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Evolutionary reconstruction, nomenclature and functional meta-analysis of the Kiwellin protein family
Crop diseases caused by pathogens critically affect global food security and plant ecology. Pathogens are well adapted to their host plants and have developed sophisticated mechanisms allowing successful colonization. Plants in turn have taken measures to counteract pathogen attacks resulting in an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813671/ https://www.ncbi.nlm.nih.gov/pubmed/36618657 http://dx.doi.org/10.3389/fpls.2022.1034708 |
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author | Klemm, Paul Christ, Marvin Altegoer, Florian Freitag, Johannes Bange, Gert Lechner, Marcus |
author_facet | Klemm, Paul Christ, Marvin Altegoer, Florian Freitag, Johannes Bange, Gert Lechner, Marcus |
author_sort | Klemm, Paul |
collection | PubMed |
description | Crop diseases caused by pathogens critically affect global food security and plant ecology. Pathogens are well adapted to their host plants and have developed sophisticated mechanisms allowing successful colonization. Plants in turn have taken measures to counteract pathogen attacks resulting in an evolutionary arms race. Recent studies provided mechanistic insights into how two plant Kiwellin proteins from Zea mays mitigate the activity of the chorismate mutase Cmu1, a virulence factor secreted by the fungal pathogen Ustilago maydis during maize infection. Formerly identified as human allergens in kiwifruit, the biological function of Kiwellins is apparently linked to plant defense. We combined the analysis of proteome data with structural predictions to obtain a holistic overview of the Kiwellin protein family, that is subdivided into proteins with and without a N-terminal kissper domain. We found that Kiwellins are evolutionarily conserved in various plant species. At median five Kiwellin paralogs are encoded in each plant genome. Structural predictions revealed that Barwin-like proteins and Kiwellins cannot be discriminated purely at the sequence level. Our data shows that Kiwellins emerged in land plants (embryophyta) and are not present in fungi as suggested earlier. They evolved via three major duplication events that lead to clearly distinguishable subfamilies. We introduce a systematic Kiwellin nomenclature based on a detailed evolutionary reconstruction of this protein family. A meta-analysis of publicly available transcriptome data demonstrated that Kiwellins can be differentially regulated upon the interaction of plants with pathogens but also with symbionts. Furthermore, significant differences in Kiwellin expression levels dependent on tissues and cultivars were observed. In summary, our study sheds light on the evolution and regulation of a large protein family and provides a framework for a more detailed understanding of the molecular functions of Kiwellins. |
format | Online Article Text |
id | pubmed-9813671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98136712023-01-06 Evolutionary reconstruction, nomenclature and functional meta-analysis of the Kiwellin protein family Klemm, Paul Christ, Marvin Altegoer, Florian Freitag, Johannes Bange, Gert Lechner, Marcus Front Plant Sci Plant Science Crop diseases caused by pathogens critically affect global food security and plant ecology. Pathogens are well adapted to their host plants and have developed sophisticated mechanisms allowing successful colonization. Plants in turn have taken measures to counteract pathogen attacks resulting in an evolutionary arms race. Recent studies provided mechanistic insights into how two plant Kiwellin proteins from Zea mays mitigate the activity of the chorismate mutase Cmu1, a virulence factor secreted by the fungal pathogen Ustilago maydis during maize infection. Formerly identified as human allergens in kiwifruit, the biological function of Kiwellins is apparently linked to plant defense. We combined the analysis of proteome data with structural predictions to obtain a holistic overview of the Kiwellin protein family, that is subdivided into proteins with and without a N-terminal kissper domain. We found that Kiwellins are evolutionarily conserved in various plant species. At median five Kiwellin paralogs are encoded in each plant genome. Structural predictions revealed that Barwin-like proteins and Kiwellins cannot be discriminated purely at the sequence level. Our data shows that Kiwellins emerged in land plants (embryophyta) and are not present in fungi as suggested earlier. They evolved via three major duplication events that lead to clearly distinguishable subfamilies. We introduce a systematic Kiwellin nomenclature based on a detailed evolutionary reconstruction of this protein family. A meta-analysis of publicly available transcriptome data demonstrated that Kiwellins can be differentially regulated upon the interaction of plants with pathogens but also with symbionts. Furthermore, significant differences in Kiwellin expression levels dependent on tissues and cultivars were observed. In summary, our study sheds light on the evolution and regulation of a large protein family and provides a framework for a more detailed understanding of the molecular functions of Kiwellins. Frontiers Media S.A. 2022-12-22 /pmc/articles/PMC9813671/ /pubmed/36618657 http://dx.doi.org/10.3389/fpls.2022.1034708 Text en Copyright © 2022 Klemm, Christ, Altegoer, Freitag, Bange and Lechner https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Klemm, Paul Christ, Marvin Altegoer, Florian Freitag, Johannes Bange, Gert Lechner, Marcus Evolutionary reconstruction, nomenclature and functional meta-analysis of the Kiwellin protein family |
title | Evolutionary reconstruction, nomenclature and functional meta-analysis of the Kiwellin protein family |
title_full | Evolutionary reconstruction, nomenclature and functional meta-analysis of the Kiwellin protein family |
title_fullStr | Evolutionary reconstruction, nomenclature and functional meta-analysis of the Kiwellin protein family |
title_full_unstemmed | Evolutionary reconstruction, nomenclature and functional meta-analysis of the Kiwellin protein family |
title_short | Evolutionary reconstruction, nomenclature and functional meta-analysis of the Kiwellin protein family |
title_sort | evolutionary reconstruction, nomenclature and functional meta-analysis of the kiwellin protein family |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813671/ https://www.ncbi.nlm.nih.gov/pubmed/36618657 http://dx.doi.org/10.3389/fpls.2022.1034708 |
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