The ribosomal protein Asc1/RACK1 is required for efficient translation of short mRNAs

Translation is a core cellular process carried out by a highly conserved macromolecular machine, the ribosome. There has been remarkable evolutionary adaptation of this machine through the addition of eukaryote-specific ribosomal proteins whose individual effects on ribosome function are largely unk...

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Main Authors: Mary K Thompson, Maria F Rojas-Duran, Paritosh Gangaramani, Wendy V Gilbert
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2016-04-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/11154
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spelling doaj-f9be7e3a161445d88edce4101bb41ca22021-05-05T00:22:19ZengeLife Sciences Publications LtdeLife2050-084X2016-04-01510.7554/eLife.11154The ribosomal protein Asc1/RACK1 is required for efficient translation of short mRNAsMary K Thompson0https://orcid.org/0000-0002-4947-6048Maria F Rojas-Duran1Paritosh Gangaramani2https://orcid.org/0000-0002-4893-8167Wendy V Gilbert3https://orcid.org/0000-0003-2807-9657Department of Biology, Massachusetts Institute of Technology, Cambridge, United StatesDepartment of Biology, Massachusetts Institute of Technology, Cambridge, United StatesDepartment of Biology, Massachusetts Institute of Technology, Cambridge, United StatesDepartment of Biology, Massachusetts Institute of Technology, Cambridge, United StatesTranslation is a core cellular process carried out by a highly conserved macromolecular machine, the ribosome. There has been remarkable evolutionary adaptation of this machine through the addition of eukaryote-specific ribosomal proteins whose individual effects on ribosome function are largely unknown. Here we show that eukaryote-specific Asc1/RACK1 is required for efficient translation of mRNAs with short open reading frames that show greater than average translational efficiency in diverse eukaryotes. ASC1 mutants in S. cerevisiae display compromised translation of specific functional groups, including cytoplasmic and mitochondrial ribosomal proteins, and display cellular phenotypes consistent with their gene-specific translation defects. Asc1-sensitive mRNAs are preferentially associated with the translational ‘closed loop’ complex comprised of eIF4E, eIF4G, and Pab1, and depletion of eIF4G mimics the translational defects of ASC1 mutants. Together our results reveal a role for Asc1/RACK1 in a length-dependent initiation mechanism optimized for efficient translation of genes with important housekeeping functions.https://elifesciences.org/articles/11154translationribosomeAsc1RACK1
collection DOAJ
language English
format Article
sources DOAJ
author Mary K Thompson
Maria F Rojas-Duran
Paritosh Gangaramani
Wendy V Gilbert
spellingShingle Mary K Thompson
Maria F Rojas-Duran
Paritosh Gangaramani
Wendy V Gilbert
The ribosomal protein Asc1/RACK1 is required for efficient translation of short mRNAs
eLife
translation
ribosome
Asc1
RACK1
author_facet Mary K Thompson
Maria F Rojas-Duran
Paritosh Gangaramani
Wendy V Gilbert
author_sort Mary K Thompson
title The ribosomal protein Asc1/RACK1 is required for efficient translation of short mRNAs
title_short The ribosomal protein Asc1/RACK1 is required for efficient translation of short mRNAs
title_full The ribosomal protein Asc1/RACK1 is required for efficient translation of short mRNAs
title_fullStr The ribosomal protein Asc1/RACK1 is required for efficient translation of short mRNAs
title_full_unstemmed The ribosomal protein Asc1/RACK1 is required for efficient translation of short mRNAs
title_sort ribosomal protein asc1/rack1 is required for efficient translation of short mrnas
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2016-04-01
description Translation is a core cellular process carried out by a highly conserved macromolecular machine, the ribosome. There has been remarkable evolutionary adaptation of this machine through the addition of eukaryote-specific ribosomal proteins whose individual effects on ribosome function are largely unknown. Here we show that eukaryote-specific Asc1/RACK1 is required for efficient translation of mRNAs with short open reading frames that show greater than average translational efficiency in diverse eukaryotes. ASC1 mutants in S. cerevisiae display compromised translation of specific functional groups, including cytoplasmic and mitochondrial ribosomal proteins, and display cellular phenotypes consistent with their gene-specific translation defects. Asc1-sensitive mRNAs are preferentially associated with the translational ‘closed loop’ complex comprised of eIF4E, eIF4G, and Pab1, and depletion of eIF4G mimics the translational defects of ASC1 mutants. Together our results reveal a role for Asc1/RACK1 in a length-dependent initiation mechanism optimized for efficient translation of genes with important housekeeping functions.
topic translation
ribosome
Asc1
RACK1
url https://elifesciences.org/articles/11154
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