Overexpression of LOV KELCH PROTEIN 2 confers dehydration tolerance and is associated with enhanced expression of dehydration-inducible genes in Arabidopsis thaliana

被引:21
|
作者
Miyazaki, Yuji [1 ]
Abe, Hiroshi [2 ]
Takase, Tomoyuki [1 ]
Kobayashi, Masatomo [2 ]
Kiyosue, Tomohiro [1 ]
机构
[1] Gakushuin Univ, Dept Life Sci, Fac Sci, Toshima Ku, Tokyo 1718588, Japan
[2] RIKEN BioResource Ctr, Expt Plant Div, Dept Syst Biol, Tsukuba, Ibaraki 3050074, Japan
关键词
Arabidopsis; Dehydration-responsive element-binding factor (DREB); Dehydration tolerance; LOV KELCH PROTEIN 2 (LKP2); Stomatal aperture; DROUGHT STRESS TOLERANCE; TRANSCRIPTION FACTORS; CIRCADIAN CLOCK; TARGETED DEGRADATION; FUNCTIONAL-ANALYSIS; ZEITLUPE; PROTEIN; ABA; PATHWAYS; FKF1;
D O I
10.1007/s00299-015-1746-4
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The overexpression of LKP2 confers dehydration tolerance in Arabidopsis thaliana ; this is likely due to enhanced expression of dehydration-inducible genes and reduced stomatal opening. LOV KELCH PROTEIN 2 (LKP2) modulates the circadian rhythm and flowering time in plants. In this study, we observed that LKP2 overexpression enhanced dehydration tolerance in Arabidopsis. Microarray analysis demonstrated that expression of water deprivation-responsive genes was higher in the absence of dehydration stress in transgenic Arabidopsis plants expressing green fluorescent protein-tagged LKP2 (GFP-LKP2) than in control transgenic plants expressing GFP. After dehydration followed by rehydration, GFP-LKP2 plants developed more leaves and roots and exhibited higher survival rates than control plants. In the absence of dehydration stress, four dehydration-inducible genes, namely DREB1A, DREB1B, DREB1C, and RD29A, were expressed in GFP-LKP2 plants, whereas they were not expressed or were expressed at low levels in control plants. Under dehydration stress, the expression of DREB2B and RD29A peaked faster in the GFP-LKP2 plants than in control plants. The stomatal aperture of GFP-LKP2 plants was smaller than that of control plants. These results suggest that the dehydration tolerance of GFP-LKP2 plants is caused by upregulation of DREB1A-C/CBF1-3 and their downstream targets; restricted stomatal opening in the absence of dehydration stress also appears to contribute to the phenotype. The rapid and high expression of DREB2B and its downstream target genes also likely accounts for some features of the GFP-LKP2 phenotype. Our results suggest that LKP2 can be used for biotechnological applications not only to adjust the flowering time control but also to enhance dehydration tolerance.
引用
收藏
页码:843 / 852
页数:10
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