Kuzminov A
Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403, USA.
Microbiol Mol Biol Rev. 1999 Dec;63(4):751-813, table of contents. doi: 10.1128/MMBR.63.4.751-813.1999.
Although homologous recombination and DNA repair phenomena in bacteria were initially extensively studied without regard to any relationship between the two, it is now appreciated that DNA repair and homologous recombination are related through DNA replication. In Escherichia coli, two-strand DNA damage, generated mostly during replication on a template DNA containing one-strand damage, is repaired by recombination with a homologous intact duplex, usually the sister chromosome. The two major types of two-strand DNA lesions are channeled into two distinct pathways of recombinational repair: daughter-strand gaps are closed by the RecF pathway, while disintegrated replication forks are reestablished by the RecBCD pathway. The phage lambda recombination system is simpler in that its major reaction is to link two double-stranded DNA ends by using overlapping homologous sequences. The remarkable progress in understanding the mechanisms of recombinational repair in E. coli over the last decade is due to the in vitro characterization of the activities of individual recombination proteins. Putting our knowledge about recombinational repair in the broader context of DNA replication will guide future experimentation.
尽管最初对细菌中的同源重组和DNA修复现象进行了广泛研究,而未考虑两者之间的任何关系,但现在人们认识到DNA修复和同源重组是通过DNA复制联系在一起的。在大肠杆菌中,双链DNA损伤主要在含有单链损伤的模板DNA上复制过程中产生,通过与同源完整双链体(通常是姐妹染色体)重组进行修复。两种主要类型的双链DNA损伤被导入两种不同的重组修复途径:子链缺口由RecF途径封闭,而解体的复制叉由RecBCD途径重新建立。噬菌体λ重组系统较为简单,其主要反应是利用重叠的同源序列连接两个双链DNA末端。过去十年中在理解大肠杆菌重组修复机制方面取得的显著进展得益于对单个重组蛋白活性的体外表征。将我们关于重组修复的知识置于DNA复制的更广泛背景下将指导未来的实验。