Transcription factor NtNAC56 regulates jasmonic acid-induced leaf senescence in tobacco

被引:4
作者
Chang, Wei [1 ]
Zhao, Huina [2 ]
Chen, Hongqiao [1 ]
Jiao, Guixiang [1 ]
Yu, Jing [2 ]
Wang, Bing [2 ]
Xia, Haiqian [2 ]
Meng, Boyu [1 ]
Li, Xiaodong [1 ]
Yu, Mengna [1 ]
Li, Shengting [1 ]
Qian, Mingchao [1 ]
Fan, Yonghai [1 ]
Zhang, Kai [1 ,3 ]
Lei, Bo [2 ]
Lu, Kun [1 ,3 ,4 ]
机构
[1] Southwest Univ, Coll Agron & Biotechnol, Chongqing 400715, Peoples R China
[2] Guizhou Acad Tobacco Sci, Mol Genet Key Lab China Tobacco, China Natl Tobacco Corp, Guiyang 550081, Peoples R China
[3] Minist Educ, Engn Res Ctr South Upland Agr, Chongqing 400715, Peoples R China
[4] Southwest Univ, Acad Agr Sci, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
GENE-EXPRESSION; DROUGHT; FAMILY; MAINTENANCE; REDUNDANCY; RESISTANCE; PCR;
D O I
10.1093/plphys/kiae116
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Leaf senescence is a vital aspect of plant physiology and stress responses and is induced by endogenous factors and environmental cues. The plant-specific NAC (NAM, ATAF1/2, CUC2) transcription factor family influences growth, development, and stress responses in Arabidopsis (Arabidopsis thaliana) and other species. However, the roles of NACs in tobacco (Nicotiana tabacum) leaf senescence are still unclear. Here, we report that NtNAC56 regulates leaf senescence in tobacco. Transgenic plants overexpressing NtNAC56 (NtNAC56-OE) showed induction of senescence-related genes and exhibited early senescence and lower chlorophyll content compared to wild-type (WT) plants and the Ntnac56-19 mutant. In addition, root development and seed germination were inhibited in the NtNAC56-OE lines. Transmission electron microscopy observations accompanied by physiological and biochemical assays revealed that NtNAC56 overexpression triggers chloroplast degradation and reactive oxygen species accumulation in tobacco leaves. Transcriptome analysis demonstrated that NtNAC56 activates leaf senescence-related genes and jasmonic acid (JA) biosynthesis pathway genes. In addition, the JA content of NtNAC56-OE plants was higher than in WT plants, and JA treatment induced NtNAC56 expression. We performed DNA affinity purification sequencing to identify direct targets of NtNAC56, among which we focused on LIPOXYGENASE 5 (NtLOX5), a key gene in JA biosynthesis. A dual-luciferase reporter assay and a yeast one-hybrid assay confirmed that NtNAC56 directly binds to the TTTCTT motif in the NtLOX5 promoter. Our results reveal a mechanism whereby NtNAC56 regulates JA-induced leaf senescence in tobacco and provide a strategy for genetically manipulating leaf senescence and plant growth.
引用
收藏
页码:1925 / 1940
页数:16
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