The arginine regulon of Escherichia coli:: whole-system transcriptome analysis discovers new genes and provides an integrated view of arginine regulation

被引:61
作者
Caldara, Marina [1 ]
Charlier, Daniel [1 ]
Cunin, Raymond [1 ]
机构
[1] Vrije Univ Brussel, Lab Erfelijkheidsleer & Microbiol, B-1050 Brussels, Belgium
来源
MICROBIOLOGY-SGM | 2006年 / 152卷
关键词
D O I
10.1099/mic.0.29088-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Analysis of the response to arginine of the Escherichia coli K-12 transcriptome by microarray hybridization and real-time quantitative PCR provides the first coherent quantitative picture of the ArgR-mediated repression of arginine biosynthesis and uptake genes. Transcriptional repression was shown to be the major control mechanism of the biosynthetic genes, leaving only limited room for additional transcriptional or post-transcriptional regulation. The art genes, encoding the specific arginine uptake system, are subject to ArgR-mediated repression, with strong repression of artJ, encoding the periplasmic binding protein of the system. The hisJQMP genes of the histidine transporter (part of the lysine-arginine-ornithine uptake system) were discovered to be a part of the arginine regulon. Analysis of their control region with reporter gene fusions and electrophoretic mobility shift in the presence of pure ArgR repressor showed the involvement in repression of the ArgR protein and an ARG box 120 bp upstream of hisJ. No repression of the genes of the third uptake system, arginine-ornithine, was observed. Finally, comparison of the time course of arginine repression of gene transcription with the evolution of the specific activities of the cognate enzymes showed that while full genetic repression was achieved 2 min after arginine addition, enzyme concentrations were diluted at the rate of cell division. This emphasizes the importance of feedback inhibition of the first enzymic step in the pathway in controlling the metabolic flow through biosynthesis in the period following the onset of repression.
引用
收藏
页码:3343 / 3354
页数:12
相关论文
共 50 条
[1]   A new yeast metabolon involving at least the two first enzymes of arginine biosynthesis - Acetylglutamate synthase activity requires complex formation with acetylglutamate kinase [J].
Abadjieva, A ;
Pauwels, K ;
Hilven, P ;
Crabeel, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (46) :42869-42880
[3]  
Bachmann B.J., 1987, ESCHERICHIA COLI SAL, P1190
[4]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[5]   TRANSCRIPTION OF REGIONS WITHIN THE DIVERGENT ARGECBH OPERON OF ESCHERICHIA-COLI - EVIDENCE FOR LACK OF AN ATTENUATION MECHANISM [J].
BENY, G ;
CUNIN, R ;
GLANSDORFF, N ;
BOYEN, A ;
CHARLIER, J ;
KELKER, N .
JOURNAL OF BACTERIOLOGY, 1982, 151 (01) :58-61
[6]   QUANTIFYING THE ALLOSTERIC PROPERTIES OF ESCHERICHIA-COLI CARBAMYL-PHOSPHATE SYNTHETASE - DETERMINATION OF THERMODYNAMIC LINKED-FUNCTION PARAMETERS IN AN ORDERED KINETIC MECHANISM [J].
BRAXTON, BL ;
MULLINS, LS ;
RAUSHEL, FM ;
REINHART, GD .
BIOCHEMISTRY, 1992, 31 (08) :2309-2316
[7]  
CALDARA M, 2005, SYSTEMS BIOL MOL MOD, P145
[8]   Phosphorylation of the periplasmic binding protein in two transport systems for arginine incorporation in Escherichia coli K-12 is unrelated to the function of the transport system [J].
Celis, RTF ;
Leadlay, PF ;
Roy, I ;
Hansen, A .
JOURNAL OF BACTERIOLOGY, 1998, 180 (18) :4828-4833
[9]   Repression and activation of arginine transport genes in Escherichia coli K 12 by the ArgP protein [J].
Celis, RTF .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 294 (05) :1087-1095
[10]   PROPERTIES OF AN ESCHERICHIA-COLI K-12 MUTANT DEFECTIVE IN TRANSPORT OF ARGININE AND ORNITHINE [J].
CELIS, TFR .
JOURNAL OF BACTERIOLOGY, 1977, 130 (03) :1234-1243