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Stabilization of stalled DNA replication forks by the BRCA2 breast cancer susceptibility protein

Research output: Contribution to journalArticle

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Author(s)

Mikhail Lomonosov, Shubha Anand, Mahesh Sangrithi, Rachel Davies, Ashok R Venkitaraman

School/Research organisations

Abstract

How dividing mammalian cells overcome blocks to DNA replication by DNA damage, depleted nucleotide pools, or template-bound proteins is unclear. Here, we show that the response to blocked replication requires BRCA2, a suppressor of human breast cancer. By using two-dimensional gel electrophoresis, we demonstrate that Y-shaped DNA junctions at stalled replication forks disappear during genome-wide replication arrest in BRCA2-deficient cells, accompanied by double-strand DNA breakage. But activation of the replication checkpoint kinase Chk2 is unaffected, defining an unexpected function for BRCA2 in stabilizing DNA structures at stalled forks. We propose that in BRCA2 deficiency and related chromosomal instability diseases, the breakdown of replication forks, which arrest or pause during normal cell growth, triggers spontaneous DNA breakage, leading to mutability and cancer predisposition.

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Original languageEnglish
Pages (from-to)3017-22
Number of pages6
JournalGenes & Development
Volume17
Issue number24
DOIs
Publication statusPublished - 15 Dec 2003

    Research areas

  • Animals, BRCA2 Protein/physiology, Breast Neoplasms/genetics, Cell Cycle/physiology, Cells, Cultured, Checkpoint Kinase 2, DNA/chemistry, DNA Damage, DNA Repair/genetics, DNA Replication, Disease Susceptibility, Electrophoresis, Gel, Two-Dimensional, Enzyme Inhibitors/pharmacology, Female, Fibroblasts/metabolism, Hydroxyurea/pharmacology, Mice, Mice, Knockout, Phosphorylation, Protein-Serine-Threonine Kinases/metabolism, Replication Origin

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