Genome-Wide Expression Analysis Indicates that FNR ofEscherichia coliK-12 Regulates a Large Number of Genes of Unknown Function
Open Access
- 1 February 2005
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 187 (3) , 1135-1160
- https://doi.org/10.1128/jb.187.3.1135-1160.2005
Abstract
The major regulator controlling the physiological switch between aerobic and anaerobic growth conditions inEscherichia coliis 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 Δfnrstrains 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 O2levels. 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 byk-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 thatE. coliMG1655 has a larger metabolic potential under anaerobic conditions than has been previously recognized.Keywords
This publication has 102 references indexed in Scilit:
- Probing the ArcA-P Modulon of Escherichia coli by Whole Genome Transcriptional Analysis and Sequence Recognition ProfilingJournal of Biological Chemistry, 2004
- Statistical significance for genomewide studiesProceedings of the National Academy of Sciences, 2003
- Nitrate- and nitrite-responsive sensors NarX and NarQ of proteobacteriaBiochemical Society Transactions, 2003
- Computational identification of Cis -regulatory elements associated with groups of functionally related genes in Saccharomyces cerevisiae 1 1Edited by F. E. CohenJournal of Molecular Biology, 2000
- A mutational study of the ArcA-P binding sequences in the aldA promoter of Escherichia coliMolecular Genetics and Genomics, 1999
- The Complete Genome Sequence of Escherichia coli K-12Science, 1997
- Nitrite and nitrate regulation at the promoters of two Escherichia coli operons encoding nitrite reductase: identification of common target heptamers for both NarP‐ and NarL‐dependent regulationMolecular Microbiology, 1994
- Isolation and characterization of hypophosphite‐resistant mutants of Escherichia coli: identification of the FocA protein, encoded by the pfl operon, as a putative formate transporterMolecular Microbiology, 1994
- The nik operon of Escherichia coli encodes a periplasmic binding‐protein‐dependent transport system for nickelMolecular Microbiology, 1993
- Contribution of the fnr and arcA gene products in coordinate regulation of cytochrome o and d oxidase (cyoABCDE and cydAB) genes in Escherichia coliFEMS Microbiology Letters, 1992