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Article|09 Apr 2025|OPEN
CsPRMT5-mediated histone H4R3 dimethylation negatively regulates resistance to gray blight in tea plants (Camellia sinensis L.) 
Huanyun Peng1,2 , Yan Wang1,2 , Biying Zhu1 , Yuanrong Wang1 , Mengxue Han1 , Shupei Zhang1 and Tianyuan Yang1 , Fei Wang1 , , Zhaoliang Zhang,1 ,
1National Key Laboratory for Tea Plant Germplasm Innovation and Resource Utilization, Anhui Agricultural University, West 130 Changjiang Road, Hefei, Anhui 230036, China
2co-first author
*Corresponding author. E-mail: wfei@ahau.edu.cn,zhlzhang@ahau.edu.cn

Horticulture Research 12,
Article number: uhaf100 (2025)
doi: https://doi.org/10.1093/hr/uhaf100
Views: 2107

Received: 15 Dec 2024
Accepted: 24 Mar 2025
Published online: 09 Apr 2025

Abstract

Gray blight is a serious foliar disease that significantly threatens tea plant cultivation. Although dynamic histone methylation was reported in regulating plant immunity, the specific roles of this epigenetic modification in tea plant disease resistance have yet to be fully elucidated. This study demonstrates that the protein arginine methyltransferase CsPRMT5, which catalyzes the symmetric dimethylation of histone H4R3 (H4R3sme2), is involved in the tea plant response to gray blight. Transcription of CsPRMT5 and the level of histone H4R3 methylation in tea were downregulated following infection by the fungal pathogen Pseudopestalotiopsis (Ps). A negative correlation was observed between the resistance of tea plants to Ps and the expression level of CsPRMT5 across various cultivars. Downregulation of CsPRMT5 expression led to reduced H4R3sme2 levels, elevated expression of defense-related genes, and lower reactive oxygen species (ROS) production after Ps infection, thus enhancing pathogen resistance of tea. Furthermore, complementation of Atprmt5 mutant with CsPRMT5 restored the susceptibility to Ps infection in Arabidopsis. Chromatin Immunoprecipitation Sequencing (ChIP-seq)and Chromatin Immunoprecipitation quantitative PCR (ChIP-qPCR) analyses revealed that CsPRMT5 binds to defense-related genes, including CsMAPK3, and regulates their expression through H4R3sme2 modification. Collectively, the results indicate that CsPRMT5 negatively regulates the immune response to pathogens through repressing CsMAPK3 expression in tea plants.