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PMID: 28804493 Published · epublish English Journal Article

A Comprehensive Biophysical Model of Ion and Water Transport in Plant Roots. I. Clarifying the Roles of Endodermal Barriers in the Salt Stress Response.

Frontiers in plant science ·Vol. 8 ·2017-00-00 ·Pages 1326

Foster KJ, Miklavcic SJ

Abstract

In this paper, we present a detailed and comprehensive mathematical model of active and passive ion and water transport in plant roots. Two key features are the explicit consideration of the separate, but interconnected, apoplastic, and symplastic transport pathways for ions and water, and the inclusion of both active and passive ion transport mechanisms. The model is used to investigate the respective roles of the endodermal Casparian strip and suberin lamellae in the salt stress response of plant roots. While it is thought that these barriers influence different transport pathways, it has proven difficult to distinguish their separate functions experimentally. In particular, the specific role of the suberin lamellae has been unclear. A key finding based on our simulations was that the Casparian strip is essential in preventing excessive uptake of Na+ into the plant via apoplastic bypass, with a barrier efficiency that is reflected by a sharp gradient in the steady-state radial distribution of apoplastic Na+ across the barrier. Even more significantly, this function cannot be replaced by the action of membrane transporters. The simulations also demonstrated that the positive effect of the Casparian strip of controlling Na+ uptake, was somewhat offset by its contribution to the osmotic stress component: a more effective barrier increased the detrimental osmotic stress effect. In contrast, the suberin lamellae were found to play a relatively minor, even non-essential, role in the overall response to salt stress, with the presence of the suberin lamellae resulting in only a slight reduction in Na+ uptake. However, perhaps more significantly, the simulations identified a possible role of suberin lamellae in reducing plant energy requirements by acting as a physical barrier to preventing the passive leakage of Na+ into endodermal cells. The model results suggest that more and particular experimental attention should be paid to the properties of the Casparian strip when assessing the salt tolerance of different plant varieties and species. Indeed, the Casparian strip appears to be a more promising target for plant breeding and plant genetic engineering efforts than the suberin lamellae for the goal of improving salt tolerance.

Keywords
Casparian strip apoplastic and symplastic transport osmotic stress salt tolerance suberin lamellae
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Foster Kylie J
Phenomics and Bioinformatics Research Centre, School of Information Technology and Mathematical Sciences, University of South AustraliaMawson Lakes, SA, Australia.
Miklavcic Stanley J
Phenomics and Bioinformatics Research Centre, School of Information Technology and Mathematical Sciences, University of South AustraliaMawson Lakes, SA, Australia.
References (37)
37 references, click to expand
  1. Mechanisms of salinity tolerance.
    Annu Rev Plant Biol. 2008;59:651-81 PMID: 18444910
  2. Modeling Root Zone Effects on Preferred Pathways for the Passive Transport of Ions and Water in Plant Roots.
    Front Plant Sci. 2016 Jun 23;7:914 PMID: 27446144
  3. Understanding salinity responses and adopting 'omics-based' approaches to generate salinity tolerant cultivars of rice.
    Front Plant Sci. 2015 Sep 09;6:712 PMID: 26442026
  4. Toward a biophysical understanding of the salt stress response of individual plant cells.
    J Theor Biol. 2015 Nov 21;385:130-42 PMID: 26362103
  5. Zinc uptake and radial transport in roots of Arabidopsis thaliana: a modelling approach to understand accumulation.
    Ann Bot. 2013 Jul;112(2):369-80 PMID: 23258417
  6. The role of root apoplastic transport barriers in salt tolerance of rice (Oryza sativa L.).
    Planta. 2009 Jun;230(1):119-34 PMID: 19363620
  7. Cellular organisation of the Arabidopsis thaliana root.
    Development. 1993 Sep;119(1):71-84 PMID: 8275865
  8. Root apoplastic barriers block Na+ transport to shoots in rice (Oryza sativa L.).
    J Exp Bot. 2011 Aug;62(12):4215-28 PMID: 21558150
  9. Root suberin forms an extracellular barrier that affects water relations and mineral nutrition in Arabidopsis.
    PLoS Genet. 2009 May;5(5):e1000492 PMID: 19461889
  10. Regulation of expression of the vacuolar Na+/H+ antiporter gene AtNHX1 by salt stress and abscisic acid.
    Plant Mol Biol. 2002 Oct;50(3):543-50 PMID: 12369629
  11. Potassium transport and plant salt tolerance.
    Physiol Plant. 2008 Aug;133(4):651-69 PMID: 18724408
  12. Tissue-specific expression of Arabidopsis AKT1 gene is consistent with a role in K+ nutrition.
    Plant J. 1996 Feb;9(2):195-203 PMID: 8820606
  13. The potassium transporter AtHAK5 functions in K(+) deprivation-induced high-affinity K(+) uptake and AKT1 K(+) channel contribution to K(+) uptake kinetics in Arabidopsis roots.
    Plant Physiol. 2005 Mar;137(3):1105-14 PMID: 15734909
  14. K(+) channel profile and electrical properties of Arabidopsis root hairs.
    FEBS Lett. 2001 Nov 23;508(3):463-9 PMID: 11728473
  15. Modeling auxin-regulated development.
    Cold Spring Harb Perspect Biol. 2010 Feb;2(2):a001560 PMID: 20182620
  16. Radial transport of nutrients: the plant root as a polarized epithelium.
    Plant Physiol. 2014 Oct;166(2):528-37 PMID: 25136061
  17. Energy transduction in tonoplast vesicles from red beet (Beta vulgaris L.) storage tissue: H+/substrate stoichiometries for the H(+)-ATPase and H(+)-PPase.
    Arch Biochem Biophys. 1993 Feb 15;301(1):165-73 PMID: 8382906
  18. Adaptation of Root Function by Nutrient-Induced Plasticity of Endodermal Differentiation.
    Cell. 2016 Jan 28;164(3):447-59 PMID: 26777403
  19. Water and solute permeabilities of Arabidopsis roots in relation to the amount and composition of aliphatic suberin.
    J Exp Bot. 2011 Mar;62(6):1961-74 PMID: 21421706
  20. Auxin transport is sufficient to generate a maximum and gradient guiding root growth.
    Nature. 2007 Oct 25;449(7165):1008-13 PMID: 17960234
  21. Linking salinity stress tolerance with tissue-specific Na(+) sequestration in wheat roots.
    Front Plant Sci. 2015 Feb 20;6:71 PMID: 25750644
  22. Mathematical modelling of the uptake and transport of salt in plant roots.
    J Theor Biol. 2013 Nov 7;336:132-43 PMID: 23916880
  23. Sodium transport in plants: a critical review.
    New Phytol. 2011 Jan;189(1):54-81 PMID: 21118256
  24. In silico simulation modeling reveals the importance of the Casparian strip for efficient silicon uptake in rice roots.
    Plant Cell Physiol. 2015 Apr;56(4):631-9 PMID: 25673476
  25. Caspary's conductor.
    Proc Natl Acad Sci U S A. 2015 Aug 18;112(33):10084-5 PMID: 26283383
  26. The putative plasma membrane Na(+)/H(+) antiporter SOS1 controls long-distance Na(+) transport in plants.
    Plant Cell. 2002 Feb;14(2):465-77 PMID: 11884687
  27. A receptor-like kinase mutant with absent endodermal diffusion barrier displays selective nutrient homeostasis defects.
    Elife. 2014 Sep 16;3:e03115 PMID: 25233277
  28. The endodermis.
    Annu Rev Plant Biol. 2013;64:531-58 PMID: 23451777
  29. Casparian strip diffusion barrier in Arabidopsis is made of a lignin polymer without suberin.
    Proc Natl Acad Sci U S A. 2012 Jun 19;109(25):10101-6 PMID: 22665765
  30. On the competitive uptake and transport of ions through differentiated root tissues.
    J Theor Biol. 2014 Jan 7;340:1-10 PMID: 24036203
  31. Mathematical modeling and experimental validation of the spatial distribution of boron in the root of Arabidopsis thaliana identify high boron accumulation in the tip and predict a distinct root tip uptake function.
    Plant Cell Physiol. 2015 Apr;56(4):620-30 PMID: 25670713
  32. AKT1 and TRH1 are required during root hair elongation in Arabidopsis.
    J Exp Bot. 2003 Feb;54(383):781-8 PMID: 12554721
  33. Cell-specific localization of Na+ in roots of durum wheat and possible control points for salt exclusion.
    Plant Cell Environ. 2008 Nov;31(11):1565-74 PMID: 18702634
  34. Salinity-induced ion flux patterns from the excised roots of Arabidopsis sos mutants.
    Planta. 2005 Dec;222(6):1041-50 PMID: 16079998
  35. Identification and disruption of a plant shaker-like outward channel involved in K+ release into the xylem sap.
    Cell. 1998 Sep 4;94(5):647-55 PMID: 9741629
  36. Development of the Casparian strip in primary roots of maize under salt stress.
    Planta. 2004 May;219(1):41-7 PMID: 14986139
  37. Dirigent domain-containing protein is part of the machinery required for formation of the lignin-based Casparian strip in the root.
    Proc Natl Acad Sci U S A. 2013 Aug 27;110(35):14498-503 PMID: 23940370
Article Info
Journal
Frontiers in plant science
Abbr.
Front Plant Sci
ISSN
1664-462X
Published
2017-00-00
Epub
2017-00-28
Pages
1326
Language
English
Region
Switzerland
NLM ID
101568200
PMCID
PMC5532442
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