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F因子oriV1区域在不依赖recA的异常重组中的作用。F衍生物pOX38与pBR322相关质粒的稳定复制子融合。

Role of the F factor oriV1 region in recA-independent illegitimate recombination. Stable replicon fusions of the F derivative pOX38 and pBR322-related plasmids.

作者信息

O'Connor M B, Malamy M H

出版信息

J Mol Biol. 1984 May 25;175(3):263-84. doi: 10.1016/0022-2836(84)90348-6.

Abstract

We have used a mating protocol to isolate recA-independent recombinants of pOX38 , an F factor derivative, and the non-conjugative plasmid pMBO311 . Plasmid pMBO311 is a derivative of pBR322 carrying a DNA insertion that contains IS121 and shows no extensive sequence homology to pOX38 . Twenty-seven cointegrate molecules formed during independent mobilizations of pMBO311 by pOX38 were examined by restriction and Southern hybridization analysis. In general, there were two classes of recombinants. A minority class appears to have been mediated by IS121 , resulting in the formation of cointegrate molecules containing IS121 at the junctions between the two plasmids. The majority class (23/27) apparently involved reciprocal recombination between sites on pOX38 and pMBO311 . IS121 does not seem to be responsible for the formation of this type of cointegrate molecule, since similar structures were generated at approximately the same frequency during mobilization of control plasmids that do not contain IS121 . We have localized the regions involved in this second class of recombination events and find that most (17/23) occur at or near oriV1 , the primary replication initiation site of pOX38 . Twelve of the cointegrate molecules showed identical restriction and Southern hybridization patterns demonstrating a preferred region on pMBO311 as well. This site was localized just distal to the tet genes, within a 640-base AvaI-PvuII segment in the pBR322 portion of the molecule.

摘要

我们采用了一种交配方案来分离pOX38(一种F因子衍生物)和非接合性质粒pMBO311的recA非依赖性重组体。质粒pMBO311是pBR322的衍生物,携带一个包含IS121的DNA插入片段,与pOX38没有广泛的序列同源性。通过pOX38对pMBO311进行独立动员过程中形成的27个共整合分子,通过限制性酶切和Southern杂交分析进行了检测。一般来说,有两类重组体。少数类似乎是由IS121介导的,导致在两个质粒的连接处形成含有IS121的共整合分子。多数类(23/27)显然涉及pOX38和pMBO311上位点之间的相互重组。IS121似乎与这类共整合分子的形成无关,因为在不含IS121的对照质粒动员过程中,以大致相同的频率产生了类似的结构。我们已经定位了参与第二类重组事件的区域,发现大多数(17/23)发生在oriV1(pOX38的主要复制起始位点)处或其附近。12个共整合分子显示出相同的限制性酶切和Southern杂交模式,这也证明了pMBO311上有一个优先区域。该位点位于tet基因的远端,在分子pBR322部分的一个640碱基的AvaI - PvuII片段内。

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