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The histone code of the fungal genus Aspergillus uncovered by evolutionary and proteomic analyses

Chemical modifications of DNA and histone proteins impact the organization of chromatin within the nucleus. Changes in these modifications, catalysed by different chromatin-modifying enzymes, influence chromatin organization, which in turn is thought to impact the spatial and temporal regulation of...

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Autores principales: Zhang, Xin, Noberini, Roberta, Bonaldi, Tiziana, Collemare, Jerome, Seidl, Michael F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676040/
https://www.ncbi.nlm.nih.gov/pubmed/36129736
http://dx.doi.org/10.1099/mgen.0.000856
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author Zhang, Xin
Noberini, Roberta
Bonaldi, Tiziana
Collemare, Jerome
Seidl, Michael F.
author_facet Zhang, Xin
Noberini, Roberta
Bonaldi, Tiziana
Collemare, Jerome
Seidl, Michael F.
author_sort Zhang, Xin
collection PubMed
description Chemical modifications of DNA and histone proteins impact the organization of chromatin within the nucleus. Changes in these modifications, catalysed by different chromatin-modifying enzymes, influence chromatin organization, which in turn is thought to impact the spatial and temporal regulation of gene expression. While combinations of different histone modifications, the histone code, have been studied in several model species, we know very little about histone modifications in the fungal genus Aspergillus, whose members are generally well studied due to their importance as models in cell and molecular biology as well as their medical and biotechnological relevance. Here, we used phylogenetic analyses in 94 Aspergilli as well as other fungi to uncover the occurrence and evolutionary trajectories of enzymes and protein complexes with roles in chromatin modifications or regulation. We found that these enzymes and complexes are highly conserved in Aspergilli, pointing towards a complex repertoire of chromatin modifications. Nevertheless, we also observed few recent gene duplications or losses, highlighting Aspergillus species to further study the roles of specific chromatin modifications. SET7 (KMT6) and other components of PRC2 (Polycomb Repressive Complex 2), which is responsible for methylation on histone H3 at lysine 27 in many eukaryotes including fungi, are absent in Aspergilli as well as in closely related Penicillium species, suggesting that these lost the capacity for this histone modification. We corroborated our computational predictions by performing untargeted MS analysis of histone post-translational modifications in Aspergillus nidulans. This systematic analysis will pave the way for future research into the complexity of the histone code and its functional implications on genome architecture and gene regulation in fungi.
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spelling pubmed-96760402022-11-21 The histone code of the fungal genus Aspergillus uncovered by evolutionary and proteomic analyses Zhang, Xin Noberini, Roberta Bonaldi, Tiziana Collemare, Jerome Seidl, Michael F. Microb Genom Research Articles Chemical modifications of DNA and histone proteins impact the organization of chromatin within the nucleus. Changes in these modifications, catalysed by different chromatin-modifying enzymes, influence chromatin organization, which in turn is thought to impact the spatial and temporal regulation of gene expression. While combinations of different histone modifications, the histone code, have been studied in several model species, we know very little about histone modifications in the fungal genus Aspergillus, whose members are generally well studied due to their importance as models in cell and molecular biology as well as their medical and biotechnological relevance. Here, we used phylogenetic analyses in 94 Aspergilli as well as other fungi to uncover the occurrence and evolutionary trajectories of enzymes and protein complexes with roles in chromatin modifications or regulation. We found that these enzymes and complexes are highly conserved in Aspergilli, pointing towards a complex repertoire of chromatin modifications. Nevertheless, we also observed few recent gene duplications or losses, highlighting Aspergillus species to further study the roles of specific chromatin modifications. SET7 (KMT6) and other components of PRC2 (Polycomb Repressive Complex 2), which is responsible for methylation on histone H3 at lysine 27 in many eukaryotes including fungi, are absent in Aspergilli as well as in closely related Penicillium species, suggesting that these lost the capacity for this histone modification. We corroborated our computational predictions by performing untargeted MS analysis of histone post-translational modifications in Aspergillus nidulans. This systematic analysis will pave the way for future research into the complexity of the histone code and its functional implications on genome architecture and gene regulation in fungi. Microbiology Society 2022-09-21 /pmc/articles/PMC9676040/ /pubmed/36129736 http://dx.doi.org/10.1099/mgen.0.000856 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License.
spellingShingle Research Articles
Zhang, Xin
Noberini, Roberta
Bonaldi, Tiziana
Collemare, Jerome
Seidl, Michael F.
The histone code of the fungal genus Aspergillus uncovered by evolutionary and proteomic analyses
title The histone code of the fungal genus Aspergillus uncovered by evolutionary and proteomic analyses
title_full The histone code of the fungal genus Aspergillus uncovered by evolutionary and proteomic analyses
title_fullStr The histone code of the fungal genus Aspergillus uncovered by evolutionary and proteomic analyses
title_full_unstemmed The histone code of the fungal genus Aspergillus uncovered by evolutionary and proteomic analyses
title_short The histone code of the fungal genus Aspergillus uncovered by evolutionary and proteomic analyses
title_sort histone code of the fungal genus aspergillus uncovered by evolutionary and proteomic analyses
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676040/
https://www.ncbi.nlm.nih.gov/pubmed/36129736
http://dx.doi.org/10.1099/mgen.0.000856
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