Overexpression of ThMYB8 mediates salt stress tolerance by directly activating stress-responsive gene expression

被引:33
|
作者
Liu, Zhong-Yuan [1 ]
Li, Xin-Ping [1 ]
Zhang, Teng-Qian [1 ]
Wang, Yuan-Yuan [1 ]
Wang, Chao [1 ]
Gao, Cai-Qiu [1 ]
机构
[1] Northeast Forestry Univ, State Key Lab Tree Genet & Breeding, Harbin 150040, Peoples R China
基金
中国国家自然科学基金;
关键词
MBSI motif; RNA-seq; Salt stress; Tamarix hispida; MYB transcription factor; MYB TRANSCRIPTION FACTOR; R2R3; MYB; ABSCISIC-ACID; DROUGHT TOLERANCE; HIGH SALINITY; ARABIDOPSIS; COLD; CELL; HOMEOSTASIS; IDENTIFICATION;
D O I
10.1016/j.plantsci.2020.110668
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MYB transcription factors are important in abiotic stress responses; however, the detailed mechanisms are unclear. Tamarix hispida contains multiple MYB genes. The present study characterized T. hispida MYB8 (ThMYB8) during salt stress using transgenic T. hispida and Arabidopsis assays. ThMYB8 overexpression and ThMYB8 RNAi analysis demonstrated that ThMYB8 enhanced the salt stress tolerance. Transgenic Arabidopsis ectopic expression of ThMYB8 significantly increased root growth, fresh weight, and seed germination rate compared with that of the wild-type under salt stress. Physiological parameters analysis in T. hispida and Arabidopsis showed that ThMYB8 overexpressing plants had the lowest levels of O-2, H2O2, cell death, malondialdehyde, and electrolyte leakage. Overexpression of ThMYB8 regulated Na+ and K+ concentrations in plant tissues while maintaining K+/Na+ homeostasis. Analysis using qRT-PCR and ChIP-PCR identified possible downstream ThMYB8-regulated genes. ThMYB8 regulated the expression of ThCYP450-2 (cytochrome p450-2), Thltk (leucine-rich repeat transmembrane protein kinase), and ThTIP (aquaporin TIP) by binding to the MBSI motif ('CAACTG') in their promoters. The results indicated that ThMYB8 enhanced salt stress tolerance in T. hispida by regulating gene expression related to the activation of stress-associated physiological changes, such as enhanced reactive oxygen species scavenging capability, maintaining K+/Na+ homeostasis, and decreasing the malondialdehyde content and lipid peroxidation cell membranes.
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页数:11
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