Suppr超能文献

大肠杆菌整合宿主因子可逆转π起始蛋白对R6K质粒复制的抑制作用。

Integration host factor of Escherichia coli reverses the inhibition of R6K plasmid replication by pi initiator protein.

作者信息

Dellis S, Filutowicz M

机构信息

Department of Bacteriology, University of Wisconsin-Madison 53706.

出版信息

J Bacteriol. 1991 Feb;173(3):1279-86. doi: 10.1128/jb.173.3.1279-1286.1991.

Abstract

Integration host factor (IHF) protein is the only host-encoded protein known to bind and to affect replication of the gamma origin of Escherichia coli plasmid R6K. We examined the ability of R6K origins to replicate in cells lacking either of the two subunits of IHF. As shown previously, the gamma origin cannot replicate in IHF-deficient cells. However, this inability to replicate was relieved under the following conditions: underproduction of the wild-type pi replication protein of R6K or production of normal levels of mutant pi proteins which exhibit relaxed replication control. The copy number of plasmids containing the primary R6K origins (alpha and beta) is substantially reduced in IHF-deficient bacteria. Furthermore, replication of these plasmids is completely inhibited if the IHF-deficient strains contain a helper plasmid producing additional wild-type pi protein. IHF protein has previously been shown to bind to two sites within the gamma origin. These sites flank a central repeat segment which binds pi protein. We propose a model in which IHF binding to its sites reduces the replication inhibitor activity of pi protein at all three R6K origins.

摘要

整合宿主因子(IHF)蛋白是已知的唯一一种能结合并影响大肠杆菌质粒R6Kγ 型复制起点复制的宿主编码蛋白。我们研究了R6K复制起点在缺乏IHF两个亚基之一的细胞中的复制能力。如先前所示,γ 型复制起点在缺乏IHF的细胞中无法复制。然而,在以下条件下这种无法复制的情况得到了缓解:R6K野生型π 复制蛋白产量不足,或产生正常水平的表现出松弛复制控制的突变型π 蛋白。在缺乏IHF的细菌中,含有R6K主要复制起点(α 和β)的质粒拷贝数大幅减少。此外,如果缺乏IHF的菌株含有产生额外野生型π 蛋白的辅助质粒,这些质粒的复制会被完全抑制。先前已证明IHF蛋白能结合γ 型复制起点内的两个位点。这些位点位于一个结合π 蛋白的中央重复片段两侧。我们提出了一个模型,其中IHF与其位点的结合降低了π 蛋白在所有三个R6K复制起点处的复制抑制活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41bf/207252/a7e9f353dbc6/jbacter00093-0355-a.jpg

相似文献

4
8
Negative control of plasmid R6K replication: possible role of intermolecular coupling of replication origins.
Proc Natl Acad Sci U S A. 1989 Oct;86(20):7942-6. doi: 10.1073/pnas.86.20.7942.
10
Investigations of pi initiator protein-mediated interaction between replication origins alpha and gamma of the plasmid R6K.
J Biol Chem. 2010 Feb 19;285(8):5695-704. doi: 10.1074/jbc.M109.067439. Epub 2009 Dec 22.

引用本文的文献

1
Two replication regions in the pJM1 virulence plasmid of the marine pathogen Vibrio anguillarum.
Plasmid. 2012 Mar;67(2):95-101. doi: 10.1016/j.plasmid.2011.12.008. Epub 2012 Jan 4.
2
pi protein- and ATP-dependent transitions from 'closed' to 'open' complexes at the gamma ori of plasmid R6K.
Nucleic Acids Res. 2003 Oct 15;31(20):5993-6003. doi: 10.1093/nar/gkg809.
4
Replication and control of circular bacterial plasmids.
Microbiol Mol Biol Rev. 1998 Jun;62(2):434-64. doi: 10.1128/MMBR.62.2.434-464.1998.
9
A DNA segment conferring stable maintenance on R6K gamma-origin core replicons.
J Bacteriol. 1995 Nov;177(22):6338-45. doi: 10.1128/jb.177.22.6338-6345.1995.
10
Roles of a 106-bp origin enhancer and Escherichia coli DnaA protein in replication of plasmid R6K.
Nucleic Acids Res. 1992 Feb 25;20(4):811-7. doi: 10.1093/nar/20.4.811.

本文引用的文献

2
Plasmid R6K DNA replication. I. Complete nucleotide sequence of an autonomously replicating segment.
J Mol Biol. 1982 Oct 15;161(1):33-43. doi: 10.1016/0022-2836(82)90276-5.
3
int-h: An int mutation of phage lambda that enhances site-specific recombination.
Cell. 1980 Jul;20(3):721-9. doi: 10.1016/0092-8674(80)90318-9.
5
Release of initiation control by a mutational alteration in the R6K pi protein required for plasmid DNA replication.
Proc Natl Acad Sci U S A. 1983 Sep;80(18):5500-4. doi: 10.1073/pnas.80.18.5500.
7
Direct role of the himA gene product in phage lambda integration.
Nature. 1981 Apr 9;290(5806):523-6. doi: 10.1038/290523a0.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验