Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784906847977734144 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10013772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT chenhan thesetdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT fangyujie thesetdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT songwenrui thesetdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT shuhaidong thesetdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT lixi thesetdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT yewenwu thesetdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT wangyuanchao thesetdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT dongsuomeng thesetdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT chenhan setdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT fangyujie setdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT songwenrui setdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT shuhaidong setdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT lixi setdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT yewenwu setdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT wangyuanchao setdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae AT dongsuomeng setdomainproteinpskmt3regulateshistoneh3k36trimethylationandmodulateseffectorgeneexpressioninthesoybeanpathogenphytophthorasojae |