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Break-induced replication: functions and molecular mechanism
Journal article   Peer reviewed

Break-induced replication: functions and molecular mechanism

Anna Malkova and Grzegorz Ira
Current opinion in genetics & development, Vol.23(3), pp.271-279
06/2013
DOI: 10.1016/j.gde.2013.05.007
PMCID: PMC3915057
PMID: 23790415
url
https://scholarworks.indianapolis.iu.edu/bitstreams/d4fbbf0d-4c1f-4cc7-9c68-6d37c7bc3fae/downloadView
Open Access

Abstract

Break-induced replication (BIR) is the pathway of homologous recombination (HR) conserved from phages to eukaryotes that serves to repair DNA breaks that have only one end. BIR contributes to the repair of broken replication forks and allows telomere lengthening in the absence of telomerase. Nonallelic BIR may lead to translocations and other chromosomal rearrangements. In addition, BIR initiated at sites of microhomology can generate copy number variations (CNVs) and complex chromosomal changes. The level of mutagenesis associated with DNA synthesis in BIR is significantly higher than during normal replication. These features make BIR a likely pathway to promote bursts of genetic changes that fuel cancer progression and evolution.
DNA Breaks, Single-Stranded Neoplasms - etiology Neoplasms - genetics Humans Chromosome Aberrations DNA Replication - genetics Homologous Recombination - genetics DNA Copy Number Variations - genetics DNA Repair - genetics Telomere Homeostasis - genetics Genome, Human Neoplasms - pathology

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