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Translation of small downstream ORFs enhances translation of canonical main open reading frames

In addition to canonical open reading frames (ORFs), thousands of translated small ORFs (containing less than 100 codons) have been identified in untranslated mRNA regions (UTRs) across eukaryotes. Small ORFs in 5′ UTRs (upstream (u)ORFs) often repress translation of the canonical ORF within the sam...

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Autores principales: Wu, Qiushuang, Wright, Matthew, Gogol, Madelaine M, Bradford, William D, Zhang, Ning, Bazzini, Ariel A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459409/
https://www.ncbi.nlm.nih.gov/pubmed/32744758
http://dx.doi.org/10.15252/embj.2020104763
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author Wu, Qiushuang
Wright, Matthew
Gogol, Madelaine M
Bradford, William D
Zhang, Ning
Bazzini, Ariel A
author_facet Wu, Qiushuang
Wright, Matthew
Gogol, Madelaine M
Bradford, William D
Zhang, Ning
Bazzini, Ariel A
author_sort Wu, Qiushuang
collection PubMed
description In addition to canonical open reading frames (ORFs), thousands of translated small ORFs (containing less than 100 codons) have been identified in untranslated mRNA regions (UTRs) across eukaryotes. Small ORFs in 5′ UTRs (upstream (u)ORFs) often repress translation of the canonical ORF within the same mRNA. However, the function of translated small ORFs in the 3′ UTRs (downstream (d)ORFs) is unknown. Contrary to uORFs, we find that translation of dORFs enhances translation of their corresponding canonical ORFs. This translation stimulatory effect of dORFs depends on the number of dORFs, but not the length or peptide they encode. We propose that dORFs represent a new, strong, and universal translation regulatory mechanism in vertebrates.
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spelling pubmed-74594092020-09-03 Translation of small downstream ORFs enhances translation of canonical main open reading frames Wu, Qiushuang Wright, Matthew Gogol, Madelaine M Bradford, William D Zhang, Ning Bazzini, Ariel A EMBO J Articles In addition to canonical open reading frames (ORFs), thousands of translated small ORFs (containing less than 100 codons) have been identified in untranslated mRNA regions (UTRs) across eukaryotes. Small ORFs in 5′ UTRs (upstream (u)ORFs) often repress translation of the canonical ORF within the same mRNA. However, the function of translated small ORFs in the 3′ UTRs (downstream (d)ORFs) is unknown. Contrary to uORFs, we find that translation of dORFs enhances translation of their corresponding canonical ORFs. This translation stimulatory effect of dORFs depends on the number of dORFs, but not the length or peptide they encode. We propose that dORFs represent a new, strong, and universal translation regulatory mechanism in vertebrates. John Wiley and Sons Inc. 2020-08-03 2020-09-01 /pmc/articles/PMC7459409/ /pubmed/32744758 http://dx.doi.org/10.15252/embj.2020104763 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Wu, Qiushuang
Wright, Matthew
Gogol, Madelaine M
Bradford, William D
Zhang, Ning
Bazzini, Ariel A
Translation of small downstream ORFs enhances translation of canonical main open reading frames
title Translation of small downstream ORFs enhances translation of canonical main open reading frames
title_full Translation of small downstream ORFs enhances translation of canonical main open reading frames
title_fullStr Translation of small downstream ORFs enhances translation of canonical main open reading frames
title_full_unstemmed Translation of small downstream ORFs enhances translation of canonical main open reading frames
title_short Translation of small downstream ORFs enhances translation of canonical main open reading frames
title_sort translation of small downstream orfs enhances translation of canonical main open reading frames
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459409/
https://www.ncbi.nlm.nih.gov/pubmed/32744758
http://dx.doi.org/10.15252/embj.2020104763
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