Mesophyll specific expression of a bacterial mercury transporter-based vacuolar sequestration machinery sufficiently enhances mercury tolerance of Arabidopsis

被引:2
|
作者
Uraguchi, Shimpei [1 ]
Ohshiro, Yuka [1 ]
Okuda, Mayu [1 ]
Kawakami, Shiho [1 ]
Yoneyama, Nene [1 ]
Tsuchiya, Yuta [1 ]
Nakamura, Ryosuke [1 ]
Takanezawa, Yasukazu [1 ]
Kiyono, Masako [1 ]
机构
[1] Kitasato Univ, Sch Pharm, Dept Publ Hlth, Tokyo, Japan
来源
基金
日本学术振兴会;
关键词
Arabidopsis; cell-type-specific promoter; MerC; mercury; mesophyll; molecular breeding; SNARE; vacuolar transporter; PHYTOCHELATIN SYNTHASE; CADMIUM ACCUMULATION; ION UPTAKE; RICE; PHYTOREMEDIATION; DETOXIFICATION; PROTEIN; SYP121; CELLS;
D O I
10.3389/fpls.2022.986600
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
We aimed to efficiently enhance plant Hg(II) tolerance by the transgenic approach utilizing a bacterial mercury transporter MerC, an Arabidopsis mesophyll specific promoter pRBCS1A, and a vacuolar membrane targeting syntaxin AtVAM3/SYP22. We generated two independent homozygous Arabidopsis pRBCS1A-TCV lines expressing mT-Sapphire-MerC-AtVAM3 under the control of pRBCS1A. Quantitative RT-PCR showed that the transgene was expressed specifically in shoots of pRBCS1A-TCV lines. Confocal analyses further demonstrated the leaf mesophyll specific expression of mT-Sapphire-MerC-AtVAM3. Confocal observation of the protoplast derived from the F1 plants of the pRBCS1A-TCV line and the tonoplast marker line p35S-GFP-delta TIP showed the tonoplast colocalization of mT-Sapphire-MerC-AtVAM3 and GFP-delta TIP. These results clearly demonstrated that mT-Sapphire-MerC-AtVAM3 expression in Arabidopsis is spatially regulated as designed at the transcript and the membrane trafficking levels. We then examined the Hg(II) tolerance of the pRBCS1A-TCV lines as well as the p35S-driven MerC-AtVAM3 expressing line p35S-CV under the various Hg(II) stress conditions. Short-term (12 d) Hg(II) treatment indicated the enhanced Hg(II) tolerance of both pRBCS1A-TCV and p35S-CV lines. The longer (3 weeks) Hg(II) treatment highlighted the better shoot growth of the transgenic plants compared to the wild-type Col-0 and the pRBCS1A-TCV lines were more tolerant to Hg(II) stress than the p35S-CV line. These results suggest that mesophyll-specific expression of MerC-AtVAM3 is sufficient or even better to enhance the Arabidopsis Hg(II) tolerance. The Hg accumulation in roots and shoots did not differ between the wild-type Col-0 and the MerC-AtVAM3 expressing plants, suggesting that the boosted Hg(II) tolerance of the transgenic lines would be attributed to vacuolar Hg-sequestration by the tonoplast-localized MerC. Further perspectives of the MerC-based plant engineering are also discussed.
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页数:10
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