Possible role of WRN protein in cellular response induced by a little DNA damage

Junya Kobayashi, Michiyo Okui, Kenshi Komatsu, David J. Chen

Research output: Contribution to journalArticle

Abstract

Werner syndrome (WS) is an autosomal recessive disorder associated with premature aging and cancer predisposition caused by mutations at the WRN gene. Several recent reports suggest that accumulation of DNA damage could lead to premature cellular aging. Therefore, WRN might function in DNA damage response, particularly DNA repair. Here, we investigated the role of WRN in DNA repair and genome integrity. WRN protein rapidly accumulated at DNA damage sites and formed discrete nuclear foci only during S phase, but not in Gl phase. WRN-defective WS cells showed the spontaneous accumulation of y-H2AX (DSB marker), suggesting that WRN could function to repair the S phase-dependent DNA damage. However, WS cells showed homologous recombination (HR) at normal level, although HR repair functions preferentially during the S phase. Translesion DNA synthesis (TLS) is known as another repair pathway for S phase-dependent DNA damage. WS cells exhibit an increase in spontaneous focus formation of polí and Rad18, which are important for TLS regulation. WS cells also showed the spontaneous ubiquitination of PCNA and increased poln-related gene mutation. Taken together, WRN could work for the regulation of TLS pathway and might also be important to maintain genome integrity under a little DNA damage by tritium.

Original languageEnglish (US)
Pages (from-to)1186-1189
Number of pages4
JournalFusion Science and Technology
Volume60
Issue number3
DOIs
StatePublished - Oct 2011

ASJC Scopus subject areas

  • Civil and Structural Engineering
  • Nuclear and High Energy Physics
  • Nuclear Energy and Engineering
  • Materials Science(all)
  • Mechanical Engineering

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