Glutamine deprivation induces the expression of GADD45 and GADD153 primarily by mRNA stabilization

J Biol Chem. 1999 Oct 1;274(40):28645-51. doi: 10.1074/jbc.274.40.28645.

Abstract

The expression of the growth arrest- and DNA damage-inducible genes, GADD45 and GADD153/CHOP (C/EBP-homologous protein), as well as GRP78 (glucose-regulated protein of 78 kDa) was examined in several human breast cell lines subjected to acute glutamine (GLN) deprivation. GLN deprivation caused rapid elevation of GADD45 and GADD153/CHOP mRNA levels in cells that were highly dependent upon GLN for growth and viability. Both GADD mRNAs were rapidly elevated up to several hundred-fold. In contrast, GRP78 expression was elevated by no more than 4-fold by GLN deprivation. The magnitude of GADD up-regulation roughly correlated with the extent of GLN dependence of each cell line. The levels of all three mRNAs were responsive to alterations of ambient GLN content in a physiologically relevant concentration range that corresponded to the affinities of cellular GLN transporters. Provision of GLN-derived metabolites partially inhibited the induction of GADD expression in GLN-deprived cells. Nuclear run-on assays and mRNA decay studies suggested that the primary mechanism leading to increased GADD mRNA levels was not transcriptional, but rather that GADD45 and GADD153/CHOP expression were up-regulated in response to GLN deprivation via marked stabilization of these mRNAs. These results suggest that the expression of GADD genes contributes to growth arrest and/or protection from metabolic damage during GLN-poor conditions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • CCAAT-Enhancer-Binding Proteins*
  • Carrier Proteins / genetics
  • Cell Division
  • Cell Line
  • DNA-Binding Proteins / genetics*
  • Endoplasmic Reticulum Chaperone BiP
  • GADD45 Proteins
  • Glutamine / deficiency*
  • Heat-Shock Proteins*
  • Humans
  • Hydrolysis
  • Intracellular Signaling Peptides and Proteins
  • Molecular Chaperones / genetics
  • Proteins / genetics*
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Transcription Factor CHOP
  • Transcription Factors / genetics*
  • Transcription, Genetic
  • Tumor Cells, Cultured

Substances

  • CCAAT-Enhancer-Binding Proteins
  • Carrier Proteins
  • DDIT3 protein, human
  • DNA-Binding Proteins
  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Heat-Shock Proteins
  • Intracellular Signaling Peptides and Proteins
  • Molecular Chaperones
  • Proteins
  • RNA, Messenger
  • Transcription Factors
  • Glutamine
  • Transcription Factor CHOP