucleotides from the 5'-end of the nontemplate (displaced) strand supported initiation as much as 20-fold more efficiently than fully duplex oligonucleotides. The removal of 18 nucleotides or more from the 5'-end of the displaced strand resulted in a sharp decrease in the ability of the DNA templates to support initiation. The poor template efficiency of certain DNAs could be explained by their inability to bind nuclear factor I. The initiation efficiency observed with other DNAs correlated with their ability to bind the preterminal protein-Ad DNA polymerase complex. At low concentrations of the Ad DNA-binding protein, protein-primed initiation was also observed on single-stranded DNAs. The single-stranded template strand of the Ad origin was at least 5-20-fold better at supporting initiation than other single-stranded DNAs. These findings suggest a model in which the 3'-end of the template strand is rendered single-stranded as a prerequisite for initiation of Ad DNA replication.

摘要

腺病毒(Ad)病毒粒子含有一种55千道尔顿的末端蛋白,该蛋白与线性双链DNA基因组的两个5'末端共价连接。DNA复制起点包含在反向末端重复序列的末端50个碱基对中。在随附的论文中(肯尼,M.K.,巴洛格,L.A.,和赫维茨,J.(1988年)《生物化学杂志》263,9801 - 9808),已证明含有腺病毒起点但缺乏55千道尔顿末端蛋白的合成寡核苷酸模板可作为腺病毒DNA复制起始的模板。从非模板(置换)链的5'末端缺失多达14个核苷酸的部分双链寡核苷酸比完全双链寡核苷酸支持起始的效率高20倍之多。从置换链的5'末端去除18个或更多核苷酸会导致DNA模板支持起始的能力急剧下降。某些DNA模板效率低下可由其无法结合核因子I来解释。观察到的其他DNA的起始效率与其结合末端前体蛋白 - 腺病毒DNA聚合酶复合物的能力相关。在低浓度的腺病毒DNA结合蛋白存在下,在单链DNA上也观察到蛋白引发的起始。腺病毒起点的单链模板链在支持起始方面比其他单链DNA至少好5 - 20倍。这些发现提示了一个模型,其中模板链的3'末端变为单链是腺病毒DNA复制起始的先决条件。

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