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大肠杆菌复制后随链中的优先DNA二级结构诱变

Preferential DNA secondary structure mutagenesis in the lagging strand of replication in E. coli.

作者信息

Trinh T Q, Sinden R R

机构信息

Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, Ohio 45267-0524.

出版信息

Nature. 1991 Aug 8;352(6335):544-7. doi: 10.1038/352544a0.

Abstract

When present in single-stranded DNA, palindromic or quasi-palindromic sequences have the potential to form complex secondary structures, including hairpins, which may facilitate interstrand misalignment of direct repeats and be responsible for diverse types of replication-based mutations, including deletions, additions, frameshifts and duplications. In regions of palindromic symmetry, specific deletion events may involve the formation of a hairpin or other DNA secondary structures which can stabilize the misalignment of direct repeats. One model suggests that these deletions occur during DNA replication by slippage of the template strand and misalignment with the progeny strand. The concurrent DNA replication model, involving an asymmetric dimeric DNA polymerase III complex which replicates the leading and lagging strands, has significant implications for mutagenesis. The intermittent looping of the lagging strand template, and the fact that the lagging strand template may contain a region of single-stranded DNA the length of an Okazaki fragment, provides an opportunity for DNA secondary-structure formation and misalignment. Here we report our design of a palindromic fragment to create an 'asymmetric palindromic insert' in the chloramphenicol acetyltransferase gene of plasmid pBR325. The frequency with which the insert was deleted in Escherichia coli depends on the orientation of the gene in the plasmid. Our results suggest that replication-dependent deletion between direct repeats may occur preferentially in the lagging strand.

摘要

当存在于单链DNA中时,回文或准回文序列有可能形成复杂的二级结构,包括发夹结构,这可能会促进同向重复序列的链间错配,并导致多种基于复制的突变,包括缺失、插入、移码和重复。在回文对称区域,特定的缺失事件可能涉及发夹或其他DNA二级结构的形成,这些结构可以稳定同向重复序列的错配。一种模型认为,这些缺失是在DNA复制过程中由于模板链的滑动和与子代链的错配而发生的。同时进行的DNA复制模型,涉及一种不对称二聚体DNA聚合酶III复合物,它复制前导链和后随链,这对诱变有重要影响。后随链模板的间歇性成环,以及后随链模板可能包含一个冈崎片段长度的单链DNA区域,为DNA二级结构的形成和错配提供了机会。在此,我们报告了我们设计的一个回文片段,用于在质粒pBR325的氯霉素乙酰转移酶基因中创建一个“不对称回文插入”。该插入在大肠杆菌中被删除的频率取决于该基因在质粒中的方向。我们的结果表明,直接重复序列之间依赖复制的缺失可能优先发生在后随链中。

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