Poplar glutathione S-transferase PtrGSTF8 contributes to reactive oxygen species scavenging and salt tolerance

被引:2
|
作者
Song, Yushuang [1 ,2 ]
Yu, Keji [1 ,2 ]
Zhang, Shuwen [1 ]
Li, Yi [1 ,2 ]
Xu, Changwen [1 ,2 ]
Qian, Hongping [1 ,2 ]
Guo, Yayu [1 ,2 ]
Zhang, Xi [1 ,2 ]
Li, Ruili [1 ,2 ]
Dixon, Richard A. [3 ,4 ]
Lin, Jinxing [1 ,2 ]
机构
[1] Beijing Forestry Univ, Coll Biol Sci & Biotechnol, Beijing 100083, Peoples R China
[2] Beijing Forestry Univ, Inst Tree Dev & Genome Editing, Beijing 100083, Peoples R China
[3] Univ North Texas, BioDiscovery Inst, Denton, TX 76203 USA
[4] Univ North Texas, Dept Biol Sci, Denton, TX 76203 USA
基金
中国国家自然科学基金;
关键词
Glutathione S-Transferase; Poplar; PtrGSTF8; PtrMYB108; Salt tolerance; Transgenic tobacco; GENOME-WIDE IDENTIFICATION; SALINITY STRESS TOLERANCE; EXPRESSION ANALYSIS; GENE; ACCUMULATION; FAMILY;
D O I
10.1016/j.plaphy.2024.108766
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Glutathione S-transferases (GSTs) constitute a protein superfamily encoded by a large gene family and play a crucial role in plant growth and development. However, their precise functions in wood plant responses to abiotic stress are not fully understood. In this study, we isolated a Phi class glutathione S-transferase-encoding gene, PtrGSTF8, from poplar (Populus alba x P. glandulosa), which is significantly up-regulated under salt stress. Moreover, compared with wild-type (WT) plants, transgenic tobacco plants exhibited significant salt stress tolerance. Under salt stress, PtrGSTF8-overexpressing tobacco plants showed a significant increase in plant height and root length, and less accumulation of reactive oxygen species. In addition, these transgenic tobacco plants exhibited higher superoxide dismutase, peroxidase, and catalase activities and reduced malondialdehyde content compared with WT plants. Quantitative real-time PCR experiments showed that the overexpression of PtrGSTF8 increased the expression of numerous genes related to salt stress. Furthermore, PtrMYB108, a MYB transcription factor involved in salt resistance in poplar, was found to directly activate the promoter of PtrGSTF8, as demonstrated by yeast one-hybrid assays and luciferase complementation assays. Taken together, these findings suggest that poplar PtrGSTF8 contributes to enhanced salt tolerance and confers multiple growth advantages when overexpressed in tobacco.
引用
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页数:11
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