质粒
生物
重组DNA
低拷贝数
T-DNA二元系统
克隆(编程)
重组
分子生物学
遗传学
DNA
基因
载体(分子生物学)
计算机科学
程序设计语言
作者
David Summers,David J. Sherratt
出处
期刊:Cell
[Elsevier]
日期:1984-04-01
卷期号:36 (4): 1097-1103
被引量:431
标识
DOI:10.1016/0092-8674(84)90060-6
摘要
Although the natural multicopy plasmid CoIE1 is maintained stably under most growth conditions, plasmid cloning vectors related to it are relatively unstable, being lost at frequencies of 10(-2)-10(-5) per cell per generation. Evidence suggests that CoIE1 and related plasmids are partitioned randomly at cell division and that plasmid stability is correlated inversely with plasmid multimerization; factors or conditions that reduce multimerization increase stability. Cells containing plasmid multimers segregate plasmid-free cells because the multimers are maintained at lower copy numbers than monomers, as predicted by origin-counting models for copy number control. CoIE1 is stable because it encodes a determinant, cer, that is necessary for recA-, recF-, and recE-independent recombination events that efficiently convert any multimers to monomers. We have localized monomerizing and stability determinants of CoIE1 to within a 0.38 kb region that, when cloned into plasmid vectors, greatly increases their stability.
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