Aleksenko A Y
Institute of Genetics and Selection of Industrial Microorganisms, Moscow, Russia.
Curr Genet. 1994 Oct;26(4):352-8. doi: 10.1007/BF00310500.
Transforming DNAs form cointegrates in Aspergillus nidulans by homologous and non-homologous recombination as well as by end-to-end ligation of linear fragments. This process has been studied by means of a model in which the linkage of a marker gene to the origin of autonomous replication AMA1 was selected for. Recombinant plasmids were rescued into Escherichia coli and subjected to restriction mapping and sequence analysis. It was shown that circular DNA molecules recombined predominantly within homologous fragments. Linear DNA fragments integrated into circular plasmids by invasion of their ends into random non-homologous sites, but exhibited some bias in choice of a target sequence. Cointegrates of multiple plasmid copies were often observed. In some of the plasmids analysed, short duplications of the target sequence flanking an inserted linear DNA fragment have been revealed.
通过同源和非同源重组以及线性片段的端对端连接,转化DNA在构巢曲霉中形成共整合体。这个过程已通过一个模型进行研究,在该模型中选择了一个标记基因与自主复制起点AMA1的连接。重组质粒被拯救到大肠杆菌中,并进行限制性图谱分析和序列分析。结果表明,环状DNA分子主要在同源片段内重组。线性DNA片段通过其末端侵入随机的非同源位点整合到环状质粒中,但在靶序列的选择上表现出一定的偏向性。经常观察到多个质粒拷贝的共整合体。在一些分析的质粒中,已发现插入的线性DNA片段两侧的靶序列有短重复序列。