Yolov A A, Shabarova Z A
Department of Chemistry, M.V. Lomonosov State University, Moscow, USSR.
Nucleic Acids Res. 1990 Jul 11;18(13):3983-6. doi: 10.1093/nar/18.13.3983.
Polymerase-mediated recombination based on DNA polymerase chain reactions (PCRs) has been used to carry out directed joining at a present point of two DNA fragments initially contained in a plasmid and a single-stranded synthetic DNA. The process includes copying of these fragments by PCR with generation of an overlapping homologous region. Such overlap of 12 base pairs in length was found to be sufficient to provide further DNA joining also by use of PCR.
基于DNA聚合酶链式反应(PCR)的聚合酶介导重组已被用于在当前点对最初包含在质粒和单链合成DNA中的两个DNA片段进行定向连接。该过程包括通过PCR复制这些片段并产生重叠的同源区域。发现长度为12个碱基对的这种重叠足以通过使用PCR进一步实现DNA连接。