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Article|11 Mar 2025|OPEN
CsWRKY17 enhances Al accumulation by promoting pectin deesterification in tea plant 
Danjuan Huang1,2 ,† , Jianqiang Ma2 ,† , Xun Chen1 , Hongjuan Wang1 , Rongrong Tan1 , Long Jiao1 , Jiedan Chen2 , and Yingxin Mao1 , , Liang Chen,2,3 ,
1Key Laboratory of Tea Resources Comprehensive Utilization of Ministry of Agriculture and Rural Affairs, Fruit and Tea Research Institute, Hubei Academy of Agricultural Sciences, 10 Nanhu Avenue, Hongshan District, Wuhan 430064, China
2Key Laboratory of Biology, Genetics and Breeding of Special Economic Animals and Plants, Ministry of Agriculture and Rural Affairs, Tea Research Institute of the Chinese Academy of Agricultural Sciences, 9 South Meiling Road, Xihu District, Hangzhou 310008, China
3Yunnan Key Laboratory of Tea Germplasm Conservation and Utilization in the Lancang River Basin, West Yunnan University, 2 Xuefu Road, Linxiang District, Lincang 677000, China
*Corresponding author. E-mail: chenjd@tricaas.com,maoyx1980@hbaas.com,liangchen@tricaas.com
Both authors contributed equally to the study.

Horticulture Research 12,
Article number: uhaf085 (2025)
doi: https://doi.org/10.1093/hr/uhaf085
Views: 1615

Received: 01 Aug 2024
Accepted: 03 Mar 2025
Published online: 11 Mar 2025

Abstract

The tea plant (Camellia sinensis) is a typical crop that accumulates aluminum (Al). Although the physiological mechanisms by which this occurs are well understood, their molecular mechanisms remain elusive. Here, an integrative approach combining quantitative trait locus (QTL) mapping of controlled hybridized populations and comparative transcriptomic analysis using samples treated with different Al concentrations was applied to identify candidate genes associated with Al accumulation in tea plants. Consequently, 41 candidate genes were selected using genome functional annotation of the qAl09 locus in the region of 35 256 594–57 378 817 bp on chromosome 7. Finally, a key gene, CsWRKY17, was identified as encoding a nucleus-localized transcription factor involved in regulating Al accumulation in tea plants, given the finding of a high correlation between its expression level and Al content in leaves. Overexpression of CsWRKY17 in Arabidopsis increased pectin deesterification, sensitivity to Al stress, and Al accumulation in leaves. Expression of the pectin methylesterase gene CsPME6 was found to be highly consistent with CsWRKY17 expression under various Al concentrations. In addition, experiments using a yeast monoclonal, electrophoresis mobility shift assay and dual-luciferase reporter (DLR) system confirmed that CsWRKY17 activated CsPME6 promoter activity. Antisense oligodeoxynucleotide silencing revealed a positive association between CsPME6 expression and Al accumulation in tea shoots. In conclusion, this study suggests that CsWRKY17 promoted the process of pectin deesterification by binding to the CsPME6 promoter, thereby enhancing Al enrichment in tea plants. Our findings lay the foundation for studying the precise mechanisms through which Al enriched in tea leaves.