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一种大肠杆菌顺式作用抗终止子序列:dnaG 顺反子内转录终止子利用位点

An Escherichia coli cis-acting antiterminator sequence: the dnaG nut site.

作者信息

Almond N, Yajnik V, Svec P, Godson G N

机构信息

Biochemistry Department, NYU Medical Center, NY 10016.

出版信息

Mol Gen Genet. 1989 Apr;216(2-3):195-203. doi: 10.1007/BF00334356.

DOI:10.1007/BF00334356
PMID:2664448
Abstract

The Escherichia coli rpsU-dnaG-rpoD operon contains an internal transcription terminator T1 located in the intergenic region between the rpsU and dnaG genes (Smiley et al. 1982). By cloning T1 as a small 127 bp fragment into the terminator probe plasmid pDR720 between the trp operator promoter and the assayable galK gene, it was shown that T1 acts as a strong transcription terminator, comparable in strength to the 3' operon terminator T2. However, an operon sequence that occurs 5' to T1 within the coding region of the rpsU gene and which has homology with the lambda nut site, (Lupski et al. 1983) when placed 5' to T1 in the pDR720 plasmid construct, modifies transcription through T1 allowing expression of the galK gene. This sequence, called the dnaG nut site also modifies the termination activity of the external operon terminator T2. It is proposed that the dnaG nut site is a cis-acting element of an antitermination system in E. coli.

摘要

大肠杆菌的rpsU - dnaG - rpoD操纵子含有一个位于rpsU基因和dnaG基因之间基因间隔区的内部转录终止子T1(斯迈利等人,1982年)。通过将T1作为一个127 bp的小片段克隆到终止子探针质粒pDR720中,置于色氨酸操纵子启动子和可检测的半乳糖激酶基因之间,结果表明T1作为一个强转录终止子,其强度与3'操纵子终止子T2相当。然而,rpsU基因编码区内T1上游出现的一段操纵子序列,与λ噬菌体的nut位点具有同源性(卢普斯基等人,1983年),当将其置于pDR720质粒构建体中T1的上游时,可改变通过T1的转录,使半乳糖激酶基因得以表达。这个序列,称为dnaG nut位点,也会改变外部操纵子终止子T2的终止活性。有人提出,dnaG nut位点是大肠杆菌中一种抗终止系统的顺式作用元件。

相似文献

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An Escherichia coli cis-acting antiterminator sequence: the dnaG nut site.一种大肠杆菌顺式作用抗终止子序列:dnaG 顺反子内转录终止子利用位点
Mol Gen Genet. 1989 Apr;216(2-3):195-203. doi: 10.1007/BF00334356.
2
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Promotion, termination, and anti-termination in the rpsU-dnaG-rpoD macromolecular synthesis operon of E. coli K-12.大肠杆菌K-12的rpsU-dnaG-rpoD大分子合成操纵子中的促进、终止和抗终止
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引用本文的文献

1
Mutations in the Escherichia coli dnaG gene suggest coupling between DNA replication and chromosome partitioning.大肠杆菌dnaG基因的突变表明DNA复制与染色体分配之间存在偶联关系。
J Bacteriol. 1991 Feb;173(3):1268-78. doi: 10.1128/jb.173.3.1268-1278.1991.
2
Transcription frequency modulates the efficiency of an attenuator preceding the rpoBC RNA polymerase genes of Escherichia coli: possible autogenous control.转录频率调节大肠杆菌RNA聚合酶基因rpoBC之前的弱化子的效率:可能的自体调控。
Nucleic Acids Res. 1992 Sep 25;20(18):4773-9. doi: 10.1093/nar/20.18.4773.

本文引用的文献

1
Termination of transcription and its regulation in the tryptophan operon of E. coli.大肠杆菌色氨酸操纵子中的转录终止及其调控。
Cell. 1981 Apr;24(1):10-23. doi: 10.1016/0092-8674(81)90496-7.
2
Sequences of the Escherichia coli dnaG primase gene and regulation of its expression.大肠杆菌dnaG引发酶基因序列及其表达调控。
Proc Natl Acad Sci U S A. 1982 Aug;79(15):4550-4. doi: 10.1073/pnas.79.15.4550.
3
Effects of promoter strengths and growth conditions on copy number of transcription-fusion vectors.启动子强度和生长条件对转录融合载体拷贝数的影响。
J Biol Chem. 1984 Jun 25;259(12):7399-403.
4
The rpsU-dnaG-rpoD macromolecular synthesis operon of E. coli.大肠杆菌的rpsU-dnaG-rpoD大分子合成操纵子。
Cell. 1984 Dec;39(2 Pt 1):251-2. doi: 10.1016/0092-8674(84)90001-1.
5
Transcription from a heat-inducible promoter causes heat shock regulation of the sigma subunit of E. coli RNA polymerase.来自热诱导启动子的转录导致大肠杆菌RNA聚合酶σ亚基的热休克调节。
Cell. 1984 Sep;38(2):371-81. doi: 10.1016/0092-8674(84)90492-6.
6
Plasmid vectors for the selection of promoters.用于启动子选择的质粒载体。
Gene. 1984 Feb;27(2):151-60. doi: 10.1016/0378-1119(84)90136-7.
7
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.
8
Construction and analysis of in vivo activity of E. coli promoter hybrids and promoter mutants that alter the -35 to -10 spacing.改变-35至-10间距的大肠杆菌启动子杂种和启动子突变体的体内活性构建与分析。
Gene. 1982 Dec;20(2):231-43. doi: 10.1016/0378-1119(82)90042-7.
9
Synthesis of the nutL DNA segments and analysis of antitermination and termination functions in coliphage lambda.大肠杆菌噬菌体λ中nutL DNA片段的合成及抗终止和终止功能分析。
Gene. 1982 Jun;18(3):343-54. doi: 10.1016/0378-1119(82)90173-1.
10
Cloning and characterization of the Escherichia coli chromosomal region surrounding the dnaG Gene, with a correlated physical and genetic map of dnaG generated via transposon Tn5 mutagenesis.大肠杆菌dnaG基因周围染色体区域的克隆与特性分析,以及通过转座子Tn5诱变产生的dnaG相关物理图谱和遗传图谱。
Mol Gen Genet. 1982;185(1):120-8. doi: 10.1007/BF00333800.