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PMID: 8526889 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Menage à trois: double strand break repair, V(D)J recombination and DNA-PK.

Jeggo PA, Taccioli GE, Jackson SP

Abstract

All organisms possess mechanisms to repair double strand breaks (dsbs) generated in their DNA by damaging agents. Site-specific dsbs are also introduced during V(D)J recombination. Four complementation groups of radiosensitive rodent mutants are defective in the repair of dsbs, and are unable to carry out V(D)J recombination effectively. The immune defect in Severe Combined Immunodeficient (scid) mice also results from an inability to undergo effective V(D)J recombination, and scid cell lines display a repair defect and belong to one of these complementation groups. These findings indicate a mechanistic overlap between the processes of DNA repair and V(D)J recombination. Recently, two of the genes defined by these complementation groups have been identified and shown to encode components of DNA-dependent protein kinase (DNA-PK). We review here the three fields which have become linked by these findings, and discuss the involvement of DNA-PK in dsb rejoining and in V(D)J recombination.

MeSH Terms
Animals Biological Evolution DNA Damage DNA Repair DNA-Activated Protein Kinase DNA-Binding Proteins Immunoglobulin Variable Region/genetics Mice Mice, SCID Models, Biological Protein Serine-Threonine Kinases/metabolism Recombination, Genetic
Chemicals
DNA-Binding Proteins Immunoglobulin Variable Region DNA-Activated Protein Kinase Protein Serine-Threonine Kinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Jeggo P A
MRC Cell Mutation Unit, University of Sussex, Brighton, UK.
Taccioli G E
Jackson S P
Article Info
Journal
BioEssays : news and reviews in molecular, cellular and developmental biology
Abbr.
Bioessays
ISSN
0265-9247
Published
1995-11-00
Pages
949-57
Language
English
Region
United States
NLM ID
8510851
Subset
IM
Grants
NIAID NIH HHS · AI-20047 · United States
NIAID NIH HHS · AI-35714 · United States
Wellcome Trust · United Kingdom
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