Backert S, Kunnimalaiyaan M, Börner T, Nielsen B L
Department of Botany and Microbiology, Auburn University, 101 Life Sciences Building, Auburn, AL, 36849, USA.
J Mol Biol. 1998 Dec 11;284(4):1005-15. doi: 10.1006/jmbi.1998.2254.
According to the endosymbiotic theory, mitochondrial genomes evolved from the chromosome of an alpha-proteobacterium-like ancestor and developed during evolution an extraordinary variation in size, structure and replication. We studied in vitro DNA replication of the mitochondrial circular plasmid mp1 (1309 bp) from the higher plant Chenopodium album (L.) as a model system that replicates in a manner reminiscent of bacterial rolling circle plasmids. Several mp1 subclones were tested for their ability to support DNA replication using a newly developed in vitro system. Neutral/neutral two-dimensional gel electrophoresis of the in vitro products revealed typical simple Y patterns of intermediates consistent with a rolling circle type of replication. Replication activity was very high for a BamHI-restricted total plasmid DNA clone, a 464 bp BamHI/KpnI fragment and a 363 bp BamHI/SmaI fragment. Further subcloning of a 148 bp BamHI/EcoRI fragment resulted in the strongest in vitro DNA replication activity, while a 1161 bp-template outside of this region resulted in a substantial loss of activity. Electron microscopic studies of in vitro DNA replication products from the highly active clones also revealed sigma-shaped molecules. These results support our in vivo data for the presence of a predominant replication origin between positions 628 and 776 on the plasmid map. This sequence shares homology with double-stranded rolling circle origin (dso) or transfer origin (oriT) nicking motifs from bacterial plasmids. mp1 is the first described rolling circle plasmid in eukaryotes.
根据内共生理论,线粒体基因组从类似α-变形菌的祖先染色体进化而来,在进化过程中其大小、结构和复制发生了显著变化。我们以高等植物藜(Chenopodium album (L.))的线粒体环状质粒mp1(1309 bp)为模型系统,研究其体外DNA复制,该质粒的复制方式类似于细菌滚环质粒。使用新开发的体外系统测试了几个mp1亚克隆支持DNA复制的能力。体外产物的中性/中性二维凝胶电泳显示出典型的简单Y型中间体,与滚环复制类型一致。对于BamHI酶切的总质粒DNA克隆、一个464 bp的BamHI/KpnI片段和一个363 bp的BamHI/SmaI片段,复制活性非常高。对一个148 bp的BamHI/EcoRI片段进一步亚克隆产生了最强的体外DNA复制活性,而该区域外的一个1161 bp模板导致活性大幅丧失。对高活性克隆的体外DNA复制产物进行电子显微镜研究也揭示了σ形分子。这些结果支持了我们体内数据,即在质粒图谱上628和776位之间存在一个主要的复制起点。该序列与细菌质粒的双链滚环起点(dso)或转移起点(oriT)切口基序具有同源性。mp1是真核生物中首次描述的滚环质粒。