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大肠杆菌K-12中uxuR调控基因表达涉及多种调控。

Multiple regulation involved in the expression of the uxuR regulatory gene in Escherichia coli K-12.

作者信息

Ritzenthaler P, Mata-Gilsinger M

出版信息

Mol Gen Genet. 1983;189(2):351-4. doi: 10.1007/BF00337831.

DOI:10.1007/BF00337831
PMID:6406797
Abstract

We have isolated a strain carrying a fusion of the beta-galactosidase structural gene to the promoter of the uxuR regulatory gene with the aid of the Casadaban Mud (Aprlac) phage. Analysis of mutants with deletions that were derived from the uxuR::Mud1 insertion strain confirmed the counterclockwise transcription direction of the uxuR gene. The uxuR-lacZ fusion strain was also used to examine the regulation of expression from the uxuR promoter. It was observed that an increase in the copy number of the uxuR gene results in an increased repression of beta-galactosidase synthesis. Overproduction of the exuR repressor also caused a decrease of the beta-galactosidase level. In all cases, the repression of beta-galactosidase synthesis was accompanied by a stronger repression of uxuB gene product synthesis. These results indicate that the expression of the uxuR gene is repressed by its own product but also by the exuR repressor. The different types of regulation of the two uxu operons are thus identical.

摘要

我们借助卡萨达班 Mud(Aprlac)噬菌体分离出了一个菌株,该菌株携带β-半乳糖苷酶结构基因与uxuR 调控基因启动子的融合基因。对源自 uxuR::Mud1 插入菌株的缺失突变体进行分析,证实了 uxuR 基因的逆时针转录方向。uxuR-lacZ 融合菌株也被用于检测 uxuR 启动子的表达调控。观察到 uxuR 基因拷贝数的增加导致β-半乳糖苷酶合成的抑制增强。exuR 阻遏物的过量产生也导致β-半乳糖苷酶水平降低。在所有情况下,β-半乳糖苷酶合成的抑制都伴随着 uxuB 基因产物合成的更强抑制。这些结果表明,uxuR 基因的表达不仅受到其自身产物的抑制,也受到 exuR 阻遏物的抑制。因此,两个 uxu 操纵子的不同调控类型是相同的。

相似文献

1
Multiple regulation involved in the expression of the uxuR regulatory gene in Escherichia coli K-12.大肠杆菌K-12中uxuR调控基因表达涉及多种调控。
Mol Gen Genet. 1983;189(2):351-4. doi: 10.1007/BF00337831.
2
Regulation of expression of the uxu operon and of the uxuR regulatory gene in Escherichia coli K12.大肠杆菌K12中uxu操纵子及uxuR调控基因表达的调控
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Interchangeability of repressors for the control of the uxu and uid operons in E. coli K12.大肠杆菌K12中阻遏物对uxu和uid操纵子控制的互换性。
Mol Gen Genet. 1983;191(2):263-70. doi: 10.1007/BF00334824.
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Use of in vitro gene fusions to study the uxuR regulatory gene in Escherichia coli K-12: direction of transcription and regulation of its expression.利用体外基因融合技术研究大肠杆菌K-12中的uxuR调控基因:转录方向及其表达调控
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Control of hexuronate metabolism in Escherichia coli by the two interdependent regulators, ExuR and UxuR: derepression by heterodimer formation.大肠杆菌中由两个相互依赖的调节因子ExuR和UxuR对己糖醛酸代谢的调控:通过异源二聚体形成实现去阻遏
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Isolation of a functional exuR-repressor-beta-galactosidase hybrid protein by use of in vitro gene fusions.利用体外基因融合技术分离功能性exuR阻遏蛋白-β-半乳糖苷酶杂合蛋白。
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引用本文的文献

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Deciphering allosterism of an hexuronate metabolism regulator: UxuR.解析己糖醛酸代谢调节剂UxuR的变构作用
RSC Med Chem. 2025 Jun 30. doi: 10.1039/d5md00391a.
2
Differential Impact of Hexuronate Regulators ExuR and UxuR on the Proteome.Hexuronate 调节剂 ExuR 和 UxuR 对蛋白质组的差异影响。
Int J Mol Sci. 2022 Jul 29;23(15):8379. doi: 10.3390/ijms23158379.
3
GntP is the Escherichia coli Fructuronic acid transporter and belongs to the UxuR regulon.GntP是大肠杆菌的果糖醛酸转运蛋白,属于UxuR调控子。

本文引用的文献

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Trp aporepressor production is controlled by autogenous regulation and inefficient translation.色氨酸阻遏物的产生受自身调节和低效翻译的控制。
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Regulation of hexuronate system genes in Escherichia coli K-12: multiple regulation of the uxu operon by exuR and uxuR gene products.大肠杆菌K-12中己糖醛酸系统基因的调控:exuR和uxuR基因产物对uxu操纵子的多重调控
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Interchangeability of repressors for the control of the uxu and uid operons in E. coli K12.大肠杆菌K12中阻遏物对uxu和uid操纵子控制的互换性。
Mol Gen Genet. 1983;191(2):263-70. doi: 10.1007/BF00334824.
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Genetic analysis of uxuR and exuR genes: evidence for ExuR and UxuR monomer repressors interactions.uxuR和exuR基因的遗传分析:ExuR和UxuR单体阻遏物相互作用的证据
Mol Gen Genet. 1985;199(3):507-11. doi: 10.1007/BF00330766.
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The lexA gene product represses its own promoter.lexA基因产物可抑制其自身的启动子。
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Molecular cloning of Escherichia coli K-12 hexuronate system genes: exu region.大肠杆菌K-12己糖醛酸系统基因的分子克隆:exu区域
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Use of in vitro gene fusions to study the uxuR regulatory gene in Escherichia coli K-12: direction of transcription and regulation of its expression.利用体外基因融合技术研究大肠杆菌K-12中的uxuR调控基因:转录方向及其表达调控
J Bacteriol. 1982 Jun;150(3):1040-7. doi: 10.1128/jb.150.3.1040-1047.1982.
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Cloning and endonuclease restriction analysis of uidA and uidR genes in Escherichia coli K-12: determination of transcription direction for the uidA gene.大肠杆菌K-12中uidA和uidR基因的克隆及核酸内切酶限制分析:uidA基因转录方向的确定
J Bacteriol. 1982 Feb;149(2):587-94. doi: 10.1128/jb.149.2.587-594.1982.
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Use of bacteriophage transposon Mu d1 to determine the orientation for three proC-linked phosphate-starvation-inducible (psi) genes in Escherichia coli K-12.利用噬菌体转座子Mu d1确定大肠杆菌K-12中三个与proC相连的磷酸盐饥饿诱导(psi)基因的方向。
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