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PMID: 14726021 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Repair of DNA double strand breaks by non-homologous end joining.

Biochimie ·Vol. 85 ·No. 11 ·2003-11-00 ·Pages 1161-73

Lees-Miller SP, Meek K

Abstract

DNA double strand breaks (DSB) are the most serious form of DNA damage. If not repaired they can lead to cell death. If misrepaired DSBs contribute to chromosomal aberrations and genomic instability. Non-homologous end joining (NHEJ) is one of two major pathways for the repair of DSBs in human cells. Proteins known to be required for NHEJ include the DNA-dependent protein kinase (DNA-PK), XRCC4, DNA ligase IV, and Artemis. This review discusses how these and other accessory proteins may function in the repair of DSBs produced by ionizing radiation (IR) and by V(D)J recombination.

MeSH Terms
Animals DNA Damage DNA Repair DNA-Activated Protein Kinase DNA-Binding Proteins/genetics,physiology Evolution, Molecular Humans Nuclear Proteins Protein Serine-Threonine Kinases/genetics,physiology,therapeutic use Recombination, Genetic/genetics,physiology
Chemicals
DNA-Binding Proteins Nuclear Proteins DNA-Activated Protein Kinase PRKDC protein, human Protein Serine-Threonine Kinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lees-Miller S P
Cancer Biology Research Group, Department of Biochemistry and Molecular Biology, University of Calgary, 3330 Hospital Drive, NW, Calgary, Alta., Canada T2N 4N1. leesmill@ucalgary.ca
Meek K
Article Info
Journal
Biochimie
Abbr.
Biochimie
ISSN
0300-9084
Published
2003-11-00
Pages
1161-73
Language
English
Region
France
NLM ID
1264604
Subset
IM
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