The grapevine NIP2;1 aquaporin is a silicon channel

Author:

Noronha Henrique12ORCID,Silva Angélica1,Mitani-Ueno Namiki3,Conde Carlos45,Sabir Farzana67ORCID,Prista Catarina7,Soveral Graça6,Isenring Paul8,Ma Jian Feng3ORCID,Bélanger Richard R9,Gerós Hernâni1210

Affiliation:

1. Centre of Molecular and Environmental Biology (CBMA), Department of Biology, University of Minho, Braga, Portugal

2. Centre for the Research and Technology of Agro-Environmental and Biological Sciences (CITAB), University of Trás-os-Montes e Alto Douro, Vila Real, Portugal

3. Institute of Plant Science and Resources, Okayama University, Chuo 2-20-1, Kurashiki, Japan

4. i3S, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal

5. IBMC, Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal

6. Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisboa, Portugal

7. LEAF, Linking Landscape, Environment, Agriculture and Food, and DRAT, Departamento de Recursos Biológicos, Ambiente e Território, Instituto Superior de Agronomia, Universidade de Lisboa, Tapada da Ajuda, Lisboa, Portugal

8. Nephrology Group, L’Hôtel-Dieu de Québec Institution, Department of Medicine, Faculty of Medicine, Université Laval, Québec, Québec, Canada

9. Département de Phytologie, Faculté des Sciences de l’Agriculture et de l’Alimentation (FSAA), Université Laval, Québec, Québec, Canada

10. Centre of Biological Engineering (CEB), Department of Engineering, University of Minho, Braga, Portugal

Abstract

Abstract Silicon (Si) supplementation has been shown to improve plant tolerance to different stresses, and its accumulation in the aerial organs is mediated by NIP2;1 aquaporins (Lsi channels) and Lsi2-type exporters in roots. In the present study, we tested the hypothesis that grapevine expresses a functional NIP2;1 that accounts for root Si uptake and, eventually, Si accumulation in leaves. Own-rooted grapevine cuttings of the cultivar Vinhão accumulated >0.2% Si (DW) in leaves when irrigated with 1.5 mM Si for 1 month, while Si was undetected in control leaves. Real-time PCR showed that VvNIP2;1 was highly expressed in roots and in green berries. The transient transformation of tobacco leaf epidermal cells mediated by Agrobacterium tumefaciens confirmed VvNIP2;1 localization at the plasma membrane. Transport experiments in oocytes showed that VvNIP2;1 mediates Si and arsenite uptake, whereas permeability studies revealed that VvNIP2;1 expressed in yeast is unable to transport water and glycerol. Si supplementation to pigmented grape cultured cells (cv. Gamay Freáux) had no impact on the total phenolic and anthocyanin content, or on the growth rate and VvNIP2;1 expression. Long-term experiments should help determine the extent of Si uptake over time and whether grapevine can benefit from Si fertilization.

Funder

Portuguese Foundation for Science and Technology

FCT and European

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

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