Delmas Stéphane, Matic Ivan
INSERM U571, Faculté de Médecine Necker-Enfants Malades Université Paris V, 156 rue Vaugirard, 75730 Paris Cedex 15, France.
DNA Repair (Amst). 2005 Feb 3;4(2):221-9. doi: 10.1016/j.dnarep.2004.09.008.
We studied how DNA divergence between recombining DNAs and the mismatch repair system modulate the SOS response in Escherichia coli. The observed positive log-linear correlation between SOS induction and DNA divergence, and the negative correlation between SOS induction and frequency of recombination, suggest that the level of SOS induction precisely reflects the difficulty of RecA protein to initiate a productive strand exchange process. Our results suggest that the mismatch repair system could contribute to this SOS induction more by affecting the RecA-catalyzed homology search than by acting on mismatched recombination intermediates. The propensity of the recombination machinery to promote recombination between the blocks of sequences with the highest identity results in the increasing ratios of merodiploids (partial diploids) over genuine recombinants (homologous replacements) with increasing DNA divergence. We discuss the role of molecular mechanisms involved in the control of the recombination between diverged DNA sequences in the maintenance of genomic stability and genome evolution.
我们研究了重组DNA之间的DNA差异以及错配修复系统如何调节大肠杆菌中的SOS反应。观察到的SOS诱导与DNA差异之间的正对数线性相关性,以及SOS诱导与重组频率之间的负相关性,表明SOS诱导水平精确反映了RecA蛋白启动有效链交换过程的难度。我们的结果表明,错配修复系统对这种SOS诱导的贡献更多地是通过影响RecA催化的同源性搜索,而不是作用于错配的重组中间体。随着DNA差异增加,重组机制促进具有最高同一性的序列块之间重组的倾向导致部分二倍体(部分双倍体)与真正重组体(同源替换)的比例增加。我们讨论了参与控制分歧DNA序列之间重组的分子机制在维持基因组稳定性和基因组进化中的作用。