Abstract:
:The hereditary breast and ovarian cancer predisposition genes, BRCA1 and BRCA2, participate in the repair of DNA double strand breaks by homologous recombination. Circumstantial evidence implicates these genes in recombinational responses to DNA polymerase stalling during the S phase of the cell cycle. These responses play a key role in preventing genomic instability and cancer. Here, we review the current literature implicating the BRCA pathway in HR at stalled replication forks and explore the hypothesis that BRCA1 and BRCA2 participate in the recombinational resolution of single stranded DNA lesions termed "daughter strand gaps", generated during replication across a damaged DNA template.
journal_name
DNA Repair (Amst)journal_title
DNA repairauthors
Nagaraju G,Scully Rdoi
10.1016/j.dnarep.2007.02.020subject
Has Abstractpub_date
2007-07-01 00:00:00pages
1018-31issue
7eissn
1568-7864issn
1568-7856pii
S1568-7864(07)00071-7journal_volume
6pub_type
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