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      Xylem K + loading modulates K + and Cs + absorption and distribution in Arabidopsis under K +-limited conditions

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          Abstract

          Potassium (K +) is an essential macronutrient for plant growth. The transcriptional regulation of K + transporter genes is one of the key mechanisms by which plants respond to K + deficiency. Among the HAK/KUP/KT transporter family, HAK5, a high-affinity K + transporter, is essential for root K + uptake under low external K + conditions. HAK5 expression in the root is highly induced by low external K + concentration. While the molecular mechanisms of HAK5 regulation have been extensively studied, it remains unclear how plants sense and coordinates K + uptake and translocation in response to changing environmental conditions. Using skor mutants, which have a defect in root-to-shoot K + translocation, we have been able to determine how the internal K + status affects the expression of HAK5. In skor mutant roots, under K + deficiency, HAK5 expression was lower than in wild-type although the K + concentration in roots was not significantly different. These results reveal that HAK5 is not only regulated by external K + conditions but it is also regulated by internal K + levels, which is in agreement with recent findings. Additionally, HAK5 plays a major role in the uptake of Cs + in roots. Therefore, studying Cs + in roots and having more detailed information about its uptake and translocation in the plant would be valuable. Radioactive tracing experiments revealed not only a reduction in the uptake of 137Cs + and 42K +in skor mutants compared to wild-type but also a different distribution of 137Cs + and 42K + in tissues. In order to gain insight into the translocation, accumulation, and repartitioning of both K + and Cs + in plants, long-term treatment and split root experiments were conducted with the stable isotopes 133Cs + and 85Rb +. Finally, our findings show that the K + distribution in plant tissues regulates root uptake of K + and Cs + similarly, depending on HAK5; however, the translocation and accumulation of the two elements are different.

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          Most cited references58

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          Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

          The two most commonly used methods to analyze data from real-time, quantitative PCR experiments are absolute quantification and relative quantification. Absolute quantification determines the input copy number, usually by relating the PCR signal to a standard curve. Relative quantification relates the PCR signal of the target transcript in a treatment group to that of another sample such as an untreated control. The 2(-Delta Delta C(T)) method is a convenient way to analyze the relative changes in gene expression from real-time quantitative PCR experiments. The purpose of this report is to present the derivation, assumptions, and applications of the 2(-Delta Delta C(T)) method. In addition, we present the derivation and applications of two variations of the 2(-Delta Delta C(T)) method that may be useful in the analysis of real-time, quantitative PCR data. Copyright 2001 Elsevier Science (USA).
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            Potassium transport and signaling in higher plants.

            Yi Wang, Hua Wu (2012)
            As one of the most important mineral nutrient elements, potassium (K(+)) participates in many plant physiological processes and determines the yield and quality of crop production. In this review, we summarize K(+) signaling processes and K(+) transport regulation in higher plants, especially in plant responses to K(+)-deficiency stress. Plants perceive external K(+) fluctuations and generate the initial K(+) signal in root cells. This signal is transduced into the cytoplasm and encoded as Ca(2+) and reactive oxygen species signaling. K(+)-deficiency-induced signals are subsequently decoded by cytoplasmic sensors, which regulate the downstream transcriptional and posttranslational responses. Eventually, plants produce a series of adaptive events in both physiological and morphological alterations that help them survive K(+) deficiency.
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              Design and validation of a tool for neurite tracing and analysis in fluorescence microscopy images.

              For the investigation of the molecular mechanisms involved in neurite outgrowth and differentiation, accurate and reproducible segmentation and quantification of neuronal processes are a prerequisite. To facilitate this task, we developed a semiautomatic neurite tracing technique. This article describes the design and validation of the technique. The technique was compared to fully manual delineation. Four observers repeatedly traced selected neurites in 20 fluorescence microscopy images of cells in culture, using both methods. Accuracy and reproducibility were determined by comparing the tracings to high-resolution reference tracings, using two error measures. Labor intensiveness was measured in numbers of mouse clicks required. The significance of the results was determined by a Student t-test and by analysis of variance. Both methods slightly underestimated the true neurite length, but the differences were not unanimously significant. The average deviation from the true neurite centerline was a factor 2.6 smaller with the developed technique compared to fully manual tracing. Intraobserver variability in the respective measures was reduced by a factor 6.0 and 23.2. Interobserver variability was reduced by a factor 2.4 and 8.8, respectively, and labor intensiveness by a factor 3.3. Providing similar accuracy in measuring neurite length, significantly improved accuracy in neurite centerline extraction, and significantly improved reproducibility and reduced labor intensiveness, the developed technique may replace fully manual tracing methods. Copyright 2004 Wiley-Liss, Inc.
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                Author and article information

                Contributors
                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                22 September 2023
                2023
                : 14
                : 1040118
                Affiliations
                [1] 1 AixMarseille University, French Alternative Energies and Atomic Energy Commission (CEA), National Center for Scientific Research (CNRS), Bioscience and Biotechnology Institute of Aix-Marseille (BIAM) , Saint-Paul Lez Durance, France
                [2] 2 Faculty of Life and Environmental Sciences University of Tsukuba , Tsukuba, Ibaraki, Japan
                [3] 3 Institute for Advanced Research, Nagoya University , Nagoya, Japan
                [4] 4 Center for Research in Isotopes and Environmental Dynamics, University of Tsukuba , Tsukuba, Ibaraki, Japan
                Author notes

                Edited by: Jose M. Mulet, Universitat Politècnica de València, Spain

                Reviewed by: Reyes Rodenas, UMR5546 Laboratoire de Recherche en Sciences Vegetales (LRSV), France; Sho Nishida, Saga University, Japan

                *Correspondence: Nathalie Leonhardt, nathalie.leonhardt@ 123456cea.fr
                Article
                10.3389/fpls.2023.1040118
                10557132
                37810384
                6bec9055-8d90-4722-bb97-ea6063f520b0
                Copyright © 2023 Kanno, Martin, Vallier, Chiarenza, Nobori, Furukawa, Nussaume, Vavasseur and Leonhardt

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 08 September 2022
                : 28 June 2023
                Page count
                Figures: 6, Tables: 2, Equations: 0, References: 58, Pages: 13, Words: 7229
                Funding
                The authors received financial support from the French “Programme Investissement d’Avenir” (ANR 11-RSNR-0005 DEMETERRES, https://anr.fr/ProjetIA-11-RSNR-0005), the French Alternative Energies and Atomic Energy Commission, and JSPS KAKENHI Grant Number 15K18764, and was supported by ERAN I-19-02, F-20-13, F-21-10.
                Categories
                Plant Science
                Original Research
                Custom metadata
                Plant Membrane Traffic and Transport

                Plant science & Botany
                arabidopsis thaliana,hak5,skor,potassium,cesium,transporter
                Plant science & Botany
                arabidopsis thaliana, hak5, skor, potassium, cesium, transporter

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