WWOX modulates the ATR-mediated DNA damage checkpoint response

Mohammad Abu-Odeh, Nyla A. Hereema, Rami I. Aqeilan

Research output: Contribution to journalArticlepeer-review

Abstract

For many decades genomic instability is considered one of the hallmarks of cancer. Role of the tumor suppressor WWOX (WW domain-containing oxidoreductase) in DNA damage response upon double strand breaks has been recently revealed. Here we demonstrate unforeseen functions for WWOX upon DNA single strand breaks (SSBs) checkpoint activation. We found that WWOX levels are induced following SSBs and accumulate in the nucleus. WWOX deficiency is associated with reduced activation of ataxia telangiectasia and Rad3-related protein (ATR) checkpoint proteins and increased chromosomal breaks. At the molecular level, we show that upon SSBs WWOX is modified at lysine 274 by ubiquitination mediated by the ubiquitin E3 ligase ITCH and interacts with ataxia telangiectasia-mutated (ATM). Interestingly, ATM inhibition was associated with reduced activation of ATR checkpoint proteins suggesting that WWOX manipulation of ATR checkpoint proteins is ATM-dependent. Taken together, the present findings indicate that WWOX plays a key role in ATR checkpoint activation, while its absence might facilitate genomic instability.

Original languageEnglish
Pages (from-to)4344-4355
Number of pages12
JournalOncotarget
Volume7
Issue number4
DOIs
StatePublished - 2016

Keywords

  • ATR
  • Common fragile sites
  • Genomic instability
  • ITCH
  • WWOX

All Science Journal Classification (ASJC) codes

  • Oncology

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