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Enhanced Secondary- and Hormone Metabolism in Leaves of Arbuscular MycorrhizalMedicago truncatula

L. Adolfsson, H. Nziengui, IN. Abreu, J. Šimura, A. Beebo, A. Herdean, J. Aboalizadeh, J. Široká, T. Moritz, O. Novák, K. Ljung, B. Schoefs, C. Spetea,

. 2017 ; 175 (1) : 392-411. [pub] 20170711

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc18010424

Arbuscular mycorrhizas (AM) are the most common symbiotic associations between a plant's root compartment and fungi. They provide nutritional benefit (mostly inorganic phosphate [Pi]), leading to improved growth, and nonnutritional benefits, including defense responses to environmental cues throughout the host plant, which, in return, delivers carbohydrates to the symbiont. However, how transcriptional and metabolic changes occurring in leaves of AM plants differ from those induced by Pifertilization is poorly understood. We investigated systemic changes in the leaves of mycorrhizedMedicago truncatulain conditions with no improved Pistatus and compared them with those induced by high-Pitreatment in nonmycorrhized plants. Microarray-based genome-wide profiling indicated up-regulation by mycorrhization of genes involved in flavonoid, terpenoid, jasmonic acid (JA), and abscisic acid (ABA) biosynthesis as well as enhanced expression ofMYC2, the master regulator of JA-dependent responses. Accordingly, total anthocyanins and flavonoids increased, and most flavonoid species were enriched in AM leaves. Both the AM and Pitreatments corepressed iron homeostasis genes, resulting in lower levels of available iron in leaves. In addition, higher levels of cytokinins were found in leaves of AM- and Pi-treated plants, whereas the level of ABA was increased specifically in AM leaves. Foliar treatment of nonmycorrhized plants with either ABA or JA induced the up-regulation ofMYC2, but only JA also induced the up-regulation of flavonoid and terpenoid biosynthetic genes. Based on these results, we propose that mycorrhization and Pifertilization share cytokinin-mediated improved shoot growth, whereas enhanced ABA biosynthesis and JA-regulated flavonoid and terpenoid biosynthesis in leaves are specific to mycorrhization.

Citace poskytuje Crossref.org

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$a Arbuscular mycorrhizas (AM) are the most common symbiotic associations between a plant's root compartment and fungi. They provide nutritional benefit (mostly inorganic phosphate [Pi]), leading to improved growth, and nonnutritional benefits, including defense responses to environmental cues throughout the host plant, which, in return, delivers carbohydrates to the symbiont. However, how transcriptional and metabolic changes occurring in leaves of AM plants differ from those induced by Pifertilization is poorly understood. We investigated systemic changes in the leaves of mycorrhizedMedicago truncatulain conditions with no improved Pistatus and compared them with those induced by high-Pitreatment in nonmycorrhized plants. Microarray-based genome-wide profiling indicated up-regulation by mycorrhization of genes involved in flavonoid, terpenoid, jasmonic acid (JA), and abscisic acid (ABA) biosynthesis as well as enhanced expression ofMYC2, the master regulator of JA-dependent responses. Accordingly, total anthocyanins and flavonoids increased, and most flavonoid species were enriched in AM leaves. Both the AM and Pitreatments corepressed iron homeostasis genes, resulting in lower levels of available iron in leaves. In addition, higher levels of cytokinins were found in leaves of AM- and Pi-treated plants, whereas the level of ABA was increased specifically in AM leaves. Foliar treatment of nonmycorrhized plants with either ABA or JA induced the up-regulation ofMYC2, but only JA also induced the up-regulation of flavonoid and terpenoid biosynthetic genes. Based on these results, we propose that mycorrhization and Pifertilization share cytokinin-mediated improved shoot growth, whereas enhanced ABA biosynthesis and JA-regulated flavonoid and terpenoid biosynthesis in leaves are specific to mycorrhization.
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$a Nziengui, Hugues $u Department of Biological and Environmental Sciences, University of Gothenburg, 405 30 Gothenburg, Sweden.
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$a Šimura, Jan $u Laboratory of Growth Regulators, Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany of Czech Academy of Sciences and Faculty of Science of Palacký University, CZ-78371 Olomouc, Czech Republic.
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$a Beebo, Azeez $u Department of Biological and Environmental Sciences, University of Gothenburg, 405 30 Gothenburg, Sweden.
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$a Herdean, Andrei $u Department of Biological and Environmental Sciences, University of Gothenburg, 405 30 Gothenburg, Sweden.
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$a Moritz, Thomas $u Umeå Plant Science Centre, Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, 901 83 Umea, Sweden.
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$a Novák, Ondřej $u Laboratory of Growth Regulators, Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany of Czech Academy of Sciences and Faculty of Science of Palacký University, CZ-78371 Olomouc, Czech Republic.
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$a Ljung, Karin $u Umeå Plant Science Centre, Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, 901 83 Umea, Sweden.
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$a Schoefs, Benoît $u Metabolism, Engineering of Microalgal Molecules and Applications, Mer Molécules Santé, University Bretagne Loire, Institut Universitaire Mer et Littoral - Fédération de Recherche 3473 Centre National de la Recherche Scientifique, University of Le Mans, 72085 Le Mans cedex 9, France.
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$a Spetea, Cornelia $u Department of Biological and Environmental Sciences, University of Gothenburg, 405 30 Gothenburg, Sweden cornelia.spetea.wiklund@bioenv.gu.se.
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