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Iron-sulfur clusters are involved in post-translational arginylation
Eukaryotic arginylation is an essential post-translational modification that modulates protein stability and regulates protein half-life. Arginylation is catalyzed by a family of enzymes known as the arginyl-tRNA transferases (ATE1s), which are conserved across the eukaryotic domain. Despite their c...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884297/ https://www.ncbi.nlm.nih.gov/pubmed/36709327 http://dx.doi.org/10.1038/s41467-023-36158-z |
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author | Van, Verna Brown, Janae B. O’Shea, Corin R. Rosenbach, Hannah Mohamed, Ijaz Ejimogu, Nna-Emeka Bui, Toan S. Szalai, Veronika A. Chacón, Kelly N. Span, Ingrid Zhang, Fangliang Smith, Aaron T. |
author_facet | Van, Verna Brown, Janae B. O’Shea, Corin R. Rosenbach, Hannah Mohamed, Ijaz Ejimogu, Nna-Emeka Bui, Toan S. Szalai, Veronika A. Chacón, Kelly N. Span, Ingrid Zhang, Fangliang Smith, Aaron T. |
author_sort | Van, Verna |
collection | PubMed |
description | Eukaryotic arginylation is an essential post-translational modification that modulates protein stability and regulates protein half-life. Arginylation is catalyzed by a family of enzymes known as the arginyl-tRNA transferases (ATE1s), which are conserved across the eukaryotic domain. Despite their conservation and importance, little is known regarding the structure, mechanism, and regulation of ATE1s. In this work, we show that ATE1s bind a previously undiscovered [Fe-S] cluster that is conserved across evolution. We characterize the nature of this [Fe-S] cluster and find that the presence of the [Fe-S] cluster in ATE1 is linked to its arginylation activity, both in vitro and in vivo, and the initiation of the yeast stress response. Importantly, the ATE1 [Fe-S] cluster is oxygen-sensitive, which could be a molecular mechanism of the N-degron pathway to sense oxidative stress. Taken together, our data provide the framework of a cluster-based paradigm of ATE1 regulatory control. |
format | Online Article Text |
id | pubmed-9884297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98842972023-01-30 Iron-sulfur clusters are involved in post-translational arginylation Van, Verna Brown, Janae B. O’Shea, Corin R. Rosenbach, Hannah Mohamed, Ijaz Ejimogu, Nna-Emeka Bui, Toan S. Szalai, Veronika A. Chacón, Kelly N. Span, Ingrid Zhang, Fangliang Smith, Aaron T. Nat Commun Article Eukaryotic arginylation is an essential post-translational modification that modulates protein stability and regulates protein half-life. Arginylation is catalyzed by a family of enzymes known as the arginyl-tRNA transferases (ATE1s), which are conserved across the eukaryotic domain. Despite their conservation and importance, little is known regarding the structure, mechanism, and regulation of ATE1s. In this work, we show that ATE1s bind a previously undiscovered [Fe-S] cluster that is conserved across evolution. We characterize the nature of this [Fe-S] cluster and find that the presence of the [Fe-S] cluster in ATE1 is linked to its arginylation activity, both in vitro and in vivo, and the initiation of the yeast stress response. Importantly, the ATE1 [Fe-S] cluster is oxygen-sensitive, which could be a molecular mechanism of the N-degron pathway to sense oxidative stress. Taken together, our data provide the framework of a cluster-based paradigm of ATE1 regulatory control. Nature Publishing Group UK 2023-01-28 /pmc/articles/PMC9884297/ /pubmed/36709327 http://dx.doi.org/10.1038/s41467-023-36158-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Van, Verna Brown, Janae B. O’Shea, Corin R. Rosenbach, Hannah Mohamed, Ijaz Ejimogu, Nna-Emeka Bui, Toan S. Szalai, Veronika A. Chacón, Kelly N. Span, Ingrid Zhang, Fangliang Smith, Aaron T. Iron-sulfur clusters are involved in post-translational arginylation |
title | Iron-sulfur clusters are involved in post-translational arginylation |
title_full | Iron-sulfur clusters are involved in post-translational arginylation |
title_fullStr | Iron-sulfur clusters are involved in post-translational arginylation |
title_full_unstemmed | Iron-sulfur clusters are involved in post-translational arginylation |
title_short | Iron-sulfur clusters are involved in post-translational arginylation |
title_sort | iron-sulfur clusters are involved in post-translational arginylation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884297/ https://www.ncbi.nlm.nih.gov/pubmed/36709327 http://dx.doi.org/10.1038/s41467-023-36158-z |
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