Accumulation of Werner protein at DNA double-strand breaks in human cells

Li Lan, Satoshi Nakajima, Kenshi Komatsu, Andre Nussenzweig, Akira Shimamoto, Junko Oshima, Akira Yasui

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    107 Citations (Scopus)

    Abstract

    Werner syndrome is an autosomal recessive accelerated-aging disorder caused by a defect in the WRN gene, which encodes a member of the RecQ family of DNA helicases with an exonuclease activity. In vitro experiments have suggested that WRN functions in several DNA repair processes, but the actual functions of WRN in living cells remain unknown. Here, we analyzed the kinetics of the intranuclear mobilization of WRN protein in response to a variety of types of DNA damage produced locally in the nucleus of human cells. A striking accumulation of WRN was observed at laser-induced double-strand breaks, but not at single-strand breaks or oxidative base damage. The accumulation of WRN at double-strand breaks was rapid, persisted for many hours, and occurred in the absence of several known interacting proteins including polymerase β, poly(ADP-ribose) polymerase 1 (PARP1), Ku80, DNA-dependent protein kinase (DNA-PKcs), NBS1 and histone H2AX. Abolition of helicase activity or deletion of the exonuclease domain had no effect on accumulation, whereas the presence of the HRDC (helicase and RNaseD C-terminal) domain was necessary and sufficient for the accumulation. Our data suggest that WRN functions mainly at DNA double-strand breaks and structures resembling double-strand breaks in living cells, and that an autonomous accumulation through the HRDC domain is the initial response of WRN to the double-strand breaks.

    Original languageEnglish
    Pages (from-to)4153-4162
    Number of pages10
    JournalJournal of cell science
    Volume118
    Issue number18
    DOIs
    Publication statusPublished - 2005 Sep 15

    Keywords

    • Damage accumulation
    • Double-strand breaks
    • HRDC domain
    • Laser irradiation
    • Werner protein

    ASJC Scopus subject areas

    • Cell Biology

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