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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...

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Detalles Bibliográficos
Autores principales: Abbassi, Nour-el-Hana, Biela, Anna, Glatt, Sebastian, Lin, Ting-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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