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The origin and radiation of the phosphoprotein phosphatase (PPP) enzymes of Eukaryotes

Phosphoprotein phosphatase (PPP) enzymes are ubiquitous proteins involved in cellular signaling pathways and other functions. Here we have traced the origin of the PPP sequences of Eukaryotes and their radiation. Using a bacterial PPP Hidden Markov Model (HMM) we uncovered “BacterialPPP-Like” sequen...

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Autores principales: Kerk, David, Mattice, Jordan F., Valdés-Tresanco, Mario E., Noskov, Sergei Yu, Ng, Kenneth K.-S., Moorhead, Greg B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249667/
https://www.ncbi.nlm.nih.gov/pubmed/34211082
http://dx.doi.org/10.1038/s41598-021-93206-8
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author Kerk, David
Mattice, Jordan F.
Valdés-Tresanco, Mario E.
Noskov, Sergei Yu
Ng, Kenneth K.-S.
Moorhead, Greg B.
author_facet Kerk, David
Mattice, Jordan F.
Valdés-Tresanco, Mario E.
Noskov, Sergei Yu
Ng, Kenneth K.-S.
Moorhead, Greg B.
author_sort Kerk, David
collection PubMed
description Phosphoprotein phosphatase (PPP) enzymes are ubiquitous proteins involved in cellular signaling pathways and other functions. Here we have traced the origin of the PPP sequences of Eukaryotes and their radiation. Using a bacterial PPP Hidden Markov Model (HMM) we uncovered “BacterialPPP-Like” sequences in Archaea. A HMM derived from eukaryotic PPP enzymes revealed additional, unique sequences in Archaea and Bacteria that were more like the eukaryotic PPP enzymes then the bacterial PPPs. These sequences formed the basis of phylogenetic tree inference and sequence structural analysis allowing the history of these sequence types to be elucidated. Our phylogenetic tree data strongly suggest that eukaryotic PPPs ultimately arose from ancestors in the Asgard archaea. We have clarified the radiation of PPPs within Eukaryotes, substantially expanding the range of known organisms with PPP subtypes (Bsu1, PP7, PPEF/RdgC) previously thought to have a more restricted distribution. Surprisingly, sequences from the Methanosarcinaceae (Euryarchaeota) form a strongly supported sister group to eukaryotic PPPs in our phylogenetic analysis. This strongly suggests an intimate association between an Asgard ancestor and that of the Methanosarcinaceae. This is highly reminiscent of the syntrophic association recently demonstrated between the cultured Lokiarchaeal species Prometheoarchaeum and a methanogenic bacterial species.
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spelling pubmed-82496672021-07-06 The origin and radiation of the phosphoprotein phosphatase (PPP) enzymes of Eukaryotes Kerk, David Mattice, Jordan F. Valdés-Tresanco, Mario E. Noskov, Sergei Yu Ng, Kenneth K.-S. Moorhead, Greg B. Sci Rep Article Phosphoprotein phosphatase (PPP) enzymes are ubiquitous proteins involved in cellular signaling pathways and other functions. Here we have traced the origin of the PPP sequences of Eukaryotes and their radiation. Using a bacterial PPP Hidden Markov Model (HMM) we uncovered “BacterialPPP-Like” sequences in Archaea. A HMM derived from eukaryotic PPP enzymes revealed additional, unique sequences in Archaea and Bacteria that were more like the eukaryotic PPP enzymes then the bacterial PPPs. These sequences formed the basis of phylogenetic tree inference and sequence structural analysis allowing the history of these sequence types to be elucidated. Our phylogenetic tree data strongly suggest that eukaryotic PPPs ultimately arose from ancestors in the Asgard archaea. We have clarified the radiation of PPPs within Eukaryotes, substantially expanding the range of known organisms with PPP subtypes (Bsu1, PP7, PPEF/RdgC) previously thought to have a more restricted distribution. Surprisingly, sequences from the Methanosarcinaceae (Euryarchaeota) form a strongly supported sister group to eukaryotic PPPs in our phylogenetic analysis. This strongly suggests an intimate association between an Asgard ancestor and that of the Methanosarcinaceae. This is highly reminiscent of the syntrophic association recently demonstrated between the cultured Lokiarchaeal species Prometheoarchaeum and a methanogenic bacterial species. Nature Publishing Group UK 2021-07-01 /pmc/articles/PMC8249667/ /pubmed/34211082 http://dx.doi.org/10.1038/s41598-021-93206-8 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kerk, David
Mattice, Jordan F.
Valdés-Tresanco, Mario E.
Noskov, Sergei Yu
Ng, Kenneth K.-S.
Moorhead, Greg B.
The origin and radiation of the phosphoprotein phosphatase (PPP) enzymes of Eukaryotes
title The origin and radiation of the phosphoprotein phosphatase (PPP) enzymes of Eukaryotes
title_full The origin and radiation of the phosphoprotein phosphatase (PPP) enzymes of Eukaryotes
title_fullStr The origin and radiation of the phosphoprotein phosphatase (PPP) enzymes of Eukaryotes
title_full_unstemmed The origin and radiation of the phosphoprotein phosphatase (PPP) enzymes of Eukaryotes
title_short The origin and radiation of the phosphoprotein phosphatase (PPP) enzymes of Eukaryotes
title_sort origin and radiation of the phosphoprotein phosphatase (ppp) enzymes of eukaryotes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249667/
https://www.ncbi.nlm.nih.gov/pubmed/34211082
http://dx.doi.org/10.1038/s41598-021-93206-8
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