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结核分枝杆菌lipF启动子-10区域的突变分析。

Mutational analysis of the -10 region from the Mycobacterium tuberculosis lipF promoter.

作者信息

Gonzales Michelle, Saviola Beatrice

机构信息

Department of Biological Chemistry, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.

出版信息

Mol Biol Rep. 2009 Jul;36(6):1225-9. doi: 10.1007/s11033-008-9301-9. Epub 2008 Jul 22.

DOI:10.1007/s11033-008-9301-9
PMID:18649013
Abstract

The promoter driving expression of the Mycobacterium tuberculosis gene lipF (Rv3487c) had previously been identified as being upregulated by acidic stress. Subsequently a 59 base pair (bp) acid inducible minimal promoter region was isolated in which a putative -10 region was identified. In this study we use mutational analysis to investigate the -10 region of the lipF promoter. Mutations within this region lead to a dramatic decrease of promoter activity, while a mutation outside of this region does not affect promoter activity.

摘要

此前已确定驱动结核分枝杆菌基因lipF(Rv3487c)表达的启动子受酸性应激上调。随后分离出一个59个碱基对(bp)的酸诱导最小启动子区域,其中鉴定出一个推定的-10区域。在本研究中,我们使用突变分析来研究lipF启动子的-10区域。该区域内的突变导致启动子活性显著降低,而该区域外的突变不影响启动子活性。

相似文献

1
Mutational analysis of the -10 region from the Mycobacterium tuberculosis lipF promoter.结核分枝杆菌lipF启动子-10区域的突变分析。
Mol Biol Rep. 2009 Jul;36(6):1225-9. doi: 10.1007/s11033-008-9301-9. Epub 2008 Jul 22.
2
Determination of the minimal acid-inducible promoter region of the lipF gene from Mycobacterium tuberculosis.结核分枝杆菌lipF基因最小酸诱导启动子区域的测定。
Gene. 2007 Jun 15;395(1-2):22-8. doi: 10.1016/j.gene.2006.12.037. Epub 2007 Jan 20.
3
The lipF promoter of Mycobacterium tuberculosis is upregulated specifically by acidic pH but not by other stress conditions.结核分枝杆菌的lipF启动子在酸性pH条件下特异性上调,而在其他应激条件下则不然。
Microbiol Res. 2009;164(2):228-32. doi: 10.1016/j.micres.2007.06.003. Epub 2007 Sep 14.
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引用本文的文献

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LipF increases rifampicin and streptomycin sensitivity in a Mycobacterium tuberculosis surrogate.脂阿拉伯甘露聚糖(LipF)增加了结核分枝杆菌替代物中利福平与链霉素的敏感性。
BMC Microbiol. 2020 May 25;20(1):132. doi: 10.1186/s12866-020-01802-x.
2
Induction of the acid inducible lipF promoter is reversibly inhibited in pH ranges of pH 4.2-4.0.在pH值为4.2至4.0的范围内,酸诱导型lipF启动子的诱导作用受到可逆抑制。
BMC Res Notes. 2018 May 8;11(1):284. doi: 10.1186/s13104-018-3370-1.

本文引用的文献

1
The lipF promoter of Mycobacterium tuberculosis is upregulated specifically by acidic pH but not by other stress conditions.结核分枝杆菌的lipF启动子在酸性pH条件下特异性上调,而在其他应激条件下则不然。
Microbiol Res. 2009;164(2):228-32. doi: 10.1016/j.micres.2007.06.003. Epub 2007 Sep 14.
2
Determination of the minimal acid-inducible promoter region of the lipF gene from Mycobacterium tuberculosis.结核分枝杆菌lipF基因最小酸诱导启动子区域的测定。
Gene. 2007 Jun 15;395(1-2):22-8. doi: 10.1016/j.gene.2006.12.037. Epub 2007 Jan 20.
3
Expression and characterization of the carboxyl esterase Rv3487c from Mycobacterium tuberculosis.
结核分枝杆菌羧基酯酶Rv3487c的表达与特性分析
Protein Expr Purif. 2005 Jul;42(1):59-66. doi: 10.1016/j.pep.2005.03.022. Epub 2005 Apr 12.
4
Requirement of the mymA operon for appropriate cell wall ultrastructure and persistence of Mycobacterium tuberculosis in the spleens of guinea pigs.耻垢分枝杆菌mymA操纵子对豚鼠脾脏中结核分枝杆菌适当的细胞壁超微结构和持续性的需求。
J Bacteriol. 2005 Jun;187(12):4173-86. doi: 10.1128/JB.187.12.4173-4186.2005.
5
Mutants of Mycobacterium smegmatis unable to grow at acidic pH in the presence of the protonophore carbonyl cyanide m-chlorophenylhydrazone.耻垢分枝杆菌的突变体在质子载体间氯苯腙存在的情况下无法在酸性pH条件下生长。
Microbiology (Reading). 2005 Mar;151(Pt 3):665-672. doi: 10.1099/mic.0.27624-0.
6
Controlling gene expression in mycobacteria with anhydrotetracycline and Tet repressor.利用脱水四环素和四环素阻遏物控制分枝杆菌中的基因表达。
Nucleic Acids Res. 2005 Feb 1;33(2):e21. doi: 10.1093/nar/gni013.
7
Green fluorescent protein is a quantitative reporter of gene expression in individual eukaryotic cells.绿色荧光蛋白是单个真核细胞中基因表达的定量报告分子。
FASEB J. 2005 Mar;19(3):440-2. doi: 10.1096/fj.04-3180fje. Epub 2005 Jan 7.
8
mymA operon of Mycobacterium tuberculosis: its regulation and importance in the cell envelope.结核分枝杆菌的mymA操纵子:其调控及在细胞壁中的重要性
FEMS Microbiol Lett. 2003 Oct 10;227(1):53-63. doi: 10.1016/S0378-1097(03)00648-7.
9
A postgenomic method for predicting essential genes at subsaturation levels of mutagenesis: application to Mycobacterium tuberculosis.一种用于在亚饱和诱变水平下预测必需基因的后基因组方法:应用于结核分枝杆菌。
Proc Natl Acad Sci U S A. 2003 Jun 10;100(12):7213-8. doi: 10.1073/pnas.1231432100. Epub 2003 May 29.
10
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Mol Microbiol. 2003 Apr;48(1):77-84. doi: 10.1046/j.1365-2958.2003.03425.x.