Nature (London), 2008-12, Vol.456 (7223), p.819-823
2008
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Details
- Autor(en) / Beteiligte
- Titel
- DNA double-strand breaks activate a multi-functional genetic program in developing lymphocytes
- Ist Teil von
- Nature (London), 2008-12, Vol.456 (7223), p.819-823
- Ort / Verlag
- London: Nature Publishing Group UK
- Erscheinungsjahr
- 2008
- Quelle
- Psychology & Behavioral Sciences Collection
- Beschreibungen/Notizen
- DNA double-strand breaks are generated by genotoxic agents and by cellular endonucleases as intermediates of several important physiological processes. The cellular response to genotoxic DNA breaks includes the activation of transcriptional programs known primarily to regulate cell-cycle checkpoints and cell survival. DNA double-strand breaks are generated in all developing lymphocytes during the assembly of antigen receptor genes, a process that is essential for normal lymphocyte development. Here we show that in murine lymphocytes these physiological DNA breaks activate a broad transcriptional program. This program transcends the canonical DNA double-strand break response and includes many genes that regulate diverse cellular processes important for lymphocyte development. Moreover, the expression of several of these genes is regulated similarly in response to genotoxic DNA damage. Thus, physiological DNA double-strand breaks provide cues that can regulate cell-type-specific processes not directly involved in maintaining the integrity of the genome, and genotoxic DNA breaks could disrupt normal cellular functions by corrupting these processes.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0028-0836eISSN: 1476-4687DOI: 10.1038/nature07392Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2605662
- Format
- –
- Schlagworte
- Animals, Apoptosis, Ataxia Telangiectasia Mutated Proteins, B-Lymphocytes - drug effects, B-Lymphocytes - metabolism, Biological and medical sciences, Bone marrow, Cell cycle, Cell Cycle Proteins - drug effects, Cell Line, Deoxyribonucleic acid, DNA, DNA Breaks, Double-Stranded, DNA damage, DNA-Binding Proteins - drug effects, Enzyme Inhibitors - pharmacology, Fundamental and applied biological sciences. Psychology, Fundamental immunology, Gene expression, Gene Expression Profiling, Gene Expression Regulation, Developmental - drug effects, Gene Expression Regulation, Developmental - genetics, Genetic aspects, Genetics, Homeodomain Proteins - metabolism, Humanities and Social Sciences, Immunobiology, Kinases, letter, Lymphocytes, Lymphoid cells: ontogeny, maturation, markers, receptors, circulation and recirculation, Mice, Mice, Knockout, Mice, SCID, multidisciplinary, NF-kappa B - metabolism, Physiological aspects, Physiology, Protein-Serine-Threonine Kinases - drug effects, Proteins, Science, Science (multidisciplinary), Tumor Suppressor Proteins - drug effects