首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach
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Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach

机译:使用新型转座子介导的方法确定大肠杆菌中DNA元素的最佳染色体位置

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摘要

The optimal chromosomal position(s) of a given DNA element was/were determined by transposon-mediated random insertion followed by fitness selection. In bacteria, the impact of the genetic context on the function of a genetic element can be difficult to assess. Several mechanisms, including topological effects, transcriptional interference from neighboring genes, and/or replication-associated gene dosage, may affect the function of a given genetic element. Here, we describe a method that permits the random integration of a DNA element into the chromosome of Escherichia coli and select the most favorable locations using a simple growth competition experiment. The method takes advantage of a well-described transposon-based system of random insertion, coupled with a selection of the fittest clone(s) by growth advantage, a procedure that is easily adjustable to experimental needs. The nature of the fittest clone(s) can be determined by whole-genome sequencing on a complex multi-clonal population or by easy gene walking for the rapid identification of selected clones. Here, the non-coding DNA region DARS2, which controls the initiation of chromosome replication in E. coli, was used as an example. The function of DARS2 is known to be affected by replication-associated gene dosage; the closer DARS2 gets to the origin of DNA replication, the more active it becomes. DARS2 was randomly inserted into the chromosome of a DARS2-deleted strain. The resultant clones containing individual insertions were pooled and competed against one another for hundreds of generations. Finally, the fittest clones were characterized and found to contain DARS2 inserted in close proximity to the original DARS2 location.
机译:通过转座子介导的随机插入,然后进行适应性选择,确定了给定DNA元件的最佳染色体位置。在细菌中,遗传背景对遗传元件功能的影响可能难以评估。几种机制,包括拓扑效应,来自邻近基因的转录干扰和/或与复制相关的基因剂量,可能会影响给定遗传元件的功能。在这里,我们描述了一种方法,该方法允许将DNA元素随机整合到大肠杆菌的染色体中,并使用简单的生长竞争实验选择最有利的位置。该方法利用了众所周知的基于转座子的随机插入系统,并通过生长优势选择了最适合的克隆,该过程很容易适应实验需要。最适合的克隆的性质可以通过对复杂的多克隆种群进行全基因组测序或通过简单的基因步移来快速鉴定所选克隆来确定。在此,以控制大肠杆菌中的染色体复制的开始的非编码DNA区域DARS2为例。已知DARS2的功能受复制相关基因剂量的影响。 DARS2离DNA复制起点越近,它变得越活跃。将DARS2随机插入缺失了DARS2的菌株的染色体中。合并包含单个插入的所得克隆,并且彼此竞争数百代。最后,对最适合的克隆进行了表征,发现其含有与原始DARS2位置非常接近的DARS2。

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