A mitochondria-targeted coenzyme Q peptoid induces superoxide dismutase and alleviates salinity stress in plant cells.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
14 07 2020
Historique:
received: 13 11 2019
accepted: 10 06 2020
entrez: 16 7 2020
pubmed: 16 7 2020
medline: 15 12 2020
Statut: epublish

Résumé

Salinity is a serious challenge to global agriculture and threatens human food security. Plant cells can respond to salt stress either by activation of adaptive responses, or by programmed cell death. The mechanisms deciding the respective response are far from understood, but seem to depend on the degree, to which mitochondria can maintain oxidative homeostasis. Using plant PeptoQ, a Trojan Peptoid, as vehicle, it is possible to transport a coenzyme Q10 (CoQ10) derivative into plant mitochondria. We show that salinity stress in tobacco BY-2 cells (Nicotiana tabacum L. cv Bright Yellow-2) can be mitigated by pretreatment with plant PeptoQ with respect to numerous aspects including proliferation, expansion, redox homeostasis, and programmed cell death. We tested the salinity response for transcripts from nine salt-stress related-genes representing different adaptive responses. While most did not show any significant response, the salt response of the transcription factor NtNAC, probably involved in mitochondrial retrograde signaling, was significantly modulated by the plant PeptoQ. Most strikingly, transcripts for the mitochondrial, Mn-dependent Superoxide Dismutase were rapidly and drastically upregulated in presence of the peptoid, and this response was disappearing in presence of salt. The same pattern, albeit at lower amplitude, was seen for the sodium exporter SOS1. The findings are discussed by a model, where plant PeptoQ modulates retrograde signalling to the nucleus leading to a strong expression of mitochondrial SOD, what renders mitochondria more resilient to perturbations of oxidative balance, such that cells escape salt induced cell death and remain viable.

Identifiants

pubmed: 32665569
doi: 10.1038/s41598-020-68491-4
pii: 10.1038/s41598-020-68491-4
pmc: PMC7360622
doi:

Substances chimiques

Peptoids 0
Reactive Oxygen Species 0
Ubiquinone 1339-63-5
Superoxide Dismutase EC 1.15.1.1
coenzyme Q10 EJ27X76M46

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

11563

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Auteurs

Kinfemichael Geressu Asfaw (KG)

Molecular Cell Biology, Botanical Institute, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, D-76131, Karlsruhe, Germany. kinfe_michael2006@yahoo.com.

Qiong Liu (Q)

Molecular Cell Biology, Botanical Institute, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, D-76131, Karlsruhe, Germany.

Xiaolu Xu (X)

Molecular Cell Biology, Botanical Institute, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, D-76131, Karlsruhe, Germany.

Christina Manz (C)

Molecular Cell Biology, Botanical Institute, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, D-76131, Karlsruhe, Germany.

Sabine Purper (S)

Molecular Cell Biology, Botanical Institute, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, D-76131, Karlsruhe, Germany.

Rose Eghbalian (R)

Molecular Cell Biology, Botanical Institute, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, D-76131, Karlsruhe, Germany.

Stephan W Münch (SW)

Institute of Organic Chemistry, Organic Chemistry I, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, D-76131, Karlsruhe, Germany.
Institute of Biological and Chemical Systems-Functional Molecular Systems (IBCS-FMS), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, D-76344, Eggenstein-Leopoldshafen, Germany.

Ilona Wehl (I)

Institute of Organic Chemistry, Organic Chemistry I, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, D-76131, Karlsruhe, Germany.
Institute of Biological and Chemical Systems-Functional Molecular Systems (IBCS-FMS), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, D-76344, Eggenstein-Leopoldshafen, Germany.

Stefan Bräse (S)

Institute of Organic Chemistry, Organic Chemistry I, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, D-76131, Karlsruhe, Germany.
Institute of Biological and Chemical Systems-Functional Molecular Systems (IBCS-FMS), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, D-76344, Eggenstein-Leopoldshafen, Germany.

Elisabeth Eiche (E)

Institute of Applied Geochemistry (AGW), Geochemistry and Economic Geology Group, Karlsruhe Institute of Technology (KIT), Adenauerring 20b, D-76131, Karlsruhe, Germany.

Bettina Hause (B)

Department of Cell and Metabolic Biology, Leibniz Institute of Plant Biochemistry, Weinberg 3, D-06120, Halle (Saale), Germany.

Ivan Bogeski (I)

Molecular Physiology, Institute of Cardiovascular Physiology, University Medical Center, Georg-August-University, 37073, Göttingen, Germany.

Ute Schepers (U)

Institute of Organic Chemistry, Organic Chemistry I, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, D-76131, Karlsruhe, Germany.
Institute of Functional Interfaces (IFG), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, D-76344, Eggenstein-Leopoldshafen, Germany.

Michael Riemann (M)

Molecular Cell Biology, Botanical Institute, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, D-76131, Karlsruhe, Germany.

Peter Nick (P)

Molecular Cell Biology, Botanical Institute, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, D-76131, Karlsruhe, Germany.

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