Cargando…

The RNA-binding protein Fus directs translation of localized mRNAs in APC-RNP granules

RNA localization pathways direct numerous mRNAs to distinct subcellular regions and affect many physiological processes. In one such pathway the tumor-suppressor protein adenomatous polyposis coli (APC) targets RNAs to cell protrusions, forming APC-containing ribonucleoprotein complexes (APC-RNPs)....

Descripción completa

Detalles Bibliográficos
Autores principales: Yasuda, Kyota, Zhang, Huaye, Loiselle, David, Haystead, Timothy, Macara, Ian G., Mili, Stavroula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857475/
https://www.ncbi.nlm.nih.gov/pubmed/24297750
http://dx.doi.org/10.1083/jcb.201306058
_version_ 1782295161727877120
author Yasuda, Kyota
Zhang, Huaye
Loiselle, David
Haystead, Timothy
Macara, Ian G.
Mili, Stavroula
author_facet Yasuda, Kyota
Zhang, Huaye
Loiselle, David
Haystead, Timothy
Macara, Ian G.
Mili, Stavroula
author_sort Yasuda, Kyota
collection PubMed
description RNA localization pathways direct numerous mRNAs to distinct subcellular regions and affect many physiological processes. In one such pathway the tumor-suppressor protein adenomatous polyposis coli (APC) targets RNAs to cell protrusions, forming APC-containing ribonucleoprotein complexes (APC-RNPs). Here, we show that APC-RNPs associate with the RNA-binding protein Fus/TLS (fused in sarcoma/translocated in liposarcoma). Fus is not required for APC-RNP localization but is required for efficient translation of associated transcripts. Labeling of newly synthesized proteins revealed that Fus promotes translation preferentially within protrusions. Mutations in Fus cause amyotrophic lateral sclerosis (ALS) and the mutant protein forms inclusions that appear to correspond to stress granules. We show that overexpression or mutation of Fus results in formation of granules, which preferentially recruit APC-RNPs. Remarkably, these granules are not translationally silent. Instead, APC-RNP transcripts are translated within cytoplasmic Fus granules. These results unexpectedly show that translation can occur within stress-like granules. Importantly, they identify a new local function for cytoplasmic Fus with implications for ALS pathology.
format Online
Article
Text
id pubmed-3857475
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-38574752014-06-09 The RNA-binding protein Fus directs translation of localized mRNAs in APC-RNP granules Yasuda, Kyota Zhang, Huaye Loiselle, David Haystead, Timothy Macara, Ian G. Mili, Stavroula J Cell Biol Research Articles RNA localization pathways direct numerous mRNAs to distinct subcellular regions and affect many physiological processes. In one such pathway the tumor-suppressor protein adenomatous polyposis coli (APC) targets RNAs to cell protrusions, forming APC-containing ribonucleoprotein complexes (APC-RNPs). Here, we show that APC-RNPs associate with the RNA-binding protein Fus/TLS (fused in sarcoma/translocated in liposarcoma). Fus is not required for APC-RNP localization but is required for efficient translation of associated transcripts. Labeling of newly synthesized proteins revealed that Fus promotes translation preferentially within protrusions. Mutations in Fus cause amyotrophic lateral sclerosis (ALS) and the mutant protein forms inclusions that appear to correspond to stress granules. We show that overexpression or mutation of Fus results in formation of granules, which preferentially recruit APC-RNPs. Remarkably, these granules are not translationally silent. Instead, APC-RNP transcripts are translated within cytoplasmic Fus granules. These results unexpectedly show that translation can occur within stress-like granules. Importantly, they identify a new local function for cytoplasmic Fus with implications for ALS pathology. The Rockefeller University Press 2013-12-09 /pmc/articles/PMC3857475/ /pubmed/24297750 http://dx.doi.org/10.1083/jcb.201306058 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Yasuda, Kyota
Zhang, Huaye
Loiselle, David
Haystead, Timothy
Macara, Ian G.
Mili, Stavroula
The RNA-binding protein Fus directs translation of localized mRNAs in APC-RNP granules
title The RNA-binding protein Fus directs translation of localized mRNAs in APC-RNP granules
title_full The RNA-binding protein Fus directs translation of localized mRNAs in APC-RNP granules
title_fullStr The RNA-binding protein Fus directs translation of localized mRNAs in APC-RNP granules
title_full_unstemmed The RNA-binding protein Fus directs translation of localized mRNAs in APC-RNP granules
title_short The RNA-binding protein Fus directs translation of localized mRNAs in APC-RNP granules
title_sort rna-binding protein fus directs translation of localized mrnas in apc-rnp granules
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857475/
https://www.ncbi.nlm.nih.gov/pubmed/24297750
http://dx.doi.org/10.1083/jcb.201306058
work_keys_str_mv AT yasudakyota thernabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT zhanghuaye thernabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT loiselledavid thernabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT haysteadtimothy thernabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT macaraiang thernabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT milistavroula thernabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT yasudakyota rnabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT zhanghuaye rnabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT loiselledavid rnabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT haysteadtimothy rnabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT macaraiang rnabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules
AT milistavroula rnabindingproteinfusdirectstranslationoflocalizedmrnasinapcrnpgranules