Nordheim A, Hashimoto-Gotoh T, Timmis K N
J Bacteriol. 1980 Dec;144(3):923-32. doi: 10.1128/jb.144.3.923-932.1980.
A nick-labeling method has been used to localize the relaxation complex nick sites in three plasmids (pSC101, RSF1010, and R6K) that differ markedly in their host range, deoxyribonucleic acid replication, and conjugal transfer properties. Single specific relaxation sites were located in pSC101 and RSF1010, but surprisingly two distinct sites could be identified in the bi-origin plasmid R6K. In all cases, relaxation nick sites, which are thought to be origins of plasmid conjugal transfer, were shown to be located near origins of vegetative replication. This result suggests a functional interaction between these two types of deoxyribonucleic acid loci, and we speculate here that application events initiated at origins of replication may constitute an integral part of the process of conjugal transfer of small plasmids among bacteria. Consistent with this proposal is the finding that inhibition of vegetative replication of the pSC101 and ColE1 plasmids results in a severe inhibition of their conjugal transfer ability.
一种缺口标记方法已被用于定位三种质粒(pSC101、RSF1010和R6K)中的松弛复合体缺口位点,这三种质粒在宿主范围、脱氧核糖核酸复制和接合转移特性方面有显著差异。在pSC101和RSF1010中定位到了单个特定的松弛位点,但令人惊讶的是,在双原点质粒R6K中可以鉴定出两个不同的位点。在所有情况下,被认为是质粒接合转移起源的松弛缺口位点都位于营养复制起点附近。这一结果表明这两种类型的脱氧核糖核酸位点之间存在功能相互作用,我们在此推测,在复制起点启动的应用事件可能构成细菌中小质粒接合转移过程的一个组成部分。与这一观点一致的是,pSC101和ColE1质粒的营养复制受到抑制会导致它们的接合转移能力严重受损。