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Repressor binding to a dorsal regulatory site traps human eIF4E in a high cap‐affinity state
Author(s) -
Ptushkina Marina,
von der Haar Tobias,
Karim Muhammad Manjurul,
Hughes John M.X.,
McCarthy John E.G.
Publication year - 1999
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/18.14.4068
Subject(s) - biology , repressor , binding site , eif4e , genetics , gene , transcription factor , translation (biology) , messenger rna
Eukaryotic translation initiation involves recognition of the 5′ end of cellular mRNA by the cap‐binding complex known as eukaryotic initiation factor 4F (eIF4F). Initiation is a key point of regulation in gene expression in response to mechanisms mediated by signal transduction pathways. We have investigated the molecular interactions underlying inhibition of human eIF4E function by regulatable repressors called 4E‐binding proteins (4E‐BPs). Two essential components of eIF4F are the cap‐binding protein eIF4E, and eIF4G, a multi‐functional protein that binds both eIF4E and other essential eIFs. We show that the 4E‐BPs 1 and 2 block the interaction between eIF4G and eIF4E by competing for binding to a dorsal site on eIF4E. Remarkably, binding of the 4E‐BPs at this dorsal site enhances cap‐binding via the ventral cap‐binding slot, thus trapping eIF4E in inactive complexes with high affinity for capped mRNA. The binding contacts and affinities for the interactions between 4E‐BP1/2 and eIF4E are distinct (estimated K d values of 10 −8 and 3×10 −9 for 4E‐BP1 and 2, respectively), and the differences in these properties are determined by three amino acids within an otherwise conserved motif. These data provide a quantitative framework for a new molecular model of translational regulation.