Phosphate deprivation‐induced changes in tomato are mediated by an interaction between brassinosteroid signaling and zinc

Author:

Demirer Gozde S.12,Gibson Donald J.1,Yue Xiaoyan13,Pan Kelly1,Elishav Eshel4,Khandal Hitaishi4,Horev Guy5,Tarkowská Danuše6ORCID,Cantó‐Pastor Alex1ORCID,Kong Shuyao1,Manzano Concepcion1,Maloof Julin N.1ORCID,Savaldi‐Goldstein Sigal4,Brady Siobhan M.1ORCID

Affiliation:

1. Department of Plant Biology and Genome Center University of California Davis Davis CA 95616 USA

2. Department of Chemical Engineering California Institute of Technology Pasadena CA 91125 USA

3. Department of Horticulture Zhejiang University Hangzhou Zhejiang 310058 China

4. Faculty of Biology Technion‐Israel Institute of Technology Haifa 3200003 Israel

5. Lorey I. Lokey Interdisciplinary Center for Life Sciences and Engineering Technion‐Israel Institute of Technology Haifa 3200003 Israel

6. Laboratory of Growth Regulators, Institute of Experimental Botany Czech Academy of Sciences and Palacky University Olomouc CZ‐78371 Czech Republic

Abstract

Summary Inorganic phosphate (Pi) is a necessary macronutrient for basic biological processes. Plants modulate their root system architecture (RSA) and cellular processes to adapt to Pi deprivation albeit with a growth penalty. Excess application of Pi fertilizer, on the contrary, leads to eutrophication and has a negative environmental impact. We compared RSA, root hair elongation, acid phosphatase activity, metal ion accumulation, and brassinosteroid hormone levels of Solanum lycopersicum (tomato) and Solanum pennellii, which is a wild relative of tomato, under Pi sufficiency and deficiency conditions to understand the molecular mechanism of Pi deprivation response in tomato. We showed that S. pennellii is partially insensitive to phosphate deprivation. Furthermore, it mounts a constitutive response under phosphate sufficiency. We demonstrate that activated brassinosteroid signaling through a tomato BZR1 ortholog gives rise to the same constitutive phosphate deficiency response, which is dependent on zinc overaccumulation. Collectively, these results reveal an additional strategy by which plants can adapt to phosphate starvation.

Funder

United States - Israel Binational Agricultural Research and Development Fund

European Regional Development Fund

Howard Hughes Medical Institute

National Science Foundation

Resnick Sustainability Institute for Science, Energy and Sustainability, California Institute of Technology

Publisher

Wiley

Subject

Plant Science,Physiology

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