Departments of Biological Sciences and Chemistry, University of Southern California, Los Angeles, CA 90089-2910, USA.
Department of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706-1544, USA.
Nucleic Acids Res. 2024 Jun 24;52(11):6392-6405. doi: 10.1093/nar/gkae320.
We report that the Escherichia coli chromosome includes novel GC-rich genomic structural elements that trigger formation of post-replication gaps upon replisome passage. The two nearly perfect 222 bp repeats, designated Replication Risk Sequences or RRS, are each 650 kb from the terminus sequence dif and flank the Ter macrodomain. RRS sequence and positioning is highly conserved in enterobacteria. At least one RRS appears to be essential unless a 200 kb region encompassing one of them is amplified. The RRS contain a G-quadruplex on the lagging strand which impedes DNA polymerase extension producing lagging strand ssDNA gaps, $ \le$2000 bp long, upon replisome passage. Deletion of both RRS elements has substantial effects on global genome structure and topology. We hypothesize that RRS elements serve as topological relief valves during chromosome replication and segregation. There have been no screens for genomic sequences that trigger transient gap formation. Functional analogs of RRS could be widespread, possibly including some enigmatic G-quadruplexes in eukaryotes.
我们报告称,大肠杆菌染色体包含新型的 GC 丰富基因组结构元素,这些元素在复制体通过时会引发复制后间隙的形成。这两个几乎完美的 222 个碱基对重复序列,被指定为复制风险序列或 RRS,每个序列距离端序列 dif 约 650 kb,并且位于 Ter 宏结构域的两侧。RRS 序列和定位在肠杆菌中高度保守。至少有一个 RRS 似乎是必需的,除非扩增包含其中一个的 200 kb 区域。RRS 在滞后链上包含一个 G-四链体,该四链体阻碍 DNA 聚合酶的延伸,导致复制体通过时产生 2000 bp 长的滞后链 ssDNA 缺口。删除两个 RRS 元件对全局基因组结构和拓扑结构有重大影响。我们假设 RRS 元件在染色体复制和分离过程中充当拓扑安全阀。目前还没有针对引发瞬时间隙形成的基因组序列进行筛选。RRS 的功能类似物可能很广泛,可能包括真核生物中一些神秘的 G-四链体。