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Deep Evolutionary History of the Phox and Bem1 (PB1) Domain Across Eukaryotes

Protein oligomerization is a fundamental process to build complex functional modules. Domains that facilitate the oligomerization process are diverse and widespread in nature across all kingdoms of life. One such domain is the Phox and Bem1 (PB1) domain, which is functionally well-studied in the ani...

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Autores principales: Mutte, Sumanth Kumar, Weijers, Dolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051960/
https://www.ncbi.nlm.nih.gov/pubmed/32123237
http://dx.doi.org/10.1038/s41598-020-60733-9
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author Mutte, Sumanth Kumar
Weijers, Dolf
author_facet Mutte, Sumanth Kumar
Weijers, Dolf
author_sort Mutte, Sumanth Kumar
collection PubMed
description Protein oligomerization is a fundamental process to build complex functional modules. Domains that facilitate the oligomerization process are diverse and widespread in nature across all kingdoms of life. One such domain is the Phox and Bem1 (PB1) domain, which is functionally well-studied in the animal kingdom. However, beyond animals, neither the origin nor the evolutionary patterns of PB1-containing proteins are understood. While PB1 domain proteins have been found in other kingdoms including plants, it is unclear how these relate to animal PB1 proteins. To address this question, we utilized large transcriptome datasets along with the proteomes of a broad range of species. We discovered eight PB1 domain-containing protein families in plants, along with four each in Protozoa and Fungi and three families in Chromista. Studying the deep evolutionary history of PB1 domains throughout eukaryotes revealed the presence of at least two, but likely three, ancestral PB1 copies in the Last Eukaryotic Common Ancestor (LECA). These three ancestral copies gave rise to multiple orthologues later in evolution. Analyzing the sequence and secondary structure properties of plant PB1 domains from all the eight families showed their common ubiquitin β-grasp fold, despite poor sequence identity. Tertiary structural models of these plant PB1 families, combined with Random Forest based classification, indicated family-specific differences attributed to the length of PB1 domain and the proportion of β-sheets. Thus, this study not only identifies novel PB1 families, but also provides an evolutionary basis to understand their diverse functional interactions.
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spelling pubmed-70519602020-03-06 Deep Evolutionary History of the Phox and Bem1 (PB1) Domain Across Eukaryotes Mutte, Sumanth Kumar Weijers, Dolf Sci Rep Article Protein oligomerization is a fundamental process to build complex functional modules. Domains that facilitate the oligomerization process are diverse and widespread in nature across all kingdoms of life. One such domain is the Phox and Bem1 (PB1) domain, which is functionally well-studied in the animal kingdom. However, beyond animals, neither the origin nor the evolutionary patterns of PB1-containing proteins are understood. While PB1 domain proteins have been found in other kingdoms including plants, it is unclear how these relate to animal PB1 proteins. To address this question, we utilized large transcriptome datasets along with the proteomes of a broad range of species. We discovered eight PB1 domain-containing protein families in plants, along with four each in Protozoa and Fungi and three families in Chromista. Studying the deep evolutionary history of PB1 domains throughout eukaryotes revealed the presence of at least two, but likely three, ancestral PB1 copies in the Last Eukaryotic Common Ancestor (LECA). These three ancestral copies gave rise to multiple orthologues later in evolution. Analyzing the sequence and secondary structure properties of plant PB1 domains from all the eight families showed their common ubiquitin β-grasp fold, despite poor sequence identity. Tertiary structural models of these plant PB1 families, combined with Random Forest based classification, indicated family-specific differences attributed to the length of PB1 domain and the proportion of β-sheets. Thus, this study not only identifies novel PB1 families, but also provides an evolutionary basis to understand their diverse functional interactions. Nature Publishing Group UK 2020-03-02 /pmc/articles/PMC7051960/ /pubmed/32123237 http://dx.doi.org/10.1038/s41598-020-60733-9 Text en © The Author(s) 2020 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/.
spellingShingle Article
Mutte, Sumanth Kumar
Weijers, Dolf
Deep Evolutionary History of the Phox and Bem1 (PB1) Domain Across Eukaryotes
title Deep Evolutionary History of the Phox and Bem1 (PB1) Domain Across Eukaryotes
title_full Deep Evolutionary History of the Phox and Bem1 (PB1) Domain Across Eukaryotes
title_fullStr Deep Evolutionary History of the Phox and Bem1 (PB1) Domain Across Eukaryotes
title_full_unstemmed Deep Evolutionary History of the Phox and Bem1 (PB1) Domain Across Eukaryotes
title_short Deep Evolutionary History of the Phox and Bem1 (PB1) Domain Across Eukaryotes
title_sort deep evolutionary history of the phox and bem1 (pb1) domain across eukaryotes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051960/
https://www.ncbi.nlm.nih.gov/pubmed/32123237
http://dx.doi.org/10.1038/s41598-020-60733-9
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