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Specific mutations within the AT-rich region of a plasmid replication origin affect either origin opening or helicase loading

机译:质粒复制起点富含AT的区域内的特定突变会影响起点开启或解旋酶负载

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摘要

Prokaryotic and eukaryotic replicons possess a distinctive region containing a higher than average number of adenine and thymine residues (the AT-rich region) where, during the process of replication initiation, the initial destabilization (opening) of the double helix takes place. In many prokaryotic origins, this region consists of repeated 13-mer motifs whose function has not yet been specified. Here we identify specific mutations within the 13-mer sequences of the broad-host-range plasmid RK2 that can result in defective origin opening or that do not affect opening but induce defects in helicase loading. We also show that after the initial recruitment of helicase at the DnaA-box sequences of the plasmid origin, the helicase is translocated to the AT-rich region in a reaction requiring specific sequence of the 13-mers and appropriate facing of the origin motifs. Our results demonstrate that specific sequences within the AT-rich region of a replication origin are required for either origin opening or helicase loading.
机译:原核和真核复制子具有一个独特的区域,该区域包含高于平均水平的腺嘌呤和胸腺嘧啶残基(富含AT的区域),该区域在复制起始过程中发生了双螺旋的初始失稳(开放)。在许多原核生物起源中,该区域由重复的13聚体基序组成,其功能尚未确定。在这里,我们确定了宽宿主范围质粒RK2的13-mer序列内的特定突变,这些突变可能导致起始位点有缺陷,或者不影响开放性,但导致解旋酶上的缺陷。我们还表明,最初在质粒来源的DnaA-box序列中加入解旋酶后,在需要13-mers特定序列和起源基序适当面对的反应中,解旋酶易位至富含AT的区域。我们的结果表明,复制起点的富含AT区域内的特定序列对于起点开启或解旋酶加载都是必需的。

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