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The function of S-nitrosothiols during abiotic stress in plants

dc.contributor.authorBegara-Morales, J.C.
dc.contributor.authorChaki, M.
dc.contributor.authorValderrama, R.
dc.contributor.authorMata-Pérez, C.
dc.contributor.authorPadilla, M. N.
dc.contributor.authorBarroso, J. B.
dc.date.accessioned2025-01-07T07:18:30Z
dc.date.available2025-01-07T07:18:30Z
dc.date.issued2019-04-27
dc.description.abstractNitric oxide (NO) is an active redox molecule involved in the control of a wide range of functions integral to plant biology. For instance, NO is implicated in seed germination, floral development, senescence, stomatal closure, and plant responses to stress. NO usually mediates signaling events via interactions with different biomolecules, for example the modulation of protein functioning through post-translational modifications (NO-PTMs). S-nitrosation is a reversible redox NO-PTM that consists of the addition of NO to a specific thiol group of a cysteine residue, leading to formation of S-nitrosothiols (SNOs). SNOs are more stable than NO and therefore they can extend and spread the in vivo NO signaling. The development of robust and reliable detection methods has allowed the identification of hundreds of S-nitrosated proteins involved in a wide range of physiological and stress-related processes in plants. For example, SNOs have a physiological function in plant development, hormone metabolism, nutrient uptake, and photosynthesis, among many other processes. The role of S-nitrosation as a regulator of plant responses to salinity and drought stress through the modulation of specific protein targets has also been well established. However, there are many S-nitrosated proteins that have been identified under different abiotic stresses for which the specific roles have not yet been identified. In this review, we examine current knowledge of the specific role of SNOs in the signaling events that lead to plant responses to abiotic stress, with a particular focus on examples where their functions have been well characterized at the molecular level.es_ES
dc.description.sponsorshipJCBM wishes to thank the Ministry of Economy and Competitiveness (Spain) for postdoctoral research funding within the Juan de la Cierva- Incorporación program (IJCI-2015–23438). The work in our lab is supported by ERDF grants co-financed by the Ministry of Economy and Competitiveness (project PGC2018-096405-B-I00) and the Junta de Andalucía (group BIO286) in Spain.es_ES
dc.identifier.citationJournal of Experimental Botany, Vol. 70, No. 17 pp. 4429–4439, 2019es_ES
dc.identifier.issn0022-0957es_ES
dc.identifier.otherdoi:10.1093/jxb/erz197es_ES
dc.identifier.urihttps://hdl.handle.net/10953/3714
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.relation.ispartofJournal of Experimental Botanyes_ES
dc.rightsAtribución-SinDerivadas 3.0 España*
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nd/3.0/es/*
dc.subjectAbiotic stresses_ES
dc.subjectantioxidantes_ES
dc.subjectnitric oxidees_ES
dc.subjectS-nitrosothiolses_ES
dc.subjectS-nitrosylationes_ES
dc.subjectsignalinges_ES
dc.titleThe function of S-nitrosothiols during abiotic stress in plantses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.type.versioninfo:eu-repo/semantics/acceptedVersiones_ES

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