Cross species multi‐omics reveals cell wall sequestration and elevated global transcript abundance as mechanisms of boron tolerance in plants

Wang, Guannan; DiTusa, Sandra Feuer; Oh, Dong‐Ha; Herrmann, Achim D.; Mendoza‐Cozatl, David G.; O'Neill, Malcolm A.; Smith, Aaron P.; Dassanayake, Maheshi

doi:10.1111/nph.17295

Title: Cross species multi‐omics reveals cell wall sequestration and elevated global transcript abundance as mechanisms of boron tolerance in plants

Journal Article · 28 March 2021 · New Phytologist

DOI: https://doi.org/10.1111/nph.17295 · OSTI ID:1787150

^[1]; DiTusa, Sandra Feuer ^[1];

^[1]; Herrmann, Achim D. ^[2];

^[3];

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Department of Biological Sciences Louisiana State University Baton Rouge LA 70803 USA
Department of Geology &, Geophysics and Coastal Studies Institute Louisiana State University Baton Rouge LA 70803 USA
Division of Plant Sciences Interdisciplinary Plant Group Christopher S. Bond Life Sciences Center University of Missouri Columbia MO 65211 USA
Complex Carbohydrate Research Center The University of Georgia Athens GA 30602 USA

Summary Boron toxicity is a world‐wide problem for crops, yet we have a limited understanding of the genetic responses and adaptive mechanisms to this stress in plants. We employed a cross‐species comparison between boron stress‐sensitive Arabidopsis thaliana and its boron stress‐tolerant extremophyte relative Schrenkiella parvula , and a multi‐omics approach integrating genomics, transcriptomics, metabolomics and ionomics to assess plant responses and adaptations to boron stress. Schrenkiella parvula maintains lower concentrations of total boron and free boric acid than Arabidopsis when grown with excess boron. Schrenkiella parvula excludes excess boron more efficiently than Arabidopsis, which we propose is partly driven by SpBOR5, a boron transporter that we functionally characterize in this study. Both species use cell walls as a partial sink for excess boron. When accumulated in the cytoplasm, excess boron appears to interrupt RNA metabolism. The extremophyte S. parvula facilitates critical cellular processes while maintaining the pool of ribose‐containing compounds that can bind with boric acid. The S. parvula transcriptome is pre‐adapted to boron toxicity. It exhibits substantial overlaps with the Arabidopsis boron‐stress responsive transcriptome. Cell wall sequestration and increases in global transcript levels under excess boron conditions emerge as key mechanisms for sustaining plant growth under boron toxicity.

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Sponsoring Organization:: USDOE

OSTI ID:: 1787150

Journal Information:: New Phytologist, Journal Name: New Phytologist Vol. 230 Journal Issue: 5; ISSN 0028-646X

Publisher:: Wiley-BlackwellCopyright Statement

Country of Publication:: United Kingdom

Language:: English

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