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dc.contributor.authorArnáiz Alonso, Ana 
dc.contributor.authorTalavera Mateo, Lucía
dc.contributor.authorGonzález Melendi, Pablo
dc.contributor.authorMartínez, Manuel
dc.contributor.authorDiaz, Isabel
dc.contributor.authorSantamaría Fernández, Mª Estrella
dc.date.accessioned2025-01-30T12:22:29Z
dc.date.available2025-01-30T12:22:29Z
dc.date.issued2018
dc.identifier.urihttp://hdl.handle.net/10259/10103
dc.description.abstractTetranychus urticae (two-spotted spider mite) is a striking example of polyphagy among herbivores with an extreme record of pesticide resistance and one of the most significant pests in agriculture. The T. urticae genome contains a large number of cysteine- and serine-proteases indicating their importance in the spider mite physiology. This work is focused on the potential role of the Kunitz trypsin inhibitor (KTI) family on plant defense responses against spider mites. The molecular characterization of two of these genes, AtKTI4 and AtKTI5, combined with feeding bioassays using T-DNA insertion lines for both genes was carried out. Spider mite performance assays showed that independent KTI silencing Arabidopsis lines conferred higher susceptibility to T. urticae than WT plants. Additionally, transient overexpression of these inhibitors in Nicotiana benthamiana demonstrated their ability to inhibit not only serine- but also cysteine-proteases, indicating the bifunctional inhibitory role against both types of enzymes. These inhibitory properties could be involved in the modulation of the proteases that participate in the hydrolysis of dietary proteins in the spider mite gut, as well as in other proteolytic processes.en
dc.description.sponsorshipThis work was supported by projects from Ministerio de Economía y Competitividad of Spain (projects BIO2014-53508-R, 618105-FACCE-Era Net Plus; BIO2017-83472-R).en
dc.format.mimetypeapplication/pdf
dc.language.isoenges
dc.publisherFrontiers Mediaes
dc.relation.ispartofFrontiers in Plant Science. 2018, V. 9, 986es
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectPlant-herbivore interphaseen
dc.subjectTetranychus urticaeen
dc.subjectArabidopsis thalianaen
dc.subjectSerine protease inhibitorsen
dc.subjectCysteine protease inhibitorsen
dc.subjectSpider mite digestionen
dc.subject.otherBiotecnologíaes
dc.subject.otherBiotechnologyen
dc.titleArabidopsis Kunitz Trypsin Inhibitors in Defense Against Spider Mitesen
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.relation.publisherversionhttps://doi.org/10.3389/fpls.2018.00986es
dc.identifier.doi10.3389/fpls.2018.00986
dc.identifier.essn1664-462X
dc.journal.titleFrontiers in Plant Scienceen
dc.volume.number9es
dc.page.initial986es
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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