Simpson Deborah J, Dawson Lisa F, Fry John C, Rogers Hilary J, Day Martin J
Cardiff School of Biosciences, Cardiff University, Main Building, Park Place, Cardiff, UK.
Environ Biosafety Res. 2007 Jan-Jun;6(1-2):55-69. doi: 10.1051/ebr:2007027. Epub 2007 Sep 12.
RecA-mediated recombination requires regions of homology between donor and recipient DNA for successful integration. This paper investigates the effect of the relationship between the length of gene-sized inserts (434, 733, 2228 and 2400 bp) and flanking sequence homology (100 - ca. 11 000 bp) on transformation frequency in Acinetobacter baylyi strain BD413. Both insert size and size of the homologous region were varied, which improves on previous studies that kept insert size constant and varied only the homologous flank size. Transfer frequency of a non-homologous single small gene for gentamicin resistance (aac(3)I; 773 bp) was increased 18-fold when flanking homology was changed from about 2000 bp to 8000 bp, but was reduced 234-fold when two genes were inserted (nptII-gfp; 2400 bp) between similar homologous regions. To investigate the effect of smaller regions of flanking homology (100 - 2000 bp), a partial nptII-gfp deletion (434 bp) was restored. This confirmed that a minimum of 500 bp on each flank was required for transformation to be affected by flanking homology. The data obtained allowed development of a multiple regression equation to predict transformation frequency from homology, insert size and total fragment size for gene insertions. We also show that the ratio of flanking homology to insert size and not the total size of donor DNA is the most important variable determining transformation frequency. The equation developed was consistent with results previously reported by others, and so will be useful when using A. baylyi as a model for gene transfer by transformation in the laboratory, environment and for biosafety.
RecA介导的重组需要供体和受体DNA之间具有同源区域才能成功整合。本文研究了基因大小的插入片段(434、733、2228和2400 bp)长度与侧翼序列同源性(100 - 约11000 bp)之间的关系对拜氏不动杆菌BD413菌株转化频率的影响。插入片段大小和同源区域大小均有所变化,这改进了以往保持插入片段大小不变而仅改变同源侧翼大小的研究。当侧翼同源性从约2000 bp变为8000 bp时,庆大霉素抗性非同源单小基因(aac(3)I;773 bp)的转移频率增加了18倍,但当在相似同源区域之间插入两个基因(nptII - gfp;2400 bp)时,转移频率降低了234倍。为了研究较小侧翼同源区域(100 - 2000 bp)的影响,恢复了部分nptII - gfp缺失(434 bp)。这证实了每个侧翼至少需要500 bp才能使转化受到侧翼同源性的影响。所获得的数据使得能够建立一个多元回归方程,用于根据同源性、插入片段大小和基因插入的总片段大小预测转化频率。我们还表明,侧翼同源性与插入片段大小的比值而非供体DNA的总大小是决定转化频率的最重要变量。所建立的方程与其他人先前报道的结果一致,因此在将拜氏不动杆菌用作实验室、环境中转化基因转移及生物安全模型时将很有用。