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C8ORF88: A Novel eIF4E-Binding Protein
Translation initiation in eukaryotes is regulated at several steps, one of which involves the availability of the cap binding protein to participate in cap-dependent protein synthesis. Binding of eIF4E to translational repressors (eIF4E-binding proteins [4E-BPs]) suppresses translation and is used b...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10670996/ https://www.ncbi.nlm.nih.gov/pubmed/38003019 http://dx.doi.org/10.3390/genes14112076 |
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author | Pugsley, Lauren Naineni, Sai Kiran Amiri, Mehdi Yanagiya, Akiko Cencic, Regina Sonenberg, Nahum Pelletier, Jerry |
author_facet | Pugsley, Lauren Naineni, Sai Kiran Amiri, Mehdi Yanagiya, Akiko Cencic, Regina Sonenberg, Nahum Pelletier, Jerry |
author_sort | Pugsley, Lauren |
collection | PubMed |
description | Translation initiation in eukaryotes is regulated at several steps, one of which involves the availability of the cap binding protein to participate in cap-dependent protein synthesis. Binding of eIF4E to translational repressors (eIF4E-binding proteins [4E-BPs]) suppresses translation and is used by cells to link extra- and intracellular cues to protein synthetic rates. The best studied of these interactions involves repression of translation by 4E-BP1 upon inhibition of the PI3K/mTOR signaling pathway. Herein, we characterize a novel 4E-BP, C8ORF88, whose expression is predominantly restricted to early spermatids. C8ORF88:eIF4E interaction is dependent on the canonical eIF4E binding motif (4E-BM) present in other 4E-BPs. Whereas 4E-BP1:eIF4E interaction is dependent on the phosphorylation of 4E-BP1, these sites are not conserved in C8ORF88 indicating a different mode of regulation. |
format | Online Article Text |
id | pubmed-10670996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106709962023-11-14 C8ORF88: A Novel eIF4E-Binding Protein Pugsley, Lauren Naineni, Sai Kiran Amiri, Mehdi Yanagiya, Akiko Cencic, Regina Sonenberg, Nahum Pelletier, Jerry Genes (Basel) Article Translation initiation in eukaryotes is regulated at several steps, one of which involves the availability of the cap binding protein to participate in cap-dependent protein synthesis. Binding of eIF4E to translational repressors (eIF4E-binding proteins [4E-BPs]) suppresses translation and is used by cells to link extra- and intracellular cues to protein synthetic rates. The best studied of these interactions involves repression of translation by 4E-BP1 upon inhibition of the PI3K/mTOR signaling pathway. Herein, we characterize a novel 4E-BP, C8ORF88, whose expression is predominantly restricted to early spermatids. C8ORF88:eIF4E interaction is dependent on the canonical eIF4E binding motif (4E-BM) present in other 4E-BPs. Whereas 4E-BP1:eIF4E interaction is dependent on the phosphorylation of 4E-BP1, these sites are not conserved in C8ORF88 indicating a different mode of regulation. MDPI 2023-11-14 /pmc/articles/PMC10670996/ /pubmed/38003019 http://dx.doi.org/10.3390/genes14112076 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pugsley, Lauren Naineni, Sai Kiran Amiri, Mehdi Yanagiya, Akiko Cencic, Regina Sonenberg, Nahum Pelletier, Jerry C8ORF88: A Novel eIF4E-Binding Protein |
title | C8ORF88: A Novel eIF4E-Binding Protein |
title_full | C8ORF88: A Novel eIF4E-Binding Protein |
title_fullStr | C8ORF88: A Novel eIF4E-Binding Protein |
title_full_unstemmed | C8ORF88: A Novel eIF4E-Binding Protein |
title_short | C8ORF88: A Novel eIF4E-Binding Protein |
title_sort | c8orf88: a novel eif4e-binding protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10670996/ https://www.ncbi.nlm.nih.gov/pubmed/38003019 http://dx.doi.org/10.3390/genes14112076 |
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