Issue 12, 2009

Systems-level approaches for identifying and analyzing genetic interaction networks in Escherichia coli and extensions to other prokaryotes

Abstract

Molecular interactions define the functional organization of the cell. Epistatic (genetic, or genegene) interactions, one of the most informative and commonly encountered forms of functional relationships, are increasingly being used to map process architecture in model eukaryotic organisms. In particular, ‘systems-level’ screens in yeast and worm aimed at elucidating genetic interaction networks have led to the generation of models describing the global modular organization of gene products and protein complexes within a cell. However, comparable data for prokaryotic organisms have not been available. Given its ease of growth and genetic manipulation, the Gram-negative bacterium Escherichia coli appears to be an ideal model system for performing comprehensive genome-scale examinations of genetic redundancy in bacteria. In this review, we highlight emerging experimental and computational techniques that have been developed recently to examine functional relationships and redundancy in E. coli at a systems-level, and their potential application to prokaryotes in general. Additionally, we have scanned PubMed abstracts and full-text published articles to manually curate a list of ∼200 previously reported synthetic sick or lethal genetic interactions in E. coli derived from small-scale experimental studies.

Graphical abstract: Systems-level approaches for identifying and analyzing genetic interaction networks in Escherichia coli and extensions to other prokaryotes

Supplementary files

Article information

Article type
Review Article
Submitted
14 Apr 2009
Accepted
24 Jun 2009
First published
31 Jul 2009

Mol. BioSyst., 2009,5, 1439-1455

Systems-level approaches for identifying and analyzing genetic interaction networks in Escherichia coli and extensions to other prokaryotes

M. Babu, G. Musso, J. J. Díaz-Mejía, G. Butland, J. F. Greenblatt and A. Emili, Mol. BioSyst., 2009, 5, 1439 DOI: 10.1039/B907407D

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