ATF4 is necessary and sufficient for ER stress-induced upregulation of REDD1 expression

Biochem Biophys Res Commun. 2009 Feb 6;379(2):451-5. doi: 10.1016/j.bbrc.2008.12.079. Epub 2008 Dec 27.


In response to a variety of cell stresses, e.g. endoplasmic reticulum (ER) stress, expression of REDD1 (regulated in development and DNA damage responses) is transcriptionally upregulated. However, the mechanism through which ER stress acts to upregulate REDD1 expression is unknown. In the present study, REDD1 expression was found to be upregulated by ER stress in several cell lines. However, in MEF cells lacking the eIF2alpha kinase PERK, ER stress failed to upregulate REDD1 expression, demonstrating that phosphorylation of eIF2alpha was necessary for the effect. Moreover, ER stress led to upregulated expression of the transcription factor ATF4, but in MEF cells lacking ATF4, REDD1 mRNA expression was not increased by ER stress. In contrast, exogenous expression of ATF4 was sufficient to induce REDD1 expression. Overall, the results suggest that REDD1 expression is upregulated during ER stress through a mechanism involving activation of PERK, phosphorylation of eIF2alpha, and increased ATF4 expression.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Activating Transcription Factor 4 / genetics
  • Activating Transcription Factor 4 / metabolism*
  • Cell Line
  • Endoplasmic Reticulum / metabolism*
  • Eukaryotic Initiation Factor-2 / genetics
  • Eukaryotic Initiation Factor-2 / metabolism
  • Humans
  • Stress, Physiological*
  • Transcription Factors / biosynthesis*
  • Up-Regulation
  • eIF-2 Kinase / metabolism


  • ATF4 protein, human
  • DDIT4 protein, human
  • Eukaryotic Initiation Factor-2
  • Transcription Factors
  • Activating Transcription Factor 4
  • PERK kinase
  • eIF-2 Kinase