Ataxia telangiectasia-related protein is involved in the phosphorylation of BRCA1 following deoxyribonucleic acid damage.
The breast/ovarian cancer susceptibility gene BRCA1 exerts its tumor suppressor function, at least in part, by participating in DNA repair and/or DNA damage-responsive pathways. BRCA1 protein is hyperphosphorylated following various DNA-damaging events. Here, we report that the ataxia telangiectasia mutated protein-related protein kinase (ATR) is involved in the phosphorylation of ... BRCA1 following gamma radiation and hydroxyurea treatment. We have shown that ATR can phosphorylate several BRCA1 fragments in vitro and that a kinase-inactive mutant of ATR interacts with BRCA1 in vivo. Taken together, these results suggest that ATR directly phosphorylates BRCA1 following DNA damage.
Mesh Terms:
1-Phosphatidylinositol 3-Kinase, Androstadienes, Antineoplastic Agents, BRCA1 Protein, Breast Neoplasms, Cell Cycle Proteins, DNA Damage, DNA, Neoplasm, DNA-Binding Proteins, Enzyme Inhibitors, Humans, Hydroxyurea, Phosphorylation, Protein-Serine-Threonine Kinases, Tumor Cells, Cultured, Tumor Suppressor Proteins
1-Phosphatidylinositol 3-Kinase, Androstadienes, Antineoplastic Agents, BRCA1 Protein, Breast Neoplasms, Cell Cycle Proteins, DNA Damage, DNA, Neoplasm, DNA-Binding Proteins, Enzyme Inhibitors, Humans, Hydroxyurea, Phosphorylation, Protein-Serine-Threonine Kinases, Tumor Cells, Cultured, Tumor Suppressor Proteins
Cancer Res.
Date: Sep. 15, 2000
PubMed ID: 11016625
View in: Pubmed Google Scholar
Download Curated Data For This Publication
74150
Switch View:
- Interactions 3