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携带大肠杆菌染色体复制起点的质粒的拷贝数突变体:复制控制区的证据。

Copy-number mutants of the plasmid carrying the replication origin of the Escherichia coli chromosome: evidence for a control region of replication.

作者信息

Ogura T, Miki T, Hiraga S

出版信息

Proc Natl Acad Sci U S A. 1980 Jul;77(7):3993-7. doi: 10.1073/pnas.77.7.3993.

Abstract

A composite plasmid (pXX11) was constructed by joining of an oriC plasmid (pMCR115) carrying the replication origin (oriC) of the Escherichia coli chromosome and a mini-F plasmid (pSC138) carrying the ampicillin-resistance gene (bla). Plasmid pXX11 can replicate, by using oriC, in Hfr cells and mafA mutant cells that cannot support replication of an F plasmid. This plasmid is stably maintained in these host cells during cell growth even under nonselective conditions by use of the partition mechanism of the mini-F genome. In contrast to other oriC plasmids reported previously, pXX11 has no detectable effect on host cell growth. Higher copy-number (Cop-) mutants of pXX11 were isolated, and some of them were found to carry an insertion or deletion within a region derived from the E. coli chromosome. This region, designated cop (copy number), covers about 0.7 kilobase pair and is located approximately 3 kilobase pairs away from the oriC region at the side opposite the asn gene. Evidence suggests that the normal cop region locted on the oriC plasmid acts to reduce the copy number of the plasmid. Plasmid pXX11 complements the uncB402 mutation located on the host chromosome, but some of the Cop- plasmids do not, suggesting that the cop region is vey closely linked to uncB.

摘要

通过连接携带大肠杆菌染色体复制起点(oriC)的oriC质粒(pMCR115)和携带氨苄青霉素抗性基因(bla)的mini-F质粒(pSC138)构建了复合质粒(pXX11)。质粒pXX11可利用oriC在不能支持F质粒复制的高频重组(Hfr)细胞和mafA突变细胞中复制。通过利用mini-F基因组的分配机制,即使在非选择性条件下,该质粒在细胞生长过程中也能在这些宿主细胞中稳定维持。与先前报道的其他oriC质粒不同,pXX11对宿主细胞生长没有可检测到的影响。分离出了pXX11的高拷贝数(Cop-)突变体,发现其中一些在源自大肠杆菌染色体的区域内有插入或缺失。该区域被命名为cop(拷贝数),覆盖约0.7千碱基对,位于oriC区域与天冬酰胺基因相对一侧约3千碱基对处。有证据表明,位于oriC质粒上的正常cop区域起到降低质粒拷贝数的作用。质粒pXX11可互补位于宿主染色体上的uncB402突变,但一些Cop-质粒不能,这表明cop区域与uncB紧密连锁。

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