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The SET domain protein PsKMT3 regulates histone H3K36 trimethylation and modulates effector gene expression in the soybean pathogen Phytophthora sojae

Plant pathogens secrete effector proteins to overcome host immunity and promote colonization. In oomycete plant pathogens, the expression of many effector genes is altered upon infection; however, the regulatory mechanisms are unclear. In this study, we identified a su(var)3–9, enhancer of zeste, an...

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Autores principales: Chen, Han, Fang, Yujie, Song, Wenrui, Shu, Haidong, Li, Xi, Ye, Wenwu, Wang, Yuanchao, Dong, Suomeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013772/
https://www.ncbi.nlm.nih.gov/pubmed/36748674
http://dx.doi.org/10.1111/mpp.13301
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author Chen, Han
Fang, Yujie
Song, Wenrui
Shu, Haidong
Li, Xi
Ye, Wenwu
Wang, Yuanchao
Dong, Suomeng
author_facet Chen, Han
Fang, Yujie
Song, Wenrui
Shu, Haidong
Li, Xi
Ye, Wenwu
Wang, Yuanchao
Dong, Suomeng
author_sort Chen, Han
collection PubMed
description Plant pathogens secrete effector proteins to overcome host immunity and promote colonization. In oomycete plant pathogens, the expression of many effector genes is altered upon infection; however, the regulatory mechanisms are unclear. In this study, we identified a su(var)3–9, enhancer of zeste, and trithorax (SET) domain protein‐encoding gene, PsKMT3, that was highly induced at early infection stages in Phytophthora sojae. Deletion of PsKMT3 led to asexual development and pathogenicity defects. Chromatin immunoprecipitation followed by sequencing (ChIP‐seq) and western blot analyses demonstrated that histone H3K36 trimethylation (H3K36me3) was significantly reduced genome‐wide in mutants. RNA‐seq analysis identified 374 genes encoding secreted proteins that were differentially expressed in pskmt3 at the mycelium stage. The significantly altered genes encompassed the RxLR (Arg‐x‐Lys‐Arg) effector gene family, including the essential effector genes Avh23, Avh181, Avh240, and Avh241. Transcriptome analysis at early infection stages showed misregulation of effector gene expression waves in pskmt3. H3K36me3 was directly and indirectly associated with RxLR effector gene activation. Our results reveal a role of a SET domain protein in regulating effector gene expression and modulating histone methylation in P. sojae.
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spelling pubmed-100137722023-03-15 The SET domain protein PsKMT3 regulates histone H3K36 trimethylation and modulates effector gene expression in the soybean pathogen Phytophthora sojae Chen, Han Fang, Yujie Song, Wenrui Shu, Haidong Li, Xi Ye, Wenwu Wang, Yuanchao Dong, Suomeng Mol Plant Pathol Original Articles Plant pathogens secrete effector proteins to overcome host immunity and promote colonization. In oomycete plant pathogens, the expression of many effector genes is altered upon infection; however, the regulatory mechanisms are unclear. In this study, we identified a su(var)3–9, enhancer of zeste, and trithorax (SET) domain protein‐encoding gene, PsKMT3, that was highly induced at early infection stages in Phytophthora sojae. Deletion of PsKMT3 led to asexual development and pathogenicity defects. Chromatin immunoprecipitation followed by sequencing (ChIP‐seq) and western blot analyses demonstrated that histone H3K36 trimethylation (H3K36me3) was significantly reduced genome‐wide in mutants. RNA‐seq analysis identified 374 genes encoding secreted proteins that were differentially expressed in pskmt3 at the mycelium stage. The significantly altered genes encompassed the RxLR (Arg‐x‐Lys‐Arg) effector gene family, including the essential effector genes Avh23, Avh181, Avh240, and Avh241. Transcriptome analysis at early infection stages showed misregulation of effector gene expression waves in pskmt3. H3K36me3 was directly and indirectly associated with RxLR effector gene activation. Our results reveal a role of a SET domain protein in regulating effector gene expression and modulating histone methylation in P. sojae. John Wiley and Sons Inc. 2023-02-07 /pmc/articles/PMC10013772/ /pubmed/36748674 http://dx.doi.org/10.1111/mpp.13301 Text en © 2023 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Chen, Han
Fang, Yujie
Song, Wenrui
Shu, Haidong
Li, Xi
Ye, Wenwu
Wang, Yuanchao
Dong, Suomeng
The SET domain protein PsKMT3 regulates histone H3K36 trimethylation and modulates effector gene expression in the soybean pathogen Phytophthora sojae
title The SET domain protein PsKMT3 regulates histone H3K36 trimethylation and modulates effector gene expression in the soybean pathogen Phytophthora sojae
title_full The SET domain protein PsKMT3 regulates histone H3K36 trimethylation and modulates effector gene expression in the soybean pathogen Phytophthora sojae
title_fullStr The SET domain protein PsKMT3 regulates histone H3K36 trimethylation and modulates effector gene expression in the soybean pathogen Phytophthora sojae
title_full_unstemmed The SET domain protein PsKMT3 regulates histone H3K36 trimethylation and modulates effector gene expression in the soybean pathogen Phytophthora sojae
title_short The SET domain protein PsKMT3 regulates histone H3K36 trimethylation and modulates effector gene expression in the soybean pathogen Phytophthora sojae
title_sort set domain protein pskmt3 regulates histone h3k36 trimethylation and modulates effector gene expression in the soybean pathogen phytophthora sojae
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013772/
https://www.ncbi.nlm.nih.gov/pubmed/36748674
http://dx.doi.org/10.1111/mpp.13301
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