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How Elongator Acetylates tRNA Bases
Elp3, the catalytic subunit of the eukaryotic Elongator complex, is a lysine acetyltransferase that acetylates the C5 position of wobble-base uridines (U(34)) in transfer RNAs (tRNAs). This Elongator-dependent RNA acetylation of anticodon bases affects the ribosomal translation elongation rates and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663514/ https://www.ncbi.nlm.nih.gov/pubmed/33152999 http://dx.doi.org/10.3390/ijms21218209 |
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author | Abbassi, Nour-el-Hana Biela, Anna Glatt, Sebastian Lin, Ting-Yu |
author_facet | Abbassi, Nour-el-Hana Biela, Anna Glatt, Sebastian Lin, Ting-Yu |
author_sort | Abbassi, Nour-el-Hana |
collection | PubMed |
description | Elp3, the catalytic subunit of the eukaryotic Elongator complex, is a lysine acetyltransferase that acetylates the C5 position of wobble-base uridines (U(34)) in transfer RNAs (tRNAs). This Elongator-dependent RNA acetylation of anticodon bases affects the ribosomal translation elongation rates and directly links acetyl-CoA metabolism to both protein synthesis rates and the proteome integrity. Of note, several human diseases, including various cancers and neurodegenerative disorders, correlate with the dysregulation of Elongator’s tRNA modification activity. In this review, we focus on recent findings regarding the structure of Elp3 and the role of acetyl-CoA during its unique modification reaction. |
format | Online Article Text |
id | pubmed-7663514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76635142020-11-14 How Elongator Acetylates tRNA Bases Abbassi, Nour-el-Hana Biela, Anna Glatt, Sebastian Lin, Ting-Yu Int J Mol Sci Review Elp3, the catalytic subunit of the eukaryotic Elongator complex, is a lysine acetyltransferase that acetylates the C5 position of wobble-base uridines (U(34)) in transfer RNAs (tRNAs). This Elongator-dependent RNA acetylation of anticodon bases affects the ribosomal translation elongation rates and directly links acetyl-CoA metabolism to both protein synthesis rates and the proteome integrity. Of note, several human diseases, including various cancers and neurodegenerative disorders, correlate with the dysregulation of Elongator’s tRNA modification activity. In this review, we focus on recent findings regarding the structure of Elp3 and the role of acetyl-CoA during its unique modification reaction. MDPI 2020-11-03 /pmc/articles/PMC7663514/ /pubmed/33152999 http://dx.doi.org/10.3390/ijms21218209 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Abbassi, Nour-el-Hana Biela, Anna Glatt, Sebastian Lin, Ting-Yu How Elongator Acetylates tRNA Bases |
title | How Elongator Acetylates tRNA Bases |
title_full | How Elongator Acetylates tRNA Bases |
title_fullStr | How Elongator Acetylates tRNA Bases |
title_full_unstemmed | How Elongator Acetylates tRNA Bases |
title_short | How Elongator Acetylates tRNA Bases |
title_sort | how elongator acetylates trna bases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663514/ https://www.ncbi.nlm.nih.gov/pubmed/33152999 http://dx.doi.org/10.3390/ijms21218209 |
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