RapamycinFungusV1, Main, Exploration, bibRecord, 001A38

Eap1p, a novel eukaryotic translation initiation factor 4E-associated protein in Saccharomyces cerevisiae.

Identifieur interne : 001A38 ( Main/Exploration ); précédent : 001A37; suivant : 001A39

Eap1p, a novel eukaryotic translation initiation factor 4E-associated protein in Saccharomyces cerevisiae.

Auteurs : G P Cosentino [Canada] ; T. Schmelzle ; A. Haghighat ; S B Helliwell ; M N Hall ; N. Sonenberg

Source :

Molecular and cellular biology [ 0270-7306 ] ; 2000.

RBID : pubmed:10848587

Descripteurs français

English descriptors

KwdEn :
- Amino Acid Sequence (MeSH), Antifungal Agents (pharmacology), Binding, Competitive (MeSH), Drug Resistance, Microbial (MeSH), Eukaryotic Initiation Factor-4E (MeSH), Eukaryotic Initiation Factor-4G (MeSH), Fungal Proteins (drug effects), Fungal Proteins (genetics), Fungal Proteins (metabolism), Molecular Sequence Data (MeSH), Mutation (MeSH), Peptide Initiation Factors (genetics), Peptide Initiation Factors (metabolism), Phosphoproteins (metabolism), Protein Biosynthesis (MeSH), RNA Caps (MeSH), Saccharomyces cerevisiae (drug effects), Saccharomyces cerevisiae (genetics), Saccharomyces cerevisiae (metabolism), Signal Transduction (MeSH), Sirolimus (pharmacology), Temperature (MeSH).
MESH :
- chemical , drug effects : Fungal Proteins.
- chemical , genetics : Fungal Proteins, Peptide Initiation Factors.
- chemical , metabolism : Fungal Proteins, Peptide Initiation Factors, Phosphoproteins.
- chemical , pharmacology : Antifungal Agents, Sirolimus.
- drug effects : Saccharomyces cerevisiae.
- genetics : Saccharomyces cerevisiae.
- metabolism : Saccharomyces cerevisiae.
- Amino Acid Sequence, Binding, Competitive, Drug Resistance, Microbial, Eukaryotic Initiation Factor-4E, Eukaryotic Initiation Factor-4G, Molecular Sequence Data, Mutation, Protein Biosynthesis, RNA Caps, Signal Transduction, Temperature.

Abstract

Ribosome binding to eukaryotic mRNA is a multistep process which is mediated by the cap structure [m(7)G(5')ppp(5')N, where N is any nucleotide] present at the 5' termini of all cellular (with the exception of organellar) mRNAs. The heterotrimeric complex, eukaryotic initiation factor 4F (eIF4F), interacts directly with the cap structure via the eIF4E subunit and functions to assemble a ribosomal initiation complex on the mRNA. In mammalian cells, eIF4E activity is regulated in part by three related translational repressors (4E-BPs), which bind to eIF4E directly and preclude the assembly of eIF4F. No structural counterpart to 4E-BPs exists in the budding yeast, Saccharomyces cerevisiae. However, a functional homolog (named p20) has been described which blocks cap-dependent translation by a mechanism analogous to that of 4E-BPs. We report here on the characterization of a novel yeast eIF4E-associated protein (Eap1p) which can also regulate translation through binding to eIF4E. Eap1p shares limited homology to p20 in a region which contains the canonical eIF4E-binding motif. Deletion of this domain or point mutation abolishes the interaction of Eap1p with eIF4E. Eap1p competes with eIF4G (the large subunit of the cap-binding complex, eIF4F) and p20 for binding to eIF4E in vivo and inhibits cap-dependent translation in vitro. Targeted disruption of the EAP1 gene results in a temperature-sensitive phenotype and also confers partial resistance to growth inhibition by rapamycin. These data indicate that Eap1p plays a role in cell growth and implicates this protein in the TOR signaling cascade of S. cerevisiae.

DOI: 10.1128/mcb.20.13.4604-4613.2000
PubMed: 10848587
PubMed Central: PMC85860

Affiliations:

Links toward previous steps (curation, corpus...)

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Le document en format XML

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<term>Binding, Competitive (MeSH)</term>
<term>Drug Resistance, Microbial (MeSH)</term>
<term>Eukaryotic Initiation Factor-4E (MeSH)</term>
<term>Eukaryotic Initiation Factor-4G (MeSH)</term>
<term>Fungal Proteins (drug effects)</term>
<term>Fungal Proteins (genetics)</term>
<term>Fungal Proteins (metabolism)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Mutation (MeSH)</term>
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<term>Peptide Initiation Factors (metabolism)</term>
<term>Phosphoproteins (metabolism)</term>
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<term>Saccharomyces cerevisiae (genetics)</term>
<term>Saccharomyces cerevisiae (metabolism)</term>
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<term>Temperature (MeSH)</term>
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<term>Biosynthèse des protéines (MeSH)</term>
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<term>Données de séquences moléculaires (MeSH)</term>
<term>Facteur-4E d'initiation eucaryote (MeSH)</term>
<term>Facteur-4G d'initiation eucaryote (MeSH)</term>
<term>Facteurs initiation chaîne peptidique (génétique)</term>
<term>Facteurs initiation chaîne peptidique (métabolisme)</term>
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<term>Température (MeSH)</term>
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<term>Mutation</term>
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<term>Temperature</term>
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<term>Fixation compétitive</term>
<term>Mutation</term>
<term>Résistance microbienne aux médicaments</term>
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<front><div type="abstract" xml:lang="en">Ribosome binding to eukaryotic mRNA is a multistep process which is mediated by the cap structure [m(7)G(5')ppp(5')N, where N is any nucleotide] present at the 5' termini of all cellular (with the exception of organellar) mRNAs. The heterotrimeric complex, eukaryotic initiation factor 4F (eIF4F), interacts directly with the cap structure via the eIF4E subunit and functions to assemble a ribosomal initiation complex on the mRNA. In mammalian cells, eIF4E activity is regulated in part by three related translational repressors (4E-BPs), which bind to eIF4E directly and preclude the assembly of eIF4F. No structural counterpart to 4E-BPs exists in the budding yeast, Saccharomyces cerevisiae. However, a functional homolog (named p20) has been described which blocks cap-dependent translation by a mechanism analogous to that of 4E-BPs. We report here on the characterization of a novel yeast eIF4E-associated protein (Eap1p) which can also regulate translation through binding to eIF4E. Eap1p shares limited homology to p20 in a region which contains the canonical eIF4E-binding motif. Deletion of this domain or point mutation abolishes the interaction of Eap1p with eIF4E. Eap1p competes with eIF4G (the large subunit of the cap-binding complex, eIF4F) and p20 for binding to eIF4E in vivo and inhibits cap-dependent translation in vitro. Targeted disruption of the EAP1 gene results in a temperature-sensitive phenotype and also confers partial resistance to growth inhibition by rapamycin. These data indicate that Eap1p plays a role in cell growth and implicates this protein in the TOR signaling cascade of S. cerevisiae.</div>
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<Abstract><AbstractText>Ribosome binding to eukaryotic mRNA is a multistep process which is mediated by the cap structure [m(7)G(5')ppp(5')N, where N is any nucleotide] present at the 5' termini of all cellular (with the exception of organellar) mRNAs. The heterotrimeric complex, eukaryotic initiation factor 4F (eIF4F), interacts directly with the cap structure via the eIF4E subunit and functions to assemble a ribosomal initiation complex on the mRNA. In mammalian cells, eIF4E activity is regulated in part by three related translational repressors (4E-BPs), which bind to eIF4E directly and preclude the assembly of eIF4F. No structural counterpart to 4E-BPs exists in the budding yeast, Saccharomyces cerevisiae. However, a functional homolog (named p20) has been described which blocks cap-dependent translation by a mechanism analogous to that of 4E-BPs. We report here on the characterization of a novel yeast eIF4E-associated protein (Eap1p) which can also regulate translation through binding to eIF4E. Eap1p shares limited homology to p20 in a region which contains the canonical eIF4E-binding motif. Deletion of this domain or point mutation abolishes the interaction of Eap1p with eIF4E. Eap1p competes with eIF4G (the large subunit of the cap-binding complex, eIF4F) and p20 for binding to eIF4E in vivo and inhibits cap-dependent translation in vitro. Targeted disruption of the EAP1 gene results in a temperature-sensitive phenotype and also confers partial resistance to growth inhibition by rapamycin. These data indicate that Eap1p plays a role in cell growth and implicates this protein in the TOR signaling cascade of S. cerevisiae.</AbstractText>
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Eap1p, a novel eukaryotic translation initiation factor 4E-associated protein in Saccharomyces cerevisiae.

Eap1p, a novel eukaryotic translation initiation factor 4E-associated protein in Saccharomyces cerevisiae.

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