Iordanescu S
Department of Plasmid Biology, Public Health Research Institute, New York, NY 10016.
Mol Gen Genet. 1989 Jun;217(2-3):481-7. doi: 10.1007/BF02464921.
pT181 and pC221 are closely related Staphylococcus aureus plasmids with the same genome organization, which is characterized by the overlapping of the origin of replication with the sequence encoding a protein, Rep, essential for plasmid replication. Former results have shown the lack of in vivo cross-complementation between these two plasmids, while in vitro studies have revealed the ability of both Rep proteins to act on either origin. One possible explanation for this difference was based on a previous analysis of the incompatibility expressed by the origin of replication of these plasmids, showing that the origin embedded in the rep gene competes for Rep utilization with the origin of a test plasmid and that changes in the sequence of the origin reduce its ability to compete. To avoid this problem, in the present work special hybrids were constructed in which the origin of replication overlapping the rep gene was mutationally inactivated, without changing the amino acid sequence of the encoded protein. The level of Rep expression by these hybrids could be varied by taking advantage of what is presently known about the control of Rep synthesis in plasmid pT181.(ABSTRACT TRUNCATED AT 250 WORDS)
pT181和pC221是密切相关的金黄色葡萄球菌质粒,具有相同的基因组组织,其特征是复制起点与编码质粒复制所必需的蛋白质Rep的序列重叠。先前的研究结果表明这两种质粒在体内缺乏交叉互补,而体外研究显示两种Rep蛋白都能够作用于任一复制起点。这种差异的一种可能解释基于对这些质粒复制起点所表现出的不相容性的先前分析,结果表明嵌入rep基因中的复制起点与测试质粒的复制起点竞争Rep的利用,并且复制起点序列的改变会降低其竞争能力。为避免这个问题,在本研究中构建了特殊的杂种质粒,其中与rep基因重叠的复制起点经突变失活,而不改变所编码蛋白质的氨基酸序列。利用目前已知的质粒pT181中Rep合成的控制机制,这些杂种质粒的Rep表达水平可以改变。(摘要截短于250字)