GR1-like gene expression in Lycium chinense was regulated by cadmium-induced endogenous jasmonic acids accumulation

被引:18
|
作者
Ma, Zhigang [1 ,3 ]
An, Ting [2 ]
Zhu, Xuerui [2 ]
Ji, Jing [2 ]
Wang, Gang [2 ]
Guan, Chunfeng [2 ]
Jin, Chao [2 ]
Yi, Lingling [4 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Environm Sci & Engn, Tianjin 300072, Peoples R China
[3] Bengbu Med Coll, Bengbu 233000, Peoples R China
[4] Bengbu 2 High Sch, Bengbu 233000, Peoples R China
基金
中国国家自然科学基金;
关键词
Glutathione reductase; Lycium chinense; Cadmium; Jasmonic acids; Oxidative stress; ALLENE OXIDE CYCLASE; GLUTATHIONE METABOLIC GENES; OXIDATIVE STRESS; BRASSICA-JUNCEA; SALICYLIC-ACID; PHYSIOLOGICAL-RESPONSES; ARABIDOPSIS-THALIANA; METHYL JASMONATE; SALT TOLERANCE; NITRIC-OXIDE;
D O I
10.1007/s00299-017-2168-2
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The G1-like gene from the Lycium chinense was cloned and transferred into N. tabacum. Evidence showed that endogenous JA accumulation was crucial to LcGR gene expression in cadmium-stressed L. chinense. Glutathione reductase (GR) plays a vital role in glutathione-ascorbate metabolism and is a key enzyme in maintaining the redox state in plants. Jasmonic acids (JA) are important hormones regulating protective responses against bacteria and mechanic damage in plants. At present, the relationship between the endogenous JA accumulation, the glutathione (GSH) content and GR gene expression in plants under cadmium (Cd) stress has not been elucidated. This study primarily aims to explore their interconnected relations. First, we isolated the GR1-like gene from Lycium chinense (LcGR). Real-time PCR showed that gene LcGR and allene oxide cyclase (LcAOC) (a JA synthesis gene) expression in L. chinense plants was significantly enhanced by CdCl2 and reduced by CdCl2 cotreatment with 12,13-epoxy-octadecenoic acid (EOA), a JA synthesis inhibitor. Meanwhile, the JA content in plants strongly increased under Cd stress and decreased under Cd + EOA treatment, which was in accordance with expression pattern of LcAOC. The function of gene LcGR was confirmed in vitro with E. coli expression system. The subcellular localization in chloroplasts of LcGR gene was proved in Nicotiana tabacum leaves with transient transfection system of Agrobacterium tumefaciens. Furthermore, the overexpression of gene LcGR in the transgenic tabacum led to great Cd-tolerance and higher GSH accumulation. Overall, the results showed that the endogenous JA accumulation in Cd-stressed plants affects the GR expression which is crucial to the GSH accumulation and GSH-dependent tolerance to cadmium in LcGR transformants.
引用
收藏
页码:1457 / 1476
页数:20
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