Ishikawa Ken, Handa Naofumi, Kobayashi Ichizo
Graduate Program in Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Tokyo 108-8639, Japan.
Nucleic Acids Res. 2009 Jun;37(11):3531-44. doi: 10.1093/nar/gkp214. Epub 2009 Apr 7.
Cleavage of a DNA replication fork leads to fork restoration by recombination repair. In prokaryote cells carrying restriction-modification systems, fork passage reduces genome methylation by the modification enzyme and exposes the chromosome to attack by the restriction enzyme. Various observations have suggested a relationship between the fork and Type I restriction enzymes, which cleave DNA at a distance from a recognition sequence. Here, we demonstrate that a Type I restriction enzyme preparation cleaves a model replication fork at its branch. The enzyme probably tracks along the DNA from an unmethylated recognition site on the daughter DNA and cuts the fork upon encountering the branch point. Our finding suggests that these restriction-modification systems contribute to genome maintenance through cell death and indicates that DNA replication fork cleavage represents a critical point in genome maintenance to choose between the restoration pathway and the destruction pathway.
DNA复制叉的断裂会通过重组修复导致叉的恢复。在携带限制修饰系统的原核细胞中,叉的通过会降低修饰酶对基因组的甲基化作用,并使染色体暴露于限制酶的攻击之下。各种观察结果表明,复制叉与I型限制酶之间存在关联,I型限制酶在距识别序列一定距离处切割DNA。在此,我们证明一种I型限制酶制剂会在其分支处切割模型复制叉。该酶可能从子代DNA上未甲基化的识别位点沿着DNA追踪,遇到分支点时切割复制叉。我们的发现表明,这些限制修饰系统通过细胞死亡促进基因组维护,并表明DNA复制叉的切割代表了基因组维护中在恢复途径和破坏途径之间进行选择的关键点。