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RepA(一种必需的复制蛋白)与质粒P307的RepFIB的DNA重复序列之间的调控相互作用。

Regulatory interactions between RepA, an essential replication protein, and the DNA repeats of RepFIB from plasmid P307.

作者信息

Spiers A J, Bhana N, Bergquist P L

机构信息

Centre for Gene Technology, University of Auckland, New Zealand.

出版信息

J Bacteriol. 1993 Jul;175(13):4016-24. doi: 10.1128/jb.175.13.4016-4024.1993.

DOI:10.1128/jb.175.13.4016-4024.1993
PMID:8320218
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC204830/
Abstract

The control of RepFIB replication appears to rely on the interaction between an initiator protein (RepA) and two sets of DNA repeat elements located on either side of the repA gene (BCDD'D" and EFGHIJ). In vivo genetic tests demonstrate that the BCDD'D" repeats form part of the origin of replication, while some of the downstream repeat elements (HIJ) are involved in the sensing and setting of plasmid copy number. RepA DNA binding to these groups of repeats has been investigated in vivo by utilizing the fact that the replicon contains three active promoters (orip, repAp, and EFp), one of which has previously been shown to control the expression of repA (repAp). All three promoters are closely associated with the repeat elements flanking repA, and an investigation using lacZ or cml gene fusions has demonstrated that RepA expressed in trans is able to repress each promoter. However, these assays suggest that the transcriptional responses of orip and repAp to RepA repression are significantly different, despite the fact that both promoters are embedded within the BCDD'D" repeat elements. Extra copies of the BCDD'D" or EFG repeats in trans have no effect on RepA repression of repAp embedded in a second copy of the BCDD'D" repeats, but copies of the HIJ or EFGHIJ repeats are able to derepress repAp, suggesting that there is a fundamental difference between RepA-BCDD'D" or -HIJ complexes and RepA-EFG or -EFGHIJ complexes.

摘要

RepFIB复制的控制似乎依赖于一种起始蛋白(RepA)与位于repA基因两侧的两组DNA重复元件(BCDD'D"和EFGHIJ)之间的相互作用。体内遗传学测试表明,BCDD'D"重复序列构成了复制起点的一部分,而一些下游重复元件(HIJ)则参与了质粒拷贝数的感知和设定。利用复制子包含三个活性启动子(orip、repAp和EFp)这一事实,在体内研究了RepA与这些重复序列组的DNA结合情况,其中一个启动子先前已被证明可控制repA的表达(repAp)。所有三个启动子都与repA侧翼的重复元件紧密相关,使用lacZ或cml基因融合的研究表明,反式表达的RepA能够抑制每个启动子。然而,这些分析表明,尽管orip和repAp都嵌入在BCDD'D"重复元件中,但它们对RepA抑制的转录反应却显著不同。反式存在的BCDD'D"或EFG重复序列的额外拷贝对嵌入在第二个BCDD'D"重复序列拷贝中的repAp的RepA抑制没有影响,但HIJ或EFGHIJ重复序列的拷贝能够解除对repAp的抑制,这表明RepA-BCDD'D"或-HIJ复合物与RepA-EFG或-EFGHIJ复合物之间存在根本差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9549/204830/e0aeb2cf3225/jbacter00055-0115-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9549/204830/e0aeb2cf3225/jbacter00055-0115-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9549/204830/e0aeb2cf3225/jbacter00055-0115-a.jpg

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