School of Biological Sciences, Inje University, Gimhae, South Korea.
Mol Biotechnol. 2013 Jun;54(2):504-14. doi: 10.1007/s12033-012-9591-y.
Bacterial Artificial Chromosome (BAC) clones are widely used for retrieving genomic DNA sequences for gene targeting. In this study, low-copy-number plasmids pBAC-FB, pBAC-FC, and pBAC-DE, which carry the F plasmid replicon, were generated from pBACe3.6. pBAC-FB was successfully used to retrieve a sequence of a BAC that was resistant to retrieval by a high-copy-number plasmid via λ Red-mediated recombineering (gap-repair cloning). This plasmid was also used to retrieve two other genes from BAC, indicating its general usability retrieving genes from BAC. The retrieved genes were manipulated in generating targeting vectors for gene knockouts by recombineering. The functionality of the targeting vector was further validated in a targeting experiment with C57BL/6 embryonic stem cells. The low-copy-number plasmid pBAC-FB is a plasmid of choice to retrieve toxic DNA sequences from BACs and to manipulate them to generate gene-targeting constructs by recombineering.
细菌人工染色体 (BAC) 克隆广泛用于获取基因靶向的基因组 DNA 序列。在这项研究中,从 pBACe3.6 生成了携带 F 质粒复制子的低拷贝数质粒 pBAC-FB、pBAC-FC 和 pBAC-DE。pBAC-FB 成功地用于通过 λ Red 介导的重组(缺口修复克隆)回收对高拷贝数质粒具有抗性的 BAC 序列。该质粒还用于从 BAC 中回收另外两个基因,表明其通用性可从 BAC 中回收基因。通过重组回收的基因被用于生成基因敲除的靶向载体。通过 C57BL/6 胚胎干细胞的靶向实验进一步验证了靶向载体的功能。低拷贝数质粒 pBAC-FB 是从 BAC 中回收有毒 DNA 序列并通过重组操作它们来生成基因靶向构建体的首选质粒。