Stancheva I, Koller T, Sogo J M
Institute of Cell Biology, ETH-Hönggerberg, 8093 Zurich, Switzerland.
EMBO J. 1999 Nov 15;18(22):6542-51. doi: 10.1093/emboj/18.22.6542.
In Escherichia coli, adenine methylation at the sequence GATC allows coupling of cellular processes to chromosome replication and the cell cycle. The transient presence of hemimethylated DNA after replication facilitates post-replicative mismatch repair, induces transcription of some genes and allows transposition of mobile elements. We were interested in estimating the half-life of hemimethylated DNA behind the replication fork in plasmid molecules and in determining whether Dam methyltransferase restores N6 adenine methylation simultaneously on both replicative arms. We show that remethylation takes place asynchronously on the leading and lagging daughter strands shortly after replication. On the leading arm the fully methylated adenine is restored approximately 2000 bp (corresponding to 2 s) behind the replication fork, while remethylation takes twice as long (at 3500-4000 bp or approximately 3.5-4 s) on the lagging replicative arm. This observation suggests that Dam remethylation of the lagging arm requires ligated Okazaki fragments.
在大肠杆菌中,序列GATC处的腺嘌呤甲基化可使细胞过程与染色体复制及细胞周期相偶联。复制后半甲基化DNA的短暂存在有助于复制后错配修复、诱导某些基因的转录并允许移动元件转座。我们感兴趣的是估算质粒分子中复制叉后半甲基化DNA的半衰期,并确定Dam甲基转移酶是否能同时在两条复制臂上恢复N6腺嘌呤甲基化。我们发现,复制后不久,前导链和滞后链上的重新甲基化是异步发生的。在前导臂上,完全甲基化的腺嘌呤在复制叉后约2000 bp(相当于2秒)处恢复,而在滞后复制臂上重新甲基化所需时间是其两倍(在3500 - 4000 bp处,即约3.5 - 4秒)。这一观察结果表明,滞后臂的Dam重新甲基化需要连接好的冈崎片段。