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PMID: 16153173 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Genome-wide responses to DNA-damaging agents.

Annual review of microbiology ·Vol. 59 ·2005-00-00 ·Pages 357-77

Fry RC, Begley TJ, Samson LD

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.

MeSH Terms
DNA Damage DNA Repair Escherichia coli/genetics Eukaryotic Cells Gene Expression Regulation Genome Genome, Bacterial Genome, Fungal SOS Response, Genetics Saccharomyces cerevisiae/genetics
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Fry Rebecca C
Biological Engineering Division and Center for Environmental Health Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA. [email protected]
Begley Thomas J
Samson Leona D
Article Info
Journal
Annual review of microbiology
Abbr.
Annu Rev Microbiol
ISSN
0066-4227
Published
2005-00-00
Pages
357-77
Language
English
Region
United States
NLM ID
0372370
Subset
IM
Grants
NIEHS NIH HHS · 1K22ES01225101 · United States
NCI NIH HHS · CA55042 · United States
NIEHS NIH HHS · P30 ES002109 · United States
NIEHS NIH HHS · U19-ES11399 · United States
NIEHS NIH HHS · P30-ES002109 · United States
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