This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental material
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kang, Y.
Right arrow Articles by Blattner, F. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kang, Y.
Right arrow Articles by Blattner, F. R.
Right arrowPubmed/NCBI databases
*Gene*GEO Profiles
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*OXYGEN

 Previous Article  |  Next Article 

Journal of Bacteriology, February 2005, p. 1135-1160, Vol. 187, No. 3
0021-9193/05/$08.00+0     doi:10.1128/JB.187.3.1135-1160.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Genome-Wide Expression Analysis Indicates that FNR of Escherichia coli K-12 Regulates a Large Number of Genes of Unknown Function{dagger}

Yisheng Kang,1 K. Derek Weber,2 Yu Qiu,1 Patricia J. Kiley,2 and Frederick R. Blattner1*

Department of Genetics,1 Department of Biomolecular Chemistry, University of Wisconsin, Madison, Wisconsin2

Received 10 June 2004/ Accepted 11 October 2004

The major regulator controlling the physiological switch between aerobic and anaerobic growth conditions in Escherichia coli is the DNA binding protein FNR. To identify genes controlled by FNR, we used Affymetrix Antisense GeneChips to compare global gene expression profiles from isogenic MG1655 wild-type and {Delta}fnr strains grown in glucose minimal media under aerobic or anaerobic conditions. We found that 297 genes contained within 184 operons were regulated by FNR and/or by O2 levels. The expression of many genes known to be involved in anaerobic respiration and fermentation was increased under anaerobic growth conditions, while that of genes involved in aerobic respiration and the tricarboxylic acid cycle were repressed as expected. The expression of nine operons associated with acid resistance was also increased under anaerobic growth conditions, which may reflect the production of acidic fermentation products. Ninety-one genes with no presently defined function were also altered in expression, including seven of the most highly anaerobically induced genes, six of which we found to be directly regulated by FNR. Classification of the 297 genes into eight groups by k-means clustering analysis indicated that genes with common gene expression patterns also had a strong functional relationship, providing clues for studying the function of unknown genes in each group. Six of the eight groups showed regulation by FNR; while some expression groups represent genes that are simply activated or repressed by FNR, others, such as those encoding functions for chemotaxis and motility, showed a more complex pattern of regulation. A computer search for FNR DNA binding sites within predicted promoter regions identified 63 new sites for 54 genes. We suggest that E. coli MG1655 has a larger metabolic potential under anaerobic conditions than has been previously recognized.


* Corresponding author. Mailing address: Department of Genetics, 425 Henry Mall, University of Wisconsin, Madison, WI 53706. Phone: (608) 890-0191. Fax: (608) 263-7459. E-mail: fred{at}genome.wisc.edu.

{dagger} Supplemental material for this article may be found at http://jb.asm.org/.


Journal of Bacteriology, February 2005, p. 1135-1160, Vol. 187, No. 3
0021-9193/05/$08.00+0     doi:10.1128/JB.187.3.1135-1160.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Eraso, J. M., Kaplan, S. (2009). Regulation of Gene Expression by PrrA in Rhodobacter sphaeroides 2.4.1: Role of Polyamines and DNA Topology. J. Bacteriol. 191: 4341-4352 [Abstract] [Full Text]  
  • Xu, M., Busby, S. J. W., Browning, D. F. (2009). Activation and Repression at the Escherichia coli ynfEFGHI Operon Promoter. J. Bacteriol. 191: 3172-3176 [Abstract] [Full Text]  
  • Wu, Y., Outten, F. W. (2009). IscR Controls Iron-Dependent Biofilm Formation in Escherichia coli by Regulating Type I Fimbria Expression. J. Bacteriol. 191: 1248-1257 [Abstract] [Full Text]  
  • Collado-Vides, J., Salgado, H., Morett, E., Gama-Castro, S., Jimenez-Jacinto, V., Martinez-Flores, I., Medina-Rivera, A., Muniz-Rascado, L., Peralta-Gil, M., Santos-Zavaleta, A. (2009). Bioinformatics Resources for the Study of Gene Regulation in Bacteria. J. Bacteriol. 191: 23-31 [Full Text]  
  • Yan, A., Kiley, P. J. (2008). Dissecting the Role of the N-Terminal Region of the Escherichia coli Global Transcription Factor FNR. J. Bacteriol. 190: 8230-8233 [Abstract] [Full Text]  
  • Eraso, J. M., Roh, J. H., Zeng, X., Callister, S. J., Lipton, M. S., Kaplan, S. (2008). Role of the Global Transcriptional Regulator PrrA in Rhodobacter sphaeroides 2.4.1: Combined Transcriptome and Proteome Analysis. J. Bacteriol. 190: 4831-4848 [Abstract] [Full Text]  
  • Nikel, P. I., de Almeida, A., Pettinari, M. J., Mendez, B. S. (2008). The Legacy of HfrH: Mutations in the Two-Component System CreBC Are Responsible for the Unusual Phenotype of an Escherichia coli arcA Mutant. J. Bacteriol. 190: 3404-3407 [Abstract] [Full Text]  
  • Musken, A., Bielaszewska, M., Greune, L., Schweppe, C. H., Muthing, J., Schmidt, H., Schmidt, M. A., Karch, H., Zhang, W. (2008). Anaerobic Conditions Promote Expression of Sfp Fimbriae and Adherence of Sorbitol-Fermenting Enterohemorrhagic Escherichia coli O157:NM to Human Intestinal Epithelial Cells. Appl. Environ. Microbiol. 74: 1087-1093 [Abstract] [Full Text]  
  • Partridge, J. D., Browning, D. F., Xu, M., Newnham, L. J., Scott, C., Roberts, R. E., Poole, R. K., Green, J. (2008). Characterization of the Escherichia coli K-12 ydhYVWXUT operon: regulation by FNR, NarL and NarP. Microbiology 154: 608-618 [Abstract] [Full Text]  
  • Lin, H.-Y., Bledsoe, P. J., Stewart, V. (2007). Activation of yeaR-yoaG Operon Transcription by the Nitrate-Responsive Regulator NarL Is Independent of Oxygen- Responsive Regulator Fnr in Escherichia coli K-12. J. Bacteriol. 189: 7539-7548 [Abstract] [Full Text]  
  • Boulette, M. L., Payne, S. M. (2007). Anaerobic Regulation of Shigella flexneri Virulence: ArcA Regulates fur and Iron Acquisition Genes. J. Bacteriol. 189: 6957-6967 [Abstract] [Full Text]  
  • Inui, M., Suda, M., Okino, S., Nonaka, H., Puskas, L. G., Vertes, A. A., Yukawa, H. (2007). Transcriptional profiling of Corynebacterium glutamicum metabolism during organic acid production under oxygen deprivation conditions. Microbiology 153: 2491-2504 [Abstract] [Full Text]  
  • Reigstad, C. S., Hultgren, S. J., Gordon, J. I. (2007). Functional Genomic Studies of Uropathogenic Escherichia coli and Host Urothelial Cells when Intracellular Bacterial Communities Are Assembled. J. Biol. Chem. 282: 21259-21267 [Abstract] [Full Text]  
  • Fuchs, S., Pane-Farre, J., Kohler, C., Hecker, M., Engelmann, S. (2007). Anaerobic Gene Expression in Staphylococcus aureus. J. Bacteriol. 189: 4275-4289 [Abstract] [Full Text]  
  • Partridge, J. D., Poole, R. K., Green, J. (2007). The Escherichia coli yhjA gene, encoding a predicted cytochrome c peroxidase, is regulated by FNR and OxyR. Microbiology 153: 1499-1509 [Abstract] [Full Text]  
  • Mettert, E. L., Kiley, P. J. (2007). Contributions of [4Fe-4S]-FNR and Integration Host Factor to fnr Transcriptional Regulation. J. Bacteriol. 189: 3036-3043 [Abstract] [Full Text]  
  • Partridge, J. D., Sanguinetti, G., Dibden, D. P., Roberts, R. E., Poole, R. K., Green, J. (2007). Transition of Escherichia coli from Aerobic to Micro-aerobic Conditions Involves Fast and Slow Reacting Regulatory Components. J. Biol. Chem. 282: 11230-11237 [Abstract] [Full Text]  
  • Jervis, A. J., Green, J. (2007). In Vivo Demonstration of FNR Dimers in Response to Lower O2 Availability. J. Bacteriol. 189: 2930-2932 [Abstract] [Full Text]  
  • Fink, R. C., Evans, M. R., Porwollik, S., Vazquez-Torres, A., Jones-Carson, J., Troxell, B., Libby, S. J., McClelland, M., Hassan, H. M. (2007). FNR Is a Global Regulator of Virulence and Anaerobic Metabolism in Salmonella enterica Serovar Typhimurium (ATCC 14028s). J. Bacteriol. 189: 2262-2273 [Abstract] [Full Text]  
  • Yee, N., Ma, J., Dalia, A., Boonfueng, T., Kobayashi, D. Y. (2007). Se(VI) Reduction and the Precipitation of Se(0) by the Facultative Bacterium Enterobacter cloacae SLD1a-1 Are Regulated by FNR. Appl. Environ. Microbiol. 73: 1914-1920 [Abstract] [Full Text]  
  • Pullan, S. T., Gidley, M. D., Jones, R. A., Barrett, J., Stevanin, T. M., Read, R. C., Green, J., Poole, R. K. (2007). Nitric Oxide in Chemostat-Cultured Escherichia coli Is Sensed by Fnr and Other Global Regulators: Unaltered Methionine Biosynthesis Indicates Lack of S Nitrosation. J. Bacteriol. 189: 1845-1855 [Abstract] [Full Text]  
  • Grainger, D. C., Aiba, H., Hurd, D., Browning, D. F., Busby, S. J. W. (2007). Transcription factor distribution in Escherichia coli: studies with FNR protein. Nucleic Acids Res 35: 269-278 [Abstract] [Full Text]  
  • Partridge, J. D., Scott, C., Tang, Y., Poole, R. K., Green, J. (2006). Escherichia coli Transcriptome Dynamics during the Transition from Anaerobic to Aerobic Conditions. J. Biol. Chem. 281: 27806-27815 [Abstract] [Full Text]  
  • Crack, J. C., Green, J., Le Brun, N. E., Thomson, A. J. (2006). Detection of Sulfide Release from the Oxygen-sensing [4Fe-4S] Cluster of FNR. J. Biol. Chem. 281: 18909-18913 [Abstract] [Full Text]  
  • Oshima, T., Biville, F. (2006). Functional identification of ygiP as a positive regulator of the ttdA-ttdB-ygjE operon. Microbiology 152: 2129-2135 [Abstract] [Full Text]  
  • Patridge, E. V., Ferry, J. G. (2006). WrbA from Escherichia coli and Archaeoglobus fulgidus Is an NAD(P)H:Quinone Oxidoreductase.. J. Bacteriol. 188: 3498-3506 [Abstract] [Full Text]  
  • Constantinidou, C., Hobman, J. L., Griffiths, L., Patel, M. D., Penn, C. W., Cole, J. A., Overton, T. W. (2006). A Reassessment of the FNR Regulon and Transcriptomic Analysis of the Effects of Nitrate, Nitrite, NarXL, and NarQP as Escherichia coli K12 Adapts from Aerobic to Anaerobic Growth. J. Biol. Chem. 281: 4802-4815 [Abstract] [Full Text]  
  • Guedon, E., Sperandio, B., Pons, N., Ehrlich, S. D., Renault, P. (2005). Overall control of nitrogen metabolism in Lactococcus lactis by CodY, and possible models for CodY regulation in Firmicutes. Microbiology 151: 3895-3909 [Abstract] [Full Text]  
  • Dibden, D. P., Green, J. (2005). In vivo cycling of the Escherichia coli transcription factor FNR between active and inactive states. Microbiology 151: 4063-4070 [Abstract] [Full Text]  
  • Stewart, V., Bledsoe, P. J. (2005). Fnr-, NarP- and NarL-Dependent Regulation of Transcription Initiation from the Haemophilus influenzae Rd napF (Periplasmic Nitrate Reductase) Promoter in Escherichia coli K-12. J. Bacteriol. 187: 6928-6935 [Abstract] [Full Text]  
  • Mao, L., Mackenzie, C., Roh, J. H., Eraso, J. M., Kaplan, S., Resat, H. (2005). Combining microarray and genomic data to predict DNA binding motifs. Microbiology 151: 3197-3213 [Abstract] [Full Text]  
  • Plantinga, T. H., van der Does, C., Tomkiewicz, D., van Keulen, G., Konings, W. N., Driessen, A. J. M. (2005). Deletion of the yiaMNO transporter genes affects the growth characteristics of Escherichia coli K-12. Microbiology 151: 1683-1689 [Abstract] [Full Text]