Journal
CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 66, Issue 6, Pages 1039-1056Publisher
SPRINGER BASEL AG
DOI: 10.1007/s00018-009-8740-3
Keywords
DNA repair; genome stability; checkpoint; nonhomologous end joining; homologous recombination; repair pathway choice
Categories
Funding
- Spanish Ministry of Science and Education [BFU2008 - 05260, CDS2007-0015]
- Junta de Andalucia [CVI102, CVI624]
- Spanish Ministry of Science and Education
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DNA double-strand breaks (DSBs) arise in cells from endogenous and exogenous attacks on the DNA backbone, but also as a direct consequence of replication failures. Proper repair of all these DSBs is essential for genome stability. Repair of broken chromosomes is a challenge for dividing cells that need to distribute equal genetic information to daughter cells. Consequently, eukaryotic organisms have evolved multi-potent and efficient mechanisms to repair DSBs that are primarily divided into two types of pathways: nonhomologous end joining (NHEJ) and homologous recombination (HR). Here we briefly describe how eukaryotic cells sense DSBs and trigger cell cycle arrest to allow repair, and we review the mechanisms of both NHEJ and HR pathways and the choice between them. (Part of a Multi-author Review).
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