A novel role for hSMG-1 in stress granule formation

  • James A. L. Brown
  • , Tara L. Roberts
  • , Renee Richards
  • , Rick Woods
  • , Geoff Birrell
  • , Y. C. Lim
  • , Shigeo Ohno
  • , Akio Yamashita
  • , Robert T. Abraham
  • , Nuri Gueven
  • , Martin F. Lavin

Research output: Contribution to journalArticlepeer-review

40 Citations (Scopus)

Abstract

hSMG-1 is a member of the phosphoinositide 3 kinase-like kinase (PIKK) family with established roles in nonsense-mediated decay (NMD) of mRNA containing premature termination codons and in genotoxic stress responses to DNA damage. We report here a novel role for hSMG-1 in cytoplasmic stress granule (SG) formation. Exposure of cells to stress causing agents led to the localization of hSMG-1 to SG, identified by colocalization with TIA-1, G3BP1, and eIF4G. hSMG-1 small interfering RNA and the PIKK inhibitor wortmannin prevented formation of a subset of SG, while specific inhibitors of ATM, DNA-PK cs, or mTOR had no effect. Exposure of cells to H 2O 2 and sodium arsenite induced (S/T)Q phosphorylation of proteins. While Upf2 and Upf1, an essential substrate for hSMG-1 in NMD, were present in SG, NMD-specific Upf1 phosphorylation was not detected in SG, indicating hSMG-1's role in SG is separate from classical NMD. Thus, SG formation appears more complex than originally envisaged and hSMG-1 plays a central role in this process.
Original languageEnglish
Pages (from-to)4417-4429
Number of pages13
JournalMolecular and Cellular Biology
Volume31
Issue number22
DOIs
Publication statusPublished - 2011

Keywords

  • DNA
  • cytoplasmic granules
  • genetic toxicology
  • phosphoinositides

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