Escherichia coli has for decades been the most extensively studied bacterium, making it a key model for the living cell and arguably the one about which the most is known. Yet through genome sequencing we have recently become aware of the true level of level of our ignorance. At least half of the genes discovered are simply of unknown function. In this application we propose to systematically characterize these genes by the use of a set of about 5000 PCR amplified DNA fragments- corresponding to each gene. This PCR geneset will be used to carry out global gene expression experiments at the single gene level. That is, for each gene we will determine how its expression is regulated in response to nutritional, physical and genetic stimuli. This is significant because the regulatory circuitry of E. coli is functionally organized. How a gene is regulated gives information about its function. In addition the PCR geneset will be cloned into vectors designed to facilitate additional analyses including mutational, gene inactivation, gene expression and two hybrid system approaches for determining function. Some of these characterizations will be performed as part of this project. For other approaches the PCR clonesets will be made available to interested investigators. Previous work funded under this grant revealed the power of the global gene expression to discover and identify genes in E. coli, even though the technology available at the time permitted resolution only at the 10 gene level. At the single gene level, a decisive advance in understanding of the organism will be possible.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM035682-13
Application #
2022069
Study Section
Genome Study Section (GNM)
Project Start
1985-04-01
Project End
1999-01-31
Budget Start
1997-02-01
Budget End
1998-01-31
Support Year
13
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Other Health Professions
Type
Schools of Earth Sciences/Natur
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Durfee, Tim; Hansen, Anne-Marie; Zhi, Huijun et al. (2008) Transcription profiling of the stringent response in Escherichia coli. J Bacteriol 190:1084-96
Sharma, Shamik S; Campbell, John W; Frisch, David et al. (2007) Expression of two recombinant chloramphenicol acetyltransferase variants in highly reduced genome Escherichia coli strains. Biotechnol Bioeng 98:1056-70
Sharma, Shamik S; Blattner, Frederick R; Harcum, Sarah W (2007) Recombinant protein production in an Escherichia coli reduced genome strain. Metab Eng 9:133-41
Posfai, Gyorgy; Plunkett 3rd, Guy; Feher, Tamas et al. (2006) Emergent properties of reduced-genome Escherichia coli. Science 312:1044-6
Kang, Yisheng; Weber, K Derek; Qiu, Yu et al. (2005) Genome-wide expression analysis indicates that FNR of Escherichia coli K-12 regulates a large number of genes of unknown function. J Bacteriol 187:1135-60
Hansen, Anne-Marie; Qiu, Yu; Yeh, Norman et al. (2005) SspA is required for acid resistance in stationary phase by downregulation of H-NS in Escherichia coli. Mol Microbiol 56:719-34
Liu, Mingzhu; Durfee, Tim; Cabrera, Julio E et al. (2005) Global transcriptional programs reveal a carbon source foraging strategy by Escherichia coli. J Biol Chem 280:15921-7
Herring, Christopher D; Blattner, Frederick R (2004) Conditional lethal amber mutations in essential Escherichia coli genes. J Bacteriol 186:2673-81
Herring, Christopher D; Blattner, Frederick R (2004) Global transcriptional effects of a suppressor tRNA and the inactivation of the regulator frmR. J Bacteriol 186:6714-20
Kang, Yisheng; Durfee, Tim; Glasner, Jeremy D et al. (2004) Systematic mutagenesis of the Escherichia coli genome. J Bacteriol 186:4921-30

Showing the most recent 10 out of 27 publications