Evolutionary Changes in the Leishmania eIF4F Complex Involve Variations in the eIF4E–eIF4G Interactions

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Evolutionary Changes in the Leishmania eIF4F Complex Involve Variations in the eIF4E–eIF4G Interactions

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Title: Evolutionary Changes in the Leishmania eIF4F Complex Involve Variations in the eIF4E–eIF4G Interactions
Author: Yoffe, Yael; Léger, Mélissa; Zinoviev, Alexandra; Zuberek, Joanna; Darzynkiewicz, Edward; Shapira, Michal; Wagner, Gerhard

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Citation: Yoffe, Yael, Mélissa Léger, Alexandra Zinoviev, Joanna Zuberek, Edward Darzynkiewicz, Gerhard Wagner, and Michal Shapira. 2009. Evolutionary changes in the eIF4F complex involve variations in the eIF4E–eIF4G interactions. Nucleic Acids Research 37(10): 3243-3253.
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Abstract: Translation initiation in eukaryotes is mediated by assembly of the eIF4F complex over the m7GTP cap structure at the 5′-end of mRNAs. This requires an interaction between eIF4E and eIF4G, two eIF4F subunits. The Leishmania orthologs of eIF4E are structurally diverged from their higher eukaryote counterparts, since they have evolved to bind the unique trypanosomatid cap-4 structure. Here, we characterize a key eIF4G candidate from Leishmania parasites (LeishIF4G-3) that contains a conserved MIF4G domain. LeishIF4G-3 was found to coelute with the parasite eIF4F subunits from an m7GTP-Sepharose column and to bind directly to LeishIF4E. In higher eukaryotes the eIF4E-eIF4G interaction is based on a conserved peptide signature [Y(X4)Lϕ], where X is any amino acid and Φ is a hydrophobic residue. A parallel eIF4E-binding peptide was identified in LeishIF4G-3 (20-YPGFSLDE-27). However, the binding motif varies extensively: in addition to Y20 and L25, binding strictly requires the presence of F23, whereas the hydrophobic amino acid (Φ) is dispensable. The LeishIF4E–LeishIF4G-3 interaction was also confirmed by nuclear magnetic resonance (NMR) studies. In view of these diversities, the characterization of the parasite eIF4E–eIF4G interaction may not only serve as a novel target for inhibiting Leishmaniasis but also provide important insight for future drug discovery.
Published Version: doi:10.1093/nar/gkp190
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2691829/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:4725509

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