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Homologous Recombination-Experimental Systems, Analysis, and Significance.同源重组——实验系统、分析及意义
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Cyanide enhances hydrogen peroxide toxicity by recruiting endogenous iron to trigger catastrophic chromosomal fragmentation.氰化物通过募集内源性铁来引发灾难性的染色体断裂,从而增强过氧化氢的毒性。
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Homologous recombination is a primary pathway to repair DNA double-strand breaks generated during DNA rereplication.同源重组是修复DNA再复制过程中产生的DNA双链断裂的主要途径。
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dGTP starvation in Escherichia coli provides new insights into the thymineless-death phenomenon.大肠杆菌中的脱氧鸟苷三磷酸(dGTP)饥饿为无胸腺嘧啶死亡现象提供了新的见解。
PLoS Genet. 2014 May 8;10(5):e1004310. doi: 10.1371/journal.pgen.1004310. eCollection 2014 May.
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Replication fork inhibition in seqA mutants of Escherichia coli triggers replication fork breakage.大肠杆菌seqA突变体中的复制叉抑制会引发复制叉断裂。
Mol Microbiol. 2014 Jul;93(1):50-64. doi: 10.1111/mmi.12638. Epub 2014 May 23.
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Trimmomatic: a flexible trimmer for Illumina sequence data.Trimmomatic:一款适用于 Illumina 测序数据的灵活修剪工具。
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The precarious prokaryotic chromosome.易变的原核染色体。
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The chromosome cycle of prokaryotes.原核生物的染色体周期。
Mol Microbiol. 2013 Oct;90(2):214-27. doi: 10.1111/mmi.12372. Epub 2013 Sep 8.
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DNA replication origins.DNA 复制原点。
Cold Spring Harb Perspect Biol. 2013 Oct 1;5(10):a010116. doi: 10.1101/cshperspect.a010116.
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Trapping and breaking of in vivo nicked DNA during pulsed field gel electrophoresis.在脉冲场凝胶电泳中体内切口 DNA 的捕获和断裂。
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静态和动态因素限制大肠杆菌中的染色体复制复杂性,避免失控过度复制的危险。

Static and Dynamic Factors Limit Chromosomal Replication Complexity in Escherichia coli, Avoiding Dangers of Runaway Overreplication.

作者信息

Khan Sharik R, Mahaseth Tulip, Kouzminova Elena A, Cronan Glen E, Kuzminov Andrei

机构信息

Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801.

Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801

出版信息

Genetics. 2016 Mar;202(3):945-60. doi: 10.1534/genetics.115.184697. Epub 2016 Jan 22.

DOI:10.1534/genetics.115.184697
PMID:26801182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4788131/
Abstract

We define chromosomal replication complexity (CRC) as the ratio of the copy number of the most replicated regions to that of unreplicated regions on the same chromosome. Although a typical CRC of eukaryotic or bacterial chromosomes is 2, rapidly growing Escherichia coli cells induce an extra round of replication in their chromosomes (CRC = 4). There are also E. coli mutants with stable CRC∼6. We have investigated the limits and consequences of elevated CRC in E. coli and found three limits: the "natural" CRC limit of ∼8 (cells divide more slowly); the "functional" CRC limit of ∼22 (cells divide extremely slowly); and the "tolerance" CRC limit of ∼64 (cells stop dividing). While the natural limit is likely maintained by the eclipse system spacing replication initiations, the functional limit might reflect the capacity of the chromosome segregation system, rather than dedicated mechanisms, and the tolerance limit may result from titration of limiting replication factors. Whereas recombinational repair is beneficial for cells at the natural and functional CRC limits, we show that it becomes detrimental at the tolerance CRC limit, suggesting recombinational misrepair during the runaway overreplication and giving a rationale for avoidance of the latter.

摘要

我们将染色体复制复杂性(CRC)定义为同一染色体上复制程度最高的区域与未复制区域的拷贝数之比。尽管真核生物或细菌染色体的典型CRC为2,但快速生长的大肠杆菌细胞会在其染色体中诱导额外一轮复制(CRC = 4)。也存在CRC约为6的稳定的大肠杆菌突变体。我们研究了大肠杆菌中CRC升高的限度及后果,发现了三个限度:“自然”CRC限度约为8(细胞分裂更慢);“功能”CRC限度约为22(细胞分裂极其缓慢);以及“耐受”CRC限度约为64(细胞停止分裂)。虽然自然限度可能由日蚀系统间隔复制起始来维持,但功能限度可能反映了染色体分离系统的能力,而非专门机制,而耐受限度可能是由于限制复制因子的滴定所致。虽然重组修复对处于自然和功能CRC限度的细胞有益,但我们表明在耐受CRC限度时它会变得有害,这表明在失控的过度复制过程中会发生重组错配,并为避免后者提供了一个理由。