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引物RNA合成所需的大肠杆菌引发酶/单链DNA结合蛋白/噬菌体G4 oriC复合物的结构

Structure of the Escherichia coli primase/single-strand DNA-binding protein/phage G4oric complex required for primer RNA synthesis.

作者信息

Sun W, Godson G N

机构信息

Biochemistry Department, New York University Medical Center, 550 First Avenue, New York 10016, USA.

出版信息

J Mol Biol. 1998 Mar 6;276(4):689-703. doi: 10.1006/jmbi.1997.1471.

Abstract

Escherichia coli primase/SSB/single-stranded phage G4oric is a simple system to study how primase interacts with DNA template to synthesize primer RNA for initiation of DNA replication. By a strategy of deletion analysis and antisense oligonucleotide protection on small single-stranded G4oric fragments, we have identified the DNA sequences required for binding primase and the critical location of single-strand DNA-binding (SSB) protein. Together with the previous data, we have defined the structure of the primase/SSB/G4oric priming complex. Two SSB tetramers bind to the G4oric secondary structure, which dictates the spacing of 3' and 5' bound adjacent SSB tetramers and leaves SSB-free regions on both sides of the stem-loop structure. Two primase molecules then bind separately to specific DNA sequences in the 3' and 5' SSB-free G4oric regions. Binding of the 3' SSB tetramer, upstream of the primer RNA initiation site, is also necessary for priming. The generation of a primase-recognition target by SSB phasing at DNA hairpin structures may be applicable to the binding of initiator proteins in other single-stranded DNA priming systems. Novel techniques used in this study include antisense oligonucleotide protection and RNA synthesis on an SSB-melted, double-stranded DNA template.

摘要

大肠杆菌引发酶/单链结合蛋白(SSB)/单链噬菌体G4 oriC是一个简单的系统,用于研究引发酶如何与DNA模板相互作用以合成引物RNA来启动DNA复制。通过对小单链G4 oriC片段进行缺失分析和反义寡核苷酸保护策略,我们确定了结合引发酶所需的DNA序列以及单链DNA结合(SSB)蛋白的关键位置。结合先前的数据,我们定义了引发酶/SSB/G4 oriC引发复合物的结构。两个SSB四聚体结合到G4 oriC二级结构上,这决定了3'和5'结合的相邻SSB四聚体的间距,并在茎环结构两侧留下无SSB区域。然后两个引发酶分子分别结合到3'和5'无SSB的G4 oriC区域中的特定DNA序列上。引物RNA起始位点上游的3' SSB四聚体的结合对于引发也是必需 的。通过在DNA发夹结构处进行SSB定相产生引发酶识别靶标,这可能适用于其他单链DNA引发系统中起始蛋白的结合。本研究中使用的新技术包括反义寡核苷酸保护以及在SSB解链的双链DNA模板上进行RNA合成。

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