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Mechanism of mitotic recombination: insights from C. elegans.
Belan, Ondrej; Anand, Roopesh; Boulton, Simon J.
Affiliation
  • Belan O; DSB Repair Metabolism Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Anand R; DSB Repair Metabolism Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Boulton SJ; DSB Repair Metabolism Laboratory, The Francis Crick Institute, London NW1 1AT, UK. Electronic address: simon.boulton@crick.ac.uk.
Curr Opin Genet Dev ; 71: 10-18, 2021 12.
Article in En | MEDLINE | ID: mdl-34186335
ABSTRACT
Homologous recombination (HR) plays a critical role in largely error-free repair of mitotic and meiotic DNA double-strand breaks (DSBs). DSBs are one of the most deleterious DNA lesions, which are repaired by non-homologous end joining (NHEJ), homologous recombination (HR) or, if compromised, micro-homology mediated end joining (MMEJ). If left unrepaired, DSBs can lead to cell death or if repaired incorrectly can result in chromosome rearrangements that drive cancer development. Here, we describe recent advances in the field of mitotic HR made using Caenorhabditis elegans roundworm, as a model system.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caenorhabditis elegans / DNA End-Joining Repair Limits: Animals Language: En Journal: Curr Opin Genet Dev Journal subject: GENETICA Year: 2021 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caenorhabditis elegans / DNA End-Joining Repair Limits: Animals Language: En Journal: Curr Opin Genet Dev Journal subject: GENETICA Year: 2021 Document type: Article Affiliation country: United kingdom