hSSB1 interacts directly with the MRN complex stimulating its recruitment to DNA double-strand breaks and its endo-nuclease activity |
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Authors: | Richard Derek J Cubeddu Liza Urquhart Aaron J Bain Amanda Bolderson Emma Menon Dinoop White Malcolm F Khanna Kum Kum |
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Affiliation: | 1Signal Transduction Laboratory, Queensland Institute of Medical Research, Brisbane, Queensland 4006, 2School of Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW 2006, Australia and 3Biomedical Sciences Research Complex, University of St. Andrews, North Haugh, St Andrews, Fife KY16 9ST, UK |
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Abstract: | hSSB1 is a recently discovered single-stranded DNA binding protein that is essential for efficient repair of DNA double-strand breaks (DSBs) by the homologous recombination pathway. hSSB1 is required for the efficient recruitment of the MRN complex to sites of DSBs and for the efficient initiation of ATM dependent signalling. Here we explore the interplay between hSSB1 and MRN. We demonstrate that hSSB1 binds directly to NBS1, a component of the MRN complex, in a DNA damage independent manner. Consistent with the direct interaction, we observe that hSSB1 greatly stimulates the endo-nuclease activity of the MRN complex, a process that requires the C-terminal tail of hSSB1. Interestingly, analysis of two point mutations in NBS1, associated with Nijmegen breakage syndrome, revealed weaker binding to hSSB1, suggesting a possible disease mechanism. |
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