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A mechanism of translational repression by competition of Paip2 with eIF4G for poly(A) binding protein (PABP) binding
- Source :
- Proceedings of the National Academy of Sciences of the United States of America. 103(25)
- Publication Year :
- 2006
-
Abstract
- The eukaryotic mRNA 3′ poly(A) tail and the 5′ cap cooperate to synergistically enhance translation. This interaction is mediated by the cap-binding protein eIF4E, the poly(A) binding protein (PABP), and eIF4G, a scaffolding protein that bridges between eIF4E and PABP to bring about the circularization of the mRNA. The translational repressor, Paip2 (PABP-interacting protein 2), inhibits translation by promoting the dissociation of PABP from poly(A). Here we report on the existence of an alternative mechanism by which Paip2 inhibits translation by competing with eIF4G for binding to PABP. We demonstrate that Paip2 can abrogate the translational activity of PABP, which is tethered to the 3′ end of the mRNA. Thus, Paip2 can inhibit translation by a previously unrecognized mechanism, which is independent of its ability to disrupt PABP–poly(A) interaction.
- Subjects :
- RNA-binding protein
Biology
Binding, Competitive
Poly(A)-Binding Proteins
Cell Line
chemistry.chemical_compound
Poly(A)-binding protein
Protein biosynthesis
Messenger RNA
Multidisciplinary
EIF4G
Binding protein
EIF4E
food and beverages
RNA-Binding Proteins
Translation (biology)
Surface Plasmon Resonance
Biological Sciences
Cell biology
Kinetics
chemistry
Biochemistry
Protein Biosynthesis
biology.protein
Carrier Proteins
Eukaryotic Initiation Factor-4G
Protein Binding
Subjects
Details
- ISSN :
- 00278424
- Volume :
- 103
- Issue :
- 25
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Accession number :
- edsair.doi.dedup.....d764f5bc77104479632831f9ad74778a