Panayotatos N
Nucleic Acids Res. 1984 Mar 26;12(6):2641-8. doi: 10.1093/nar/12.6.2641.
ColE1 derivative plasmids were constructed in which the natural promoter that primes replication or, in addition, the region coding for the RNA I control element had been deleted. In all of these molecules priming of the origin was effected by read-through transcription from constitutive or inducible (lacUV5) promoters inserted farther upstream. In the latter case, regulation of lac repressor activity with IPTG resulted in controlled plasmid levels in vivo. These results indicated that, at least in the absence of other control elements, regulation of the priming promoter was sufficient to control DNA replication and determine plasmid copy number.
构建了ColE1衍生质粒,其中引发复制的天然启动子或此外编码RNA I控制元件的区域已被删除。在所有这些分子中,起始点的引发是通过从插入更上游的组成型或诱导型(lacUV5)启动子的通读转录来实现的。在后一种情况下,用IPTG调节lac阻遏物活性导致体内质粒水平受到控制。这些结果表明,至少在没有其他控制元件的情况下,引发启动子的调节足以控制DNA复制并确定质粒拷贝数。