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      Reductive stress triggers ANAC017-mediated retrograde signaling to safeguard the endoplasmic reticulum by boosting mitochondrial respiratory capacity

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          Abstract

          Redox processes are at the heart of universal life processes, such as metabolism, signaling, or folding of secreted proteins. Redox landscapes differ between cell compartments and are strictly controlled to tolerate changing conditions and to avoid cell dysfunction. While a sophisticated antioxidant network counteracts oxidative stress, our understanding of reductive stress responses remains fragmentary. Here, we observed root growth impairment in Arabidopsis thaliana mutants of mitochondrial alternative oxidase 1a ( aox1a) in response to the model thiol reductant dithiothreitol (DTT). Mutants of mitochondrial uncoupling protein 1 ( ucp1) displayed a similar phenotype indicating that impaired respiratory flexibility led to hypersensitivity. Endoplasmic reticulum (ER) stress was enhanced in the mitochondrial mutants and limiting ER oxidoreductin capacity in the aox1a background led to synergistic root growth impairment by DTT, indicating that mitochondrial respiration alleviates reductive ER stress. The observations that DTT triggered nicotinamide adenine dinucleotide (NAD) reduction in vivo and that the presence of thiols led to electron transport chain activity in isolated mitochondria offer a biochemical framework of mitochondrion-mediated alleviation of thiol-mediated reductive stress. Ablation of transcription factor Arabidopsis NAC domain-containing protein17 (ANAC017) impaired the induction of AOX1a expression by DTT and led to DTT hypersensitivity, revealing that reductive stress tolerance is achieved by adjusting mitochondrial respiratory capacity via retrograde signaling. Our data reveal an unexpected role for mitochondrial respiratory flexibility and retrograde signaling in reductive stress tolerance involving inter-organelle redox crosstalk.

          Abstract

          Enhancement of mitochondrial respiratory capacity and its control by retrograde signaling aid thiol oxidation and serve reductive ER stress tolerance in Arabidopsis.

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              How mitochondria produce reactive oxygen species

              The production of ROS (reactive oxygen species) by mammalian mitochondria is important because it underlies oxidative damage in many pathologies and contributes to retrograde redox signalling from the organelle to the cytosol and nucleus. Superoxide (O2 •−) is the proximal mitochondrial ROS, and in the present review I outline the principles that govern O2 •− production within the matrix of mammalian mitochondria. The flux of O2 •− is related to the concentration of potential electron donors, the local concentration of O2 and the second-order rate constants for the reactions between them. Two modes of operation by isolated mitochondria result in significant O2 •− production, predominantly from complex I: (i) when the mitochondria are not making ATP and consequently have a high Δp (protonmotive force) and a reduced CoQ (coenzyme Q) pool; and (ii) when there is a high NADH/NAD+ ratio in the mitochondrial matrix. For mitochondria that are actively making ATP, and consequently have a lower Δp and NADH/NAD+ ratio, the extent of O2 •− production is far lower. The generation of O2 •− within the mitochondrial matrix depends critically on Δp, the NADH/NAD+ and CoQH2/CoQ ratios and the local O2 concentration, which are all highly variable and difficult to measure in vivo. Consequently, it is not possible to estimate O2 •− generation by mitochondria in vivo from O2 •−-production rates by isolated mitochondria, and such extrapolations in the literature are misleading. Even so, the description outlined here facilitates the understanding of factors that favour mitochondrial ROS production. There is a clear need to develop better methods to measure mitochondrial O2 •− and H2O2 formation in vivo, as uncertainty about these values hampers studies on the role of mitochondrial ROS in pathological oxidative damage and redox signalling.
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                Author and article information

                Contributors
                Journal
                Plant Cell
                Plant Cell
                plcell
                The Plant Cell
                Oxford University Press
                1040-4651
                1532-298X
                April 2022
                25 January 2022
                25 January 2022
                : 34
                : 4
                : 1375-1395
                Affiliations
                Institute of Plant Biology and Biotechnology (IBBP), Westfälische Wilhelms-Universität Münster , D-48143 Münster, Germany
                Institute of Crop Science and Resource Conservation (INRES), Rheinische Friedrich-Wilhelms-Universität Bonn , D-53113 Bonn, Germany
                Institute of Crop Science and Resource Conservation (INRES), Rheinische Friedrich-Wilhelms-Universität Bonn , D-53113 Bonn, Germany
                Institute of Plant Biology and Biotechnology (IBBP), Westfälische Wilhelms-Universität Münster , D-48143 Münster, Germany
                Institute of Crop Science and Resource Conservation (INRES), Rheinische Friedrich-Wilhelms-Universität Bonn , D-53113 Bonn, Germany
                Institute of Plant Biology and Biotechnology (IBBP), Westfälische Wilhelms-Universität Münster , D-48143 Münster, Germany
                Institute of Crop Science and Resource Conservation (INRES), Rheinische Friedrich-Wilhelms-Universität Bonn , D-53113 Bonn, Germany
                Institute of Plant Biology and Biotechnology (IBBP), Westfälische Wilhelms-Universität Münster , D-48143 Münster, Germany
                Institute of Plant Biology and Biotechnology (IBBP), Westfälische Wilhelms-Universität Münster , D-48143 Münster, Germany
                Institute of Crop Science and Resource Conservation (INRES), Rheinische Friedrich-Wilhelms-Universität Bonn , D-53113 Bonn, Germany
                Institute of Crop Science and Resource Conservation (INRES), Rheinische Friedrich-Wilhelms-Universität Bonn , D-53113 Bonn, Germany
                Institute of Crop Science and Resource Conservation (INRES), Rheinische Friedrich-Wilhelms-Universität Bonn , D-53113 Bonn, Germany
                Institute of Plant Biology and Biotechnology (IBBP), Westfälische Wilhelms-Universität Münster , D-48143 Münster, Germany
                Institute of Crop Science and Resource Conservation (INRES), Rheinische Friedrich-Wilhelms-Universität Bonn , D-53113 Bonn, Germany
                Author notes

                These authors contributed equally (F.B., S.L., and J.M.U.)

                [†]

                Present address: Andermatt Biocontrol AG, CH-6146 Grossdietwil, Switzerland

                [‡]

                Present address: Institute of Physiology I, Medical Faculty, University of Bonn, D-53115 Bonn, Germany

                [§]

                Present address: Department of Biosciences, University of Milan, I-20133 Milan, Italy

                [¶]

                Present address: Max-Planck-Institute for Plant Breeding Research, D-50829 Cologne, Germany

                [ ∥ ]

                Present address: Department of Biology, TU Kaiserslautern, D-67663 Kaiserslautern, Germany

                [††]

                Senior author

                Author information
                https://orcid.org/0000-0001-6379-853X
                https://orcid.org/0000-0001-8343-1399
                https://orcid.org/0000-0003-4525-6555
                https://orcid.org/0000-0002-0601-4302
                https://orcid.org/0000-0002-2523-2372
                https://orcid.org/0000-0003-4647-6365
                https://orcid.org/0000-0002-9013-1412
                https://orcid.org/0000-0001-5369-7911
                https://orcid.org/0000-0003-4061-1175
                https://orcid.org/0000-0001-8144-4364
                https://orcid.org/0000-0003-0796-8308
                Article
                koac017
                10.1093/plcell/koac017
                9125394
                35078237
                ebdbdb1f-2596-4bdc-9d88-d9d9c35f5b72
                © The Author(s) 2022. Published by Oxford University Press on behalf of American Society of Plant Biologists.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 13 May 2021
                : 18 December 2021
                : 08 February 2022
                Page count
                Pages: 21
                Funding
                Funded by: Deutsche Forschungsgemeinschaft through the Research Training Group GRK 2064 “Water use efficiency and drought stress responses: From Arabidopsis to Barley;
                Funded by: Dynamics of thiol-based redox switches in cellular physiology;
                Award ID: ME1567/9-2
                Award ID: SCHW1719/7-1
                Funded by: INST211/903-1 FUGG and the project;
                Award ID: SCHW1719/5-1
                Categories
                Research Articles
                AcademicSubjects/SCI02286
                AcademicSubjects/SCI02287
                AcademicSubjects/SCI01270
                AcademicSubjects/SCI01280
                AcademicSubjects/SCI02288

                Plant science & Botany
                Plant science & Botany

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