Løbner-Olesen A, von Freiesleben U
University of Colorado at Boulder, Dept of Molecular Cellular and Developmental Biology 80309, USA.
EMBO J. 1996 Nov 1;15(21):5999-6008.
Dam methyltransferase deficient Escherichia coli cells containing minichromosomes were constructed. Free plasmid DNA could not be detected in these cells and the minichromosomes were found to be integrated in multiple copies in the origin of replication (oriC) region of the host chromosome. The absence of the initiation cascade in Dam- cells is proposed to account for this observation of apparent incompatibility between plasmid and chromosomal copies of oriC. Studies using oriC-pBR322 chimeric plasmids and their deletion derivatives indicated that the incompatibility determinant is an intact and functional oriC sequence. The seqA2 mutation was found to overcome the incompatability phenotype by increasing the cellular oriC copy number 3-fold thereby allowing minichromosomes to coexist with the chromosome. The replication pattern of a wild-type strain with multiple integrated minichromosomes in the oriC region of the chromosome, led to the conclusion that initiation of DNA replication commences at a fixed cell mass, irrespective of the number of origins contained on the chromosome.
构建了含有微型染色体的Dam甲基转移酶缺陷型大肠杆菌细胞。在这些细胞中未检测到游离的质粒DNA,并且发现微型染色体以多拷贝形式整合在宿主染色体的复制起点(oriC)区域。有人提出,Dam -细胞中起始级联反应的缺失可以解释oriC的质粒拷贝和染色体拷贝之间明显不相容的这一现象。使用oriC - pBR322嵌合质粒及其缺失衍生物的研究表明,不相容决定因素是完整且功能正常的oriC序列。发现seqA2突变通过将细胞oriC拷贝数增加3倍来克服不相容表型,从而使微型染色体能够与染色体共存。在染色体oriC区域具有多个整合微型染色体的野生型菌株的复制模式,得出了DNA复制起始于固定细胞量的结论,而与染色体上所含的起始点数量无关。