Parada C A, Marians K J
Program in Molecular Biology, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.
J Biol Chem. 1991 Oct 5;266(28):18895-906.
pBR322 DNA can be replicated via a DNA A-dependent pathway mediated by its binding to the two DNA A-binding sites (dnaA boxes) present near the plasmid origin. DNA synthesis requires the transcription of RNA II (the leading-strand primer precursor) to generate a specific unwound structure in the region containing the dnaA boxes. In this structure, the DNA containing the dnaA boxes can take the form of either a RNA II-parental H strand pBR322 DNA hybrid opposed by the displaced parental L strand (in the absence of RNase H and DNA polymerase I), or a nascent leading strand-parental H strand DNA duplex opposed by the displaced parental L strand (in the presence of RNase H and DNA polymerase I). These findings defined three types of potential sites for productive DNA A binding: (i) the displaced parental L single strand, (ii) a hairpin formed by the inverted repeat of the two dnaA boxes, and (iii) either the RNA-DNA duplex or the nascent leading strand-parental DNA duplex. By using a combination of: (i) inhibition of the replication of a plasmid carrying oriC by oligonucleotides of various dnaA box sequences and conformation, (ii) a gel mobility shift assay to measure DNA A binding to the same oligonucleotide substrates, (iii) replication of pBR322 DNA templates with either one or no dnaA box, and (iv) photocross-linking to demonstrate DNA A binding to an RNA-DNA hybrid, evidence is presented here that DNA A-mediated pBR322 DNA replication proceeds by a mechanism in which DNA A binds to the duplex side of the unwound origin structures and loads the DNA B protein in trans to the displaced parental L strand DNA.
pBR322 DNA可通过一种依赖DNA A的途径进行复制,该途径由其与质粒复制起点附近存在的两个DNA A结合位点(dnaA框)结合介导。DNA合成需要转录RNA II(前导链引物前体),以在包含dnaA框的区域产生特定的解旋结构。在这种结构中,包含dnaA框的DNA可以采取以下两种形式之一:一是与被置换的亲本L链相对的RNA II-亲本H链pBR322 DNA杂交体(在没有RNase H和DNA聚合酶I的情况下),二是与被置换的亲本L链相对的新生前导链-亲本H链DNA双链体(在有RNase H和DNA聚合酶I的情况下)。这些发现确定了三种可能发生有效DNA A结合的位点类型:(i)被置换的亲本L单链,(ii)由两个dnaA框的反向重复形成的发夹结构,以及(iii)RNA-DNA双链体或新生前导链-亲本DNA双链体。通过以下方法的组合:(i)用各种dnaA框序列和构象的寡核苷酸抑制携带oriC的质粒的复制,(ii)用凝胶迁移率变动分析来测量DNA A与相同寡核苷酸底物的结合,(iii)用含有一个或不含dnaA框的pBR322 DNA模板进行复制,以及(iv)光交联以证明DNA A与RNA-DNA杂交体的结合,本文提供的证据表明,DNA A介导的pBR322 DNA复制通过一种机制进行,即DNA A结合到解旋的复制起点结构的双链侧,并将DNA B蛋白反式加载到被置换的亲本L链DNA上。