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A novel cytoprotective function for the DNA repair protein Ku in regulating p53 mRNA translation and function.
Lamaa, Assala; Le Bras, Morgane; Skuli, Nicolas; Britton, Sébastien; Frit, Philippe; Calsou, Patrick; Prats, Hervé; Cammas, Anne; Millevoi, Stefania.
Afiliação
  • Lamaa A; Cancer Research Center of Toulouse (CRCT), Inserm UMR 1037 Université Toulouse III-Paul Sabatier, Toulouse, France.
  • Le Bras M; Cancer Research Center of Toulouse (CRCT), Inserm UMR 1037 Université Toulouse III-Paul Sabatier, Toulouse, France.
  • Skuli N; Cancer Research Center of Toulouse (CRCT), Inserm UMR 1037 Université Toulouse III-Paul Sabatier, Toulouse, France.
  • Britton S; Institut de Pharmacologie et de Biologie Structurale, Université de Toulouse, CNRS UPS, France Equipe labellisée Ligue Nationale Contre le Cancer.
  • Frit P; Institut de Pharmacologie et de Biologie Structurale, Université de Toulouse, CNRS UPS, France Equipe labellisée Ligue Nationale Contre le Cancer.
  • Calsou P; Institut de Pharmacologie et de Biologie Structurale, Université de Toulouse, CNRS UPS, France Equipe labellisée Ligue Nationale Contre le Cancer.
  • Prats H; Cancer Research Center of Toulouse (CRCT), Inserm UMR 1037 Université Toulouse III-Paul Sabatier, Toulouse, France.
  • Cammas A; Cancer Research Center of Toulouse (CRCT), Inserm UMR 1037 Université Toulouse III-Paul Sabatier, Toulouse, France.
  • Millevoi S; Cancer Research Center of Toulouse (CRCT), Inserm UMR 1037 Université Toulouse III-Paul Sabatier, Toulouse, France stefania.millevoi@inserm.fr.
EMBO Rep ; 17(4): 508-18, 2016 04.
Article em En | MEDLINE | ID: mdl-26964895
ABSTRACT
Ku heterodimer is a DNA binding protein with a prominent role in DNA repair. Here, we investigate whether and how Ku impacts the DNA damage response by acting as a post-transcriptional regulator of gene expression. We show that Ku represses p53 protein synthesis and p53-mediated apoptosis by binding to a bulged stem-loop structure within the p53 5' UTR However, Ku-mediated translational repression of the p53 mRNA is relieved after genotoxic stress. The underlying mechanism involves Ku acetylation which disrupts Ku-p53 mRNA interactions. These results suggest that Ku-mediated repression of p53 mRNA translation constitutes a novel mechanism linking DNA repair and mRNA translation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biossíntese de Proteínas / Dano ao DNA / RNA Mensageiro / Proteína Supressora de Tumor p53 / Reparo do DNA / Autoantígeno Ku Limite: Humans Idioma: En Revista: EMBO Rep Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biossíntese de Proteínas / Dano ao DNA / RNA Mensageiro / Proteína Supressora de Tumor p53 / Reparo do DNA / Autoantígeno Ku Limite: Humans Idioma: En Revista: EMBO Rep Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França
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