Centro de Investigaciones en Química Biológica de Córdoba, CIQUIBIC, UNC-CONICET, Departamento de Química Biológica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, República Argentina.
PLoS One. 2012;7(3):e33701. doi: 10.1371/journal.pone.0033701. Epub 2012 Mar 16.
Different studies have suggested that mutation rate varies at different positions in the genome. In this work we analyzed if the chromosomal context and/or the presence of GATC sites can affect the frameshift mutation rate in the Escherichia coli genome. We show that in a mismatch repair deficient background, a condition where the mutation rate reflects the fidelity of the DNA polymerization process, the frameshift mutation rate could vary up to four times among different chromosomal contexts. Furthermore, the mismatch repair efficiency could vary up to eight times when compared at different chromosomal locations, indicating that detection and/or repair of frameshift events also depends on the chromosomal context. Also, GATC sequences have been proved to be essential for the correct functioning of the E. coli mismatch repair system. Using bacteriophage heteroduplexes molecules it has been shown that GATC influence the mismatch repair efficiency in a distance- and number-dependent manner, being almost nonfunctional when GATC sequences are located at 1 kb or more from the mutation site. Interestingly, we found that in E. coli genomic DNA the mismatch repair system can efficiently function even if the nearest GATC sequence is located more than 2 kb away from the mutation site. The results presented in this work show that even though frameshift mutations can be efficiently generated and/or repaired anywhere in the genome, these processes can be modulated by the chromosomal context that surrounds the mutation site.
不同的研究表明,突变率在基因组的不同位置有所不同。在这项工作中,我们分析了染色体环境和/或 GATC 位点的存在是否会影响大肠杆菌基因组中的移码突变率。我们表明,在错配修复缺陷的背景下,突变率反映 DNA 聚合过程的保真度,移码突变率在不同的染色体环境中可能相差四倍。此外,在不同的染色体位置比较时,错配修复效率可能相差八倍,表明移码事件的检测和/或修复也取决于染色体环境。此外,GATC 序列已被证明是大肠杆菌错配修复系统正确运作的必要条件。使用噬菌体异源双链分子已经表明,GATC 以距离和数量依赖的方式影响错配修复效率,当 GATC 序列位于距突变位点 1kb 或更远时,几乎没有功能。有趣的是,我们发现大肠杆菌基因组 DNA 中的错配修复系统即使最近的 GATC 序列距离突变位点超过 2kb 也能有效发挥作用。本工作中的结果表明,尽管移码突变可以在基因组的任何地方有效地产生和/或修复,但这些过程可以被突变位点周围的染色体环境所调节。