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Co-evolution of large inverted repeats and G-quadruplex DNA in fungal mitochondria may facilitate mitogenome stability: the case of Malassezia

Mitogenomes are essential due to their contribution to cell respiration. Recently they have also been implicated in fungal pathogenicity mechanisms. Members of the basidiomycetous yeast genus Malassezia are an important fungal component of the human skin microbiome, linked to various skin diseases,...

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Autores principales: Christinaki, Anastasia C., Theelen, Bart, Zania, Alkmini, Coutinho, Selene Dall’ Acqua, Cabañes, Javier F., Boekhout, Teun, Kouvelis, Vassili N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113387/
https://www.ncbi.nlm.nih.gov/pubmed/37072481
http://dx.doi.org/10.1038/s41598-023-33486-4
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author Christinaki, Anastasia C.
Theelen, Bart
Zania, Alkmini
Coutinho, Selene Dall’ Acqua
Cabañes, Javier F.
Boekhout, Teun
Kouvelis, Vassili N.
author_facet Christinaki, Anastasia C.
Theelen, Bart
Zania, Alkmini
Coutinho, Selene Dall’ Acqua
Cabañes, Javier F.
Boekhout, Teun
Kouvelis, Vassili N.
author_sort Christinaki, Anastasia C.
collection PubMed
description Mitogenomes are essential due to their contribution to cell respiration. Recently they have also been implicated in fungal pathogenicity mechanisms. Members of the basidiomycetous yeast genus Malassezia are an important fungal component of the human skin microbiome, linked to various skin diseases, bloodstream infections, and they are increasingly implicated in gut diseases and certain cancers. In this study, the comparative analysis of Malassezia mitogenomes contributed to phylogenetic tree construction for all species. The mitogenomes presented significant size and gene order diversity which correlates to their phylogeny. Most importantly, they showed the inclusion of large inverted repeats (LIRs) and G-quadruplex (G4) DNA elements, rendering Malassezia mitogenomes a valuable test case for elucidating the evolutionary mechanisms responsible for this genome diversity. Both LIRs and G4s coexist and convergently evolved to provide genome stability through recombination. This mechanism is common in chloroplasts but, hitherto, rarely found in mitogenomes.
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spelling pubmed-101133872023-04-20 Co-evolution of large inverted repeats and G-quadruplex DNA in fungal mitochondria may facilitate mitogenome stability: the case of Malassezia Christinaki, Anastasia C. Theelen, Bart Zania, Alkmini Coutinho, Selene Dall’ Acqua Cabañes, Javier F. Boekhout, Teun Kouvelis, Vassili N. Sci Rep Article Mitogenomes are essential due to their contribution to cell respiration. Recently they have also been implicated in fungal pathogenicity mechanisms. Members of the basidiomycetous yeast genus Malassezia are an important fungal component of the human skin microbiome, linked to various skin diseases, bloodstream infections, and they are increasingly implicated in gut diseases and certain cancers. In this study, the comparative analysis of Malassezia mitogenomes contributed to phylogenetic tree construction for all species. The mitogenomes presented significant size and gene order diversity which correlates to their phylogeny. Most importantly, they showed the inclusion of large inverted repeats (LIRs) and G-quadruplex (G4) DNA elements, rendering Malassezia mitogenomes a valuable test case for elucidating the evolutionary mechanisms responsible for this genome diversity. Both LIRs and G4s coexist and convergently evolved to provide genome stability through recombination. This mechanism is common in chloroplasts but, hitherto, rarely found in mitogenomes. Nature Publishing Group UK 2023-04-18 /pmc/articles/PMC10113387/ /pubmed/37072481 http://dx.doi.org/10.1038/s41598-023-33486-4 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 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
Christinaki, Anastasia C.
Theelen, Bart
Zania, Alkmini
Coutinho, Selene Dall’ Acqua
Cabañes, Javier F.
Boekhout, Teun
Kouvelis, Vassili N.
Co-evolution of large inverted repeats and G-quadruplex DNA in fungal mitochondria may facilitate mitogenome stability: the case of Malassezia
title Co-evolution of large inverted repeats and G-quadruplex DNA in fungal mitochondria may facilitate mitogenome stability: the case of Malassezia
title_full Co-evolution of large inverted repeats and G-quadruplex DNA in fungal mitochondria may facilitate mitogenome stability: the case of Malassezia
title_fullStr Co-evolution of large inverted repeats and G-quadruplex DNA in fungal mitochondria may facilitate mitogenome stability: the case of Malassezia
title_full_unstemmed Co-evolution of large inverted repeats and G-quadruplex DNA in fungal mitochondria may facilitate mitogenome stability: the case of Malassezia
title_short Co-evolution of large inverted repeats and G-quadruplex DNA in fungal mitochondria may facilitate mitogenome stability: the case of Malassezia
title_sort co-evolution of large inverted repeats and g-quadruplex dna in fungal mitochondria may facilitate mitogenome stability: the case of malassezia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113387/
https://www.ncbi.nlm.nih.gov/pubmed/37072481
http://dx.doi.org/10.1038/s41598-023-33486-4
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