Abstract
Annual Review of Microbiology
Vol. 59:
357-377
(Volume publication date October 2005)
(doi:10.1146/annurev.micro.59.031805.133658)
First published online as a Review in Advance on June 14, 2005GENOME-WIDE RESPONSES TO DNA-DAMAGING AGENTS Rebecca C. Fry1, Thomas J. Begley2, and Leona D. Samson1 1Biological Engineering Division and Center for Environmental Health Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139; email: rfry@mit.edu, lsamson@mit.edu 2Department of Biomedical Sciences and Gen*NY*Sis Center for Excellence in Cancer Genomics, University at Albany-SUNY, Rensselaer, New York 12144; email: tbegley@albany.edu Abstract Genome-wide studies of mRNA regulation and phenotypic responses have shown that eukaryotic cells mount a robust and multifaceted response upon exposure to DNA-damaging agents. The integration of theses studies over frameworks provided by protein-protein interactions, protein-DNA interactions, and subcellular localization information have led to the identification of networked responses to damage. Taken together, these studies illustrate that cellular protection from DNA and other macromolecular damage involves an intricate network of proteins involved in many different cellular functions, some of them expected (e.g., DNA repair and cell cycle checkpoints) but many of them unexpected (e.g., protein trafficking and degradation). This review highlights many of the studies that detail genome-wide responses to DNA-damaging agents and examines how these datasets have been used to build a systems view of cellular responses to damage. Terms and Definitions DNA-damaging agents: toxicants that alter DNA and may also cause damage to other macromolecular species Networks: interactions between macromolecules including proteins or DNA Systems biology: the integration of information regarding all types of biological information (DNA, RNA, protein, protein interactions, cells, tissues, etc.) to understand the workings of a biological system Acronyms 4NQO: 4-nitroquinoline N-oxide AP: apurinic/apyrimidinic BCNU: 1,3-bis(2-chloroethyl)-1-nitrosourea BER: base excision repair din: damage-inducible DDR: DNA-damage response ER: endoplasmic reticulum ESR: environmental stress response GFP: green fluorescent protein MNNG: N-methyl-N′-nitro-N-nitrosoguanidine MMR: mismatch repair MMS: methyl methanesulfonate NER: nucleotide excision repair RNR: ribonucleotide reductase SGA: synthetic genetic array SOM: self-organizing map t-BuOOH: tert-butyl hydroperoxide UV: ultra violet The Chemical Genomic Portrait of Yeast: Uncovering a Phenotype for All Genes M. E. Hillenmeyer, E. Fung, J. Wildenhain, S. E. Pierce, S. Hoon, W. Lee, M. Proctor, R. P. St.Onge, M. Tyers, D. Koller, R. B. Altman, R. W. Davis, C. Nislow, G. Giaever Science 320(5874):362-365 (2008) A systems approach to delineate functions of paralogous transcription factors: Role of the Yap family in the DNA damage response Proceedings of the National Academy of Sciences 105(8):2934-2939 (2008) Immunomodulation by fluoroquinolones and other antibacterial agents European Journal of Clinical Investigation 36(10):671-673 (2006)
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