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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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 |
work_keys_str_mv |
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1721476447474810880 |