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Fusarium BP1 is a reader of H3K27 methylation
Histone H3 lysine 27 methylation catalyzed by polycomb repressive complex 2 (PRC2) is conserved from fungi to humans and represses gene transcription. However, the mechanism for recognition of methylated H3K27 remains unclear, especially in fungi. Here, we found that the bromo-adjacent homology (BAH...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501951/ https://www.ncbi.nlm.nih.gov/pubmed/34570240 http://dx.doi.org/10.1093/nar/gkab844 |
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author | Tang, Guangfei Yuan, Jianlong Wang, Jing Zhang, Yi-Zhe Xie, Si-Si Wang, Hongkai Tao, Zeng Liu, Huiquan Kistler, H Corby Zhao, Youfu Duan, Cheng-Guo Liu, Wende Ma, Zhonghua Chen, Yun |
author_facet | Tang, Guangfei Yuan, Jianlong Wang, Jing Zhang, Yi-Zhe Xie, Si-Si Wang, Hongkai Tao, Zeng Liu, Huiquan Kistler, H Corby Zhao, Youfu Duan, Cheng-Guo Liu, Wende Ma, Zhonghua Chen, Yun |
author_sort | Tang, Guangfei |
collection | PubMed |
description | Histone H3 lysine 27 methylation catalyzed by polycomb repressive complex 2 (PRC2) is conserved from fungi to humans and represses gene transcription. However, the mechanism for recognition of methylated H3K27 remains unclear, especially in fungi. Here, we found that the bromo-adjacent homology (BAH)-plant homeodomain (PHD) domain containing protein BAH–PHD protein 1 (BP1) is a reader of H3K27 methylation in the cereal fungal pathogen Fusarium graminearum. BP1 interacts with the core PRC2 component Suz12 and directly binds methylated H3K27. BP1 is distributed in a subset of genomic regions marked by H3K27me3 and co-represses gene transcription. The BP1 deletion mutant shows identical phenotypes on mycelial growth and virulence, as well as similar expression profiles of secondary metabolite genes to the strain lacking the H3K27 methyltransferase Kmt6. More importantly, BP1 can directly bind DNA through its PHD finger, which might increase nucleosome residence and subsequently reinforce transcriptional repression in H3K27me3-marked target regions. A phylogenetic analysis showed that BP1 orthologs are mainly conserved in fungi. Overall, our findings provide novel insights into the mechanism by which PRC2 mediates gene repression in fungi, which is distinct from the PRC1-PRC2 system in plants and mammals. |
format | Online Article Text |
id | pubmed-8501951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85019512021-10-12 Fusarium BP1 is a reader of H3K27 methylation Tang, Guangfei Yuan, Jianlong Wang, Jing Zhang, Yi-Zhe Xie, Si-Si Wang, Hongkai Tao, Zeng Liu, Huiquan Kistler, H Corby Zhao, Youfu Duan, Cheng-Guo Liu, Wende Ma, Zhonghua Chen, Yun Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Histone H3 lysine 27 methylation catalyzed by polycomb repressive complex 2 (PRC2) is conserved from fungi to humans and represses gene transcription. However, the mechanism for recognition of methylated H3K27 remains unclear, especially in fungi. Here, we found that the bromo-adjacent homology (BAH)-plant homeodomain (PHD) domain containing protein BAH–PHD protein 1 (BP1) is a reader of H3K27 methylation in the cereal fungal pathogen Fusarium graminearum. BP1 interacts with the core PRC2 component Suz12 and directly binds methylated H3K27. BP1 is distributed in a subset of genomic regions marked by H3K27me3 and co-represses gene transcription. The BP1 deletion mutant shows identical phenotypes on mycelial growth and virulence, as well as similar expression profiles of secondary metabolite genes to the strain lacking the H3K27 methyltransferase Kmt6. More importantly, BP1 can directly bind DNA through its PHD finger, which might increase nucleosome residence and subsequently reinforce transcriptional repression in H3K27me3-marked target regions. A phylogenetic analysis showed that BP1 orthologs are mainly conserved in fungi. Overall, our findings provide novel insights into the mechanism by which PRC2 mediates gene repression in fungi, which is distinct from the PRC1-PRC2 system in plants and mammals. Oxford University Press 2021-09-27 /pmc/articles/PMC8501951/ /pubmed/34570240 http://dx.doi.org/10.1093/nar/gkab844 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Tang, Guangfei Yuan, Jianlong Wang, Jing Zhang, Yi-Zhe Xie, Si-Si Wang, Hongkai Tao, Zeng Liu, Huiquan Kistler, H Corby Zhao, Youfu Duan, Cheng-Guo Liu, Wende Ma, Zhonghua Chen, Yun Fusarium BP1 is a reader of H3K27 methylation |
title | Fusarium BP1 is a reader of H3K27 methylation |
title_full | Fusarium BP1 is a reader of H3K27 methylation |
title_fullStr | Fusarium BP1 is a reader of H3K27 methylation |
title_full_unstemmed | Fusarium BP1 is a reader of H3K27 methylation |
title_short | Fusarium BP1 is a reader of H3K27 methylation |
title_sort | fusarium bp1 is a reader of h3k27 methylation |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501951/ https://www.ncbi.nlm.nih.gov/pubmed/34570240 http://dx.doi.org/10.1093/nar/gkab844 |
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