首页> 美国卫生研究院文献>The EMBO Journal >A single amino acid alteration in the initiation protein is responsible for the DNA overproduction phenotype of copy number mutants of plasmid R6K.
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A single amino acid alteration in the initiation protein is responsible for the DNA overproduction phenotype of copy number mutants of plasmid R6K.

机译:起始蛋白中的单个氨基酸改变是造成质粒R6K拷贝数突变体的DNA生产过剩的表型。

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摘要

A novel type of high copy-number (cop) mutants of a mini-R6K plasmid were isolated. The mutations were mapped in the pir gene which encodes the pi initiation protein for plasmid R6K DNA replication. They resulted in an alteration by substitution of a single amino acid: threonine to isoleucine at the 108th position for the cop41, and proline to serine at the 113th position for the cop50, of the 305 amino acid pi protein. The cop41 mutation in the pi protein was found to be trans-dominant over the wild-type allele in the copy control of plasmid R6K. Moreover, it was shown that the altered pi protein was not overproduced in maxicells carrying this mutant plasmid and had a higher affinity to the repeated sequence which is present in the pir promoter region. Most likely the mutated pi protein also interacts more efficiently with the same repeated sequences, a target of pi, in the replication origin region and increases the frequency of the initiation event per cell division.
机译:分离出一种新型的mini-R6K质粒的高拷贝数(cop)突变体。突变定位在编码质粒R6K DNA复制的pi起始蛋白的pir基因中。他们通过将单个氨基酸替换为改变:cop41在第108位的苏氨酸替换为异亮氨酸,在305个氨基酸pi蛋白的cop50替换在113位的脯氨酸脯氨酸。在质粒R6K的复制对照中,发现pi蛋白中的cop41突变在野生型等位基因上是反型的。此外,已表明,在携带该突变质粒的极大片段中,改变的π蛋白不会过量产生,并且对存在于pir启动子区域的重复序列具有更高的亲和力。最有可能的是,突变的pi蛋白还可以在复制起点区域中与pi的靶标相同的重复序列更有效地相互作用,并增加每个细胞分裂的起始事件的频率。

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