Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/122649
Title: Dissecting gene metabolite relationships in the Medicago truncatula terpenome after Aphanomyces euteiches infection
Author(s): Harding, Esther ArmahLook up in the Integrated Authority File of the German National Library
Referee(s): Hause, BettinaLook up in the Integrated Authority File of the German National Library
Tholl, Dorothea
Tissier, AlainLook up in the Integrated Authority File of the German National Library
Granting Institution: Martin-Luther-Universität Halle-Wittenberg
Issue Date: 2025
Extent: 1 Online-Ressource (ix, 136 Seiten)
Type: HochschulschriftLook up in the Integrated Authority File of the German National Library
Type: PhDThesis
Exam Date: 2025-12-02
Language: English
URN: urn:nbn:de:gbv:3:4-1981185920-1245940
Abstract: Sesquiterpenes produced by terpene synthases (TPS) play key roles in plant defense. In Medicago truncatula, MtTPS10 was previously the only TPS linked to resistance against the root pathogen Aphanomyces euteiches, and its induction appears to be triggered by an A. euteiches elicitor (elicitor M) acting as a PAMP. Transcriptomic and metabolomic analyses revealed M. truncatula ecotype-specific defense strategies: Jemalong A17 expresses MtTPS10, while ecotype 368 expresses MITPS25 following pathogen contact. MtTPS25 encodes a root-specific sesquiterpene synthase that produces α-copaene as the main volatile, a role confirmed by RNAi silencing. Engineering potato plants with MtTPS enhanced resistance to Phytophthora infestans. Additionally, the cytochrome P450 CYP71D62 was identified as a candidate gene modifying the MtTPS10 sesquiterpene product, himachalol in planta. Together, these findings highlight the importance of terpene-mediated defenses in legumes and their potential for crop protection.
URI: https://opendata.uni-halle.de//handle/1981185920/124594
http://dx.doi.org/10.25673/122649
Open Access: Open access publication
License: (CC BY 4.0) Creative Commons Attribution 4.0(CC BY 4.0) Creative Commons Attribution 4.0
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