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Control of c-myc mRNA stability by IGF2BP1-associated cytoplasmic RNPs.
Weidensdorfer, Doreen; Stöhr, Nadine; Baude, Anne; Lederer, Marcell; Köhn, Marcel; Schierhorn, Angelika; Buchmeier, Sabine; Wahle, Elmar; Hüttelmaier, Stefan.
Afiliação
  • Weidensdorfer D; NBL3-NWG6 ZAMED, Department of Medicine, Martin Luther University Halle-Wittenberg, 06120 Halle, Germany.
RNA ; 15(1): 104-15, 2009 Jan.
Article em En | MEDLINE | ID: mdl-19029303
ABSTRACT
The RNA-binding protein IGF2BP1 (IGF-II mRNA binding protein 1) stabilizes the c-myc RNA by associating with the Coding Region instability Determinant (CRD). If and how other proteins cooperate with IGF2BP1 in promoting stabilization of the c-myc mRNA via the CRD remained elusive. Here, we identify various RNA-binding proteins that associate with IGF2BP1 in an RNA-dependent fashion. Four of these proteins (HNRNPU, SYNCRIP, YBX1, and DHX9) were essential to ensure stabilization of the c-myc mRNA via the CRD. These factors associate with IGF2BP1 in a CRD-dependent manner, co-distribute with IGF2BP1 in non-polysomal fractions comprising c-myc mRNA, and colocalize with IGF2BP1 in the cytoplasm. A selective shift of relative c-myc mRNA levels to the polysomal fraction is observed upon IGF2BP1 knockdown. These findings suggest that IGF2BP1 in complex with at least four proteins promotes CRD-mediated mRNA stabilization. Complex formation at the CRD presumably limits the transfer of c-myc mRNA to the polysomal fraction and subsequent translation-coupled decay.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ribonucleoproteínas / RNA Mensageiro / Proteínas Proto-Oncogênicas c-myc / Proteínas de Ligação a RNA / Citoplasma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ribonucleoproteínas / RNA Mensageiro / Proteínas Proto-Oncogênicas c-myc / Proteínas de Ligação a RNA / Citoplasma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2009 Tipo de documento: Article