AHNAK interacts with the DNA ligase IV–XRCC4 complex and stimulates DNA ligase IV-mediated double-stranded ligation
pmid: 15177040
AHNAK interacts with the DNA ligase IV–XRCC4 complex and stimulates DNA ligase IV-mediated double-stranded ligation
AHNAK is a high molecular weight protein that is under-expressed in several radiosensitive neuroblastoma cell lines. Using immunoaffinity purification or purified proteins, we show that AHNAK interacts specifically with the DNA ligase IV-XRCC4 complex, a complex that functions in DNA non-homologous end-joining. Furthermore, AHNAK and the DNA ligase IV-XRCC4 complex co-immunoprecipitate demonstrating an in vivo interaction. This interaction is specific and is not observed with other DNA ligases nor with other components of the DNA non-homologous end-joining machinery. We characterised AHNAK as a protein that stimulates the double-stranded (DS) ligation activity of DNA ligase IV-XRCC4. We show that AHNAK has weak DNA-binding activity and forms a stable complex with the DNA ligase IV-XRCC4 complex on DNA. AHNAK is also able to link two DNA molecules to a similar extent to that previously reported for Ku. Together, these findings demonstrate new activities for AHNAK, and raise the possibility that it may function to modulate DNA non-homologous end-joining.
- University of California, San Francisco United States
- University of Sussex United Kingdom
- Cancer Research Institute United States
DNA Ligases, DNA Repair, Blotting, Western, Membrane Proteins, Electrophoretic Mobility Shift Assay, Chromatography, Ion Exchange, Precipitin Tests, Neoplasm Proteins, DNA-Binding Proteins, DNA Ligase ATP, Organophosphorus Compounds, Sequence Analysis, Protein, Chromatography, Gel, Humans
DNA Ligases, DNA Repair, Blotting, Western, Membrane Proteins, Electrophoretic Mobility Shift Assay, Chromatography, Ion Exchange, Precipitin Tests, Neoplasm Proteins, DNA-Binding Proteins, DNA Ligase ATP, Organophosphorus Compounds, Sequence Analysis, Protein, Chromatography, Gel, Humans
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