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      Hormonal regulation of root hair growth and responses to the environment in Arabidopsis

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          Abstract

          This review presents a molecular framework for how phytohormones regulate normal root hair development and how this is affected by changes in the rhizosphere, to enable greater understanding of the specialized functions of root hairs and their developmental and environmental plasticity.

          Abstract

          The main functions of plant roots are water and nutrient uptake, soil anchorage, and interaction with soil-living biota. Root hairs, single cell tubular extensions of root epidermal cells, facilitate or enhance these functions by drastically enlarging the absorptive surface. Root hair development is constantly adapted to changes in the root’s surroundings, allowing for optimization of root functionality in heterogeneous soil environments. The underlying molecular pathway is the result of a complex interplay between position-dependent signalling and feedback loops. Phytohormone signalling interconnects this root hair signalling cascade with biotic and abiotic changes in the rhizosphere, enabling dynamic hormone-driven changes in root hair growth, density, length, and morphology. This review critically discusses the influence of the major plant hormones on root hair development, and how changes in rhizosphere properties impact on the latter.

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          Regulators of PP2C phosphatase activity function as abscisic acid sensors.

          The plant hormone abscisic acid (ABA) acts as a developmental signal and as an integrator of environmental cues such as drought and cold. Key players in ABA signal transduction include the type 2C protein phosphatases (PP2Cs) ABI1 and ABI2, which act by negatively regulating ABA responses. In this study, we identify interactors of ABI1 and ABI2 which we have named regulatory components of ABA receptor (RCARs). In Arabidopsis, RCARs belong to a family with 14 members that share structural similarity with class 10 pathogen-related proteins. RCAR1 was shown to bind ABA, to mediate ABA-dependent inactivation of ABI1 or ABI2 in vitro, and to antagonize PP2C action in planta. Other RCARs also mediated ABA-dependent regulation of ABI1 and ABI2, consistent with a combinatorial assembly of receptor complexes.
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            CHL1 functions as a nitrate sensor in plants.

            Ions serve as essential nutrients in higher plants and can also act as signaling molecules. Little is known about how plants sense changes in soil nutrient concentrations. Previous studies showed that T101-phosphorylated CHL1 is a high-affinity nitrate transporter, whereas T101-dephosphorylated CHL1 is a low-affinity transporter. In this study, analysis of an uptake- and sensing-decoupled mutant showed that the nitrate transporter CHL1 functions as a nitrate sensor. Primary nitrate responses in CHL1T101D and CHLT101A transgenic plants showed that phosphorylated and dephosphorylated CHL1 lead to a low- and high-level response, respectively. In vitro and in vivo studies showed that, in response to low nitrate concentrations, protein kinase CIPK23 can phosphorylate T101 of CHL1 to maintain a low-level primary response. Thus, CHL1 uses dual-affinity binding and a phosphorylation switch to sense a wide range of nitrate concentrations in the soil, thereby functioning as an ion sensor in higher plants. For a video summary of this article, see the PaperFlick file with the Supplemental Data available online.
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              Nitrate-regulated auxin transport by NRT1.1 defines a mechanism for nutrient sensing in plants.

              Nitrate is both a nitrogen source for higher plants and a signal molecule regulating their development. In Arabidopsis, the NRT1.1 nitrate transporter is crucial for nitrate signaling governing root growth, and has been proposed to act as a nitrate sensor. However, the sensing mechanism is unknown. Herein we show that NRT1.1 not only transports nitrate but also facilitates uptake of the phytohormone auxin. Moreover, nitrate inhibits NRT1.1-dependent auxin uptake, suggesting that transduction of nitrate signal by NRT1.1 is associated with a modification of auxin transport. Among other effects, auxin stimulates lateral root development. Mutation of NRT1.1 enhances both auxin accumulation in lateral roots and growth of these roots at low, but not high, nitrate concentration. Thus, we propose that NRT1.1 represses lateral root growth at low nitrate availability by promoting basipetal auxin transport out of these roots. This defines a mechanism connecting nutrient and hormone signaling during organ development. Copyright 2010 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                J Exp Bot
                J. Exp. Bot
                exbotj
                Journal of Experimental Botany
                Oxford University Press (UK )
                0022-0957
                1460-2431
                23 April 2020
                29 January 2020
                29 January 2020
                : 71
                : 8 , Special Issue: Plant Organ and Tip Growth
                : 2412-2427
                Affiliations
                [1 ] Integrated Molecular Plant Physiology Research, Department of Biology, University of Antwerp , Antwerp, Belgium
                [2 ] Plant Biochemistry and Biotechnology Lab, Department of Agriculture, Hellenic Mediterranean University , Stavromenos PC, Heraklion, Crete, Greece
                [3 ] University of Warwick , UK
                Author notes
                Author information
                http://orcid.org/0000-0003-0292-2095
                http://orcid.org/0000-0003-2300-6854
                Article
                eraa048
                10.1093/jxb/eraa048
                7178432
                31993645
                bec19de8-4959-44da-841f-6bd32d990029
                © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.

                History
                : 22 October 2019
                : 23 January 2020
                : 21 August 2020
                : 18 February 2020
                Page count
                Pages: 16
                Funding
                Funded by: University of Antwerp, DOI 10.13039/501100007660;
                Award ID: BOF-DOCPRO4
                Categories
                Review Papers
                AcademicSubjects/SCI01210

                Plant science & Botany
                arabidopsis,environment,hormone signalling,molecular pathway,root hairs,soil composition

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