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PMID: 15380098 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

The mechanism of non-homologous end-joining: a synopsis of synapsis.

DNA repair ·Vol. 3 ·No. 11 ·2004-11-02 ·Pages 1425-35

Weterings E, van Gent DC

Abstract

Repair of DNA double-strand breaks (DSBs) by non-homologous end-joining (NHEJ) is required for resistance to genotoxic agents, such as ionizing radiation, but also for proper development of the vertebrate immune system. Much progress has been made in identifying the factors that are involved in this repair pathway. We are now entering the phase in which we begin to understand basic concepts of the reaction mechanism and regulation of non-homologous end-joining. This review concentrates on novel insights into damage recognition and subsequent tethering, processing and joining of DNA ends.

MeSH Terms
Animals DNA/chemistry,genetics,metabolism DNA Damage DNA Ligase ATP DNA Ligases/metabolism DNA Repair/genetics,immunology,physiology DNA Repair Enzymes/metabolism DNA-Activated Protein Kinase DNA-Binding Proteins/metabolism Genes, Immunoglobulin Genes, T-Cell Receptor Humans Models, Biological Nuclear Proteins Protein Serine-Threonine Kinases/metabolism
Chemicals
DNA-Binding Proteins Nuclear Proteins XRCC4 protein, human DNA DNA-Activated Protein Kinase PRKDC protein, human Protein Serine-Threonine Kinases DNA Ligases DNA Repair Enzymes DNA Ligase ATP
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Weterings Eric
Department of Cell Biology and Genetics, Erasmus Medical Center, P.O. Box 1738, 3000 DR Rotterdam, The Netherlands.
van Gent Dik C
Article Info
Journal
DNA repair
Abbr.
DNA Repair (Amst)
ISSN
1568-7864
Published
2004-11-02
Pages
1425-35
Language
English
Region
Netherlands
NLM ID
101139138
Subset
IM
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