Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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
_version_ 1784879688635645952
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
work_keys_str_mv AT vanverna ironsulfurclustersareinvolvedinposttranslationalarginylation
AT brownjanaeb ironsulfurclustersareinvolvedinposttranslationalarginylation
AT osheacorinr ironsulfurclustersareinvolvedinposttranslationalarginylation
AT rosenbachhannah ironsulfurclustersareinvolvedinposttranslationalarginylation
AT mohamedijaz ironsulfurclustersareinvolvedinposttranslationalarginylation
AT ejimogunnaemeka ironsulfurclustersareinvolvedinposttranslationalarginylation
AT buitoans ironsulfurclustersareinvolvedinposttranslationalarginylation
AT szalaiveronikaa ironsulfurclustersareinvolvedinposttranslationalarginylation
AT chaconkellyn ironsulfurclustersareinvolvedinposttranslationalarginylation
AT spaningrid ironsulfurclustersareinvolvedinposttranslationalarginylation
AT zhangfangliang ironsulfurclustersareinvolvedinposttranslationalarginylation
AT smithaaront ironsulfurclustersareinvolvedinposttranslationalarginylation