Role of the translational repressor 4E-BP1 in the regulation of p21(Waf1/Cip1) expression by retinoids

Biochem Biophys Res Commun. 2008 Apr 18;368(4):983-9. doi: 10.1016/j.bbrc.2008.02.028. Epub 2008 Feb 15.

Abstract

The mechanisms by which retinoids regulate initiation of mRNA translation for proteins that mediate their biological effects are not known. We have previously shown that all-trans-retinoic acid (ATRA) induces mTOR-mediated activation of the p70 S6 kinase, suggesting the existence of a mechanism by which retinoids may regulate mRNA translation. We now demonstrate that treatment of acute promyelocytic leukemia (APL)-derived NB4 cells with ATRA results in dissociation of the translational repressor 4E-BP1 from the eukaryotic initiation factor eIF4E, and subsequent formation of eIF4G-eIF4E complexes. We also show that siRNA-mediated inhibition of 4E-BP1 expression enhances ATRA-dependent upregulation of p21(Waf1/Cip1), a protein that plays a key role in the induction of retinoid-dependent responses. Our data also establish that ATRA- or cis-RA-dependent p21(Waf1/Cip1) protein expression is enhanced in mouse embryonic fibroblasts with targeted disruption of the 4e-bp1 gene, in the absence of any effects on the transcriptional regulation of the p21(Waf1/Cip1) gene. Moreover, generation of ATRA- or cis-retinoic acid (cis-RA)-antiproliferative responses is enhanced in 4E-BP1 knockout cells. Altogether, these findings strongly suggest a key regulatory role for the translational repressor 4E-BP1 in the generation of retinoid-dependent functional responses.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing / physiology*
  • Animals
  • Cell Cycle Proteins
  • Cell Line, Tumor
  • Cyclin-Dependent Kinase Inhibitor p21 / biosynthesis*
  • Eukaryotic Initiation Factor-4E / metabolism
  • Gene Expression Regulation, Leukemic / drug effects
  • Humans
  • Leukemia, Promyelocytic, Acute
  • Mice
  • Mice, Knockout
  • Phosphoproteins / physiology*
  • Tretinoin / pharmacology*

Substances

  • Adaptor Proteins, Signal Transducing
  • CDKN1A protein, human
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p21
  • EIF4EBP1 protein, human
  • Eukaryotic Initiation Factor-4E
  • Phosphoproteins
  • Tretinoin