Citrus CitNAC62 cooperates with CitWRKY1 to participate in citric acid degradation via up-regulation of CitAco3

被引:101
作者
Li, Shao-jia [1 ,2 ,3 ]
Yin, Xue-ren [1 ,2 ,3 ]
Wang, Wen-li [1 ,2 ]
Liu, Xiao-fen [1 ,2 ]
Zhang, Bo [1 ,2 ,3 ]
Chen, Kun-song [1 ,2 ,3 ]
机构
[1] Zhejiang Univ, Coll Agr & Biotechnol, Zijingang Campus, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Zhejiang Prov Key Lab Hort Plant Integrat Biol, Zijingang Campus, Hangzhou 310058, Zhejiang, Peoples R China
[3] Zhejiang Univ, State Agr Minist, Lab Hort Plant Growth Dev & Qual Improvement, Zijingang Campus, Hangzhou 310058, Zhejiang, Peoples R China
关键词
Aconitase; CitNAC62; citric acid; CitWRKY1; protein-protein interaction; transcriptional regulation; PRUNUS-AVIUM L; TRANSCRIPTION FACTOR; ORGANIC-ACIDS; TRANSIENT EXPRESSION; FRUIT-DEVELOPMENT; CHILLING INJURY; ARABIDOPSIS; GENE; BIOSYNTHESIS; ACCUMULATION;
D O I
10.1093/jxb/erx187
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Citric acid is the predominant organic acid of citrus fruit. Degradation of citric acid occurs during fruit development, influencing fruit acidity. Associations of CitAco3 transcripts and citric acid degradation have been reported for citrus fruit. Here, transient overexpression of CitAco3 significantly reduced the citric acid content of citrus leaves and fruits. Using dual luciferase assays, it was shown that CitNAC62 and CitWRKY1 could transactivate the promoter of CitAco3. Subcellular localization results showed that CitWRKY1 was located in the nucleus and CitNAC62 was not. Yeast two-hybrid analysis and bimolecular fluorescence complementation (BiFC) assays indicated that the two differently located transcription factors could interact with each other. Furthermore, BiFC showed that the protein-protein interaction occurred only in the nucleus, indicating the potential mobility of CitNAC62 in plant cells. A synergistic effect on citrate content was observed between CitNAC62 and CitWRKY1. Transient overexpression of CitNAC62 or CitWRKY1 led to significantly lower citrate content in citrus fruit. The combined expression of CitNAC62 and CitWRKY1 resulted in lower citrate content compared with the expression of CitNAC62 or CitWRKY1 alone. The transcript abundance of CitAco3 was consistent with the citrate content. Thus, we propose that a complex of CitWRKY1 and CitNAC62 contributes to citric acid degradation in citrus fruit, potentially via modulation of CitAco3.
引用
收藏
页码:3419 / 3426
页数:8
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