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A novel role for hsmg-1 in stress granule formation

  • James Andrew Lawrence Brown
  • , T. L. Roberts
  • , R. Richards
  • , R. Woods
  • , G. Birrell
  • , Y. C. Lim
  • , S. Ohno
  • , A. Yamashita
  • , R. T. Abraham
  • , N. Gueven
  • , M. F. Lavin

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-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(2)O(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 (Ireland)
JournalMolecular and Cellular Biology
DOIs
Publication statusPublished - 12 Sept 2011

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