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关于一种阻遏物存在的遗传学证据,该阻遏物可调节质粒ColD-CA23上大肠杆菌素D的表达。

Genetic evidence for the existence of a repressor that modulates colicin D expression on plasmid ColD-CA23.

作者信息

Ghersa P, Lurz R, Dobrinski B, Deshusses J, Belet M, Frey J

机构信息

Département de Biochimie, Université de Genève, Switzerland.

出版信息

Mol Gen Genet. 1988 Jul;213(1):36-41. doi: 10.1007/BF00333395.

DOI:10.1007/BF00333395
PMID:2851708
Abstract

The plasmid ColD-CA23, a high copy number plasmid of 5.12 kb, contains genes for colicin D (cda), for immunity colicin D (cdi), and for a lysis function (cdl). These genes are arranged on a contiguous 2.4 kb fragment in the following sequence: cda, cdi, cdl. They are transcribed in two operons, one transcribing cda and cdl from a SOS inducible promoter, the other transcribing cdi in the opposite direction. The expression of cda and cdl is modulated by a repressor, cdr, which is encoded on the same transcript as cda and cdl. In the absence of this repressor, transcription from the SOS inducible colicin D promoter is exceptionally strong and leads to protein contents up to 50% of total cellular proteins. This autoregulative repressor is a new finding in the control mechanisms of expression of colicins. We have also identified the gene product of cdl to be a 10,000 dalton protein.

摘要

质粒ColD-CA23是一个5.12 kb的高拷贝数质粒,含有大肠杆菌素D(cda)、大肠杆菌素D免疫蛋白(cdi)以及裂解功能蛋白(cdl)的基因。这些基因以cda、cdi、cdl的顺序排列在一个连续的2.4 kb片段上。它们由两个操纵子转录,一个从SOS诱导型启动子转录cda和cdl,另一个以相反方向转录cdi。cda和cdl的表达受阻遏物cdr调控,cdr与cda和cdl在同一转录本上编码。在没有这种阻遏物的情况下,来自SOS诱导型大肠杆菌素D启动子的转录异常强烈,导致蛋白质含量高达细胞总蛋白的50%。这种自动调节阻遏物是大肠杆菌素表达控制机制中的一个新发现。我们还确定cdl的基因产物是一种10,000道尔顿的蛋白质。

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Genetic evidence for the existence of a repressor that modulates colicin D expression on plasmid ColD-CA23.关于一种阻遏物存在的遗传学证据,该阻遏物可调节质粒ColD-CA23上大肠杆菌素D的表达。
Mol Gen Genet. 1988 Jul;213(1):36-41. doi: 10.1007/BF00333395.
2
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引用本文的文献

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Construction of a ColD cda promoter-based SOS-green fluorescent protein whole-cell biosensor with higher sensitivity toward genotoxic compounds than constructs based on recA, umuDC, or sulA promoters.构建一种基于ColD cda启动子的SOS-绿色荧光蛋白全细胞生物传感器,该传感器对遗传毒性化合物的敏感性高于基于recA、umuDC或sulA启动子构建的传感器。
Appl Environ Microbiol. 2005 May;71(5):2338-46. doi: 10.1128/AEM.71.5.2338-2346.2005.

本文引用的文献

1
Plasmid replication functions. VII. Electron microscopic localization of RNA polymerase binding sites in the replication control region of plasmid R6-5.质粒复制功能。VII. 质粒R6 - 5复制控制区域中RNA聚合酶结合位点的电子显微镜定位
Mol Gen Genet. 1981;183(3):490-6. doi: 10.1007/BF00268770.
2
Electron microscopic studies of the binding of Escherichia coli RNA polymerase to DNA. II. Formation of multiple promoter-like complexes at non-promoter sites.大肠杆菌RNA聚合酶与DNA结合的电子显微镜研究。II. 在非启动子位点形成多个类似启动子的复合物。
J Mol Biol. 1980 Jan 5;136(1):79-93. doi: 10.1016/0022-2836(80)90367-8.
3
Transcription regulation of colicin Ib synthesis.
大肠杆菌素Ib合成的转录调控
Mol Gen Genet. 1981;183(3):522-7. doi: 10.1007/BF00268775.
4
The use of transposon Tn5 mutagenesis in the rapid generation of correlated physical and genetic maps of DNA segments cloned into multicopy plasmids--a review.转座子Tn5诱变技术在快速构建克隆于多拷贝质粒的DNA片段的相关物理图谱和遗传图谱中的应用——综述
Gene. 1984 Feb;27(2):131-49. doi: 10.1016/0378-1119(84)90135-5.
5
In vitro insertional mutagenesis with a selectable DNA fragment.利用可选择的DNA片段进行体外插入诱变。
Gene. 1984 Sep;29(3):303-13. doi: 10.1016/0378-1119(84)90059-3.
6
Visual biochemistry: new insight into structure and function of the genome.
Methods Biochem Anal. 1982;28:201-65. doi: 10.1002/9780470110485.ch5.
7
Inhibition of ColE1 RNA primer formation by a plasmid-specified small RNA.一种质粒特异性小RNA对ColE1 RNA引物形成的抑制作用。
Proc Natl Acad Sci U S A. 1981 Mar;78(3):1421-5. doi: 10.1073/pnas.78.3.1421.
8
The killing of sensitive cells by colicin D.大肠杆菌素D对敏感细胞的杀伤作用。
Biochim Biophys Acta. 1972 Mar 14;262(2):200-7. doi: 10.1016/0005-2787(72)90233-x.
9
Two major groups of colicin factors: their evolutionary significance.大肠杆菌素因子的两大主要类别:它们的进化意义
Mol Gen Genet. 1973 Sep 12;125(3):217-30. doi: 10.1007/BF00270744.
10
Pedigrees of some mutant strains of Escherichia coli K-12.大肠杆菌K-12某些突变菌株的谱系。
Bacteriol Rev. 1972 Dec;36(4):525-57. doi: 10.1128/br.36.4.525-557.1972.