Re‐targeting of a plant defense protease by a cyst nematode effector

dc.contributor.author Pogorelko, Gennady
dc.contributor.author Juvale, Parijat
dc.contributor.author Rutter, William
dc.contributor.author Hütten, Marion
dc.contributor.author Maier, Thomas
dc.contributor.author Hewezi, Tarek
dc.contributor.author Paulus, Judith
dc.contributor.author van der Hoorn, Renier
dc.contributor.author Grundler, Florian
dc.contributor.author Siddique, Shahid
dc.contributor.author Lionetti, Vincenzo
dc.contributor.author Zabotina, Olga
dc.contributor.author Baum, Thomas
dc.contributor.department Plant Pathology and Microbiology
dc.contributor.department Biochemistry, Biophysics and Molecular Biology, Roy J. Carver Department of
dc.date 2019-10-18T15:42:50.000
dc.date.accessioned 2020-06-30T06:23:27Z
dc.date.available 2020-06-30T06:23:27Z
dc.date.issued 2019-06-01
dc.description.abstract <p>Plants mount defense responses during pathogen attacks, and robust host defense suppression by pathogen effector proteins is essential for infection success. 4E02 is an effector of the sugar beet cyst nematode <em>Heterodera schachtii</em>. <em>Arabidopsis thaliana</em> lines expressing the effector‐coding sequence showed altered expression levels of defense response genes, as well as higher susceptibility to both the biotroph <em>H. schachtii</em> and the necrotroph <em>Botrytis cinerea</em>, indicating a potential suppression of defenses by 4E02. Yeast two‐hybrid analyses showed that 4E02 targets <em>A. thaliana</em> vacuolar papain‐like cysteine protease (PLCP) ‘Responsive to Dehydration 21A’ (RD21A)<em>,</em> which has been shown to function in the plant defense response. Activity‐based protein profiling analyses documented that the <em>in planta</em> presence of 4E02 does not impede enzymatic activity of RD21A. Instead, 4E02 mediates a re‐localization of this protease from the vacuole to the nucleus and cytoplasm, which is likely to prevent the protease from performing its defense function and at the same time, brings it in contact with novel substrates. Yeast two‐hybrid analyses showed that RD21A interacts with multiple host proteins including enzymes involved in defense responses as well as carbohydrate metabolism. In support of a role in carbohydrate metabolism of RD21A after its effector‐mediated re‐localization, we observed cell wall compositional changes in 4E02 expressing <em>A. thaliana</em> lines. Collectively, our study shows that 4E02 removes RD21A from its defense‐inducing pathway and repurposes this enzyme by targeting the active protease to different cell compartments.</p>
dc.description.comments <p>This article is published as Pogorelko, Gennady V., Parijat S. Juvale, William B. Rutter, Marion Hütten, Thomas R. Maier, Tarek Hewezi, Judith Paulus et al. "Re‐targeting of a plant defense protease by a cyst nematode effector." <em>The Plant Journal</em> 98 (2019): 1000-1014. doi: <a href="https://doi.org/10.1111/tpj.14295">10.1111/tpj.14295</a>.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/plantpath_pubs/279/
dc.identifier.articleid 1269
dc.identifier.contextkey 15563261
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath plantpath_pubs/279
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/57731
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/plantpath_pubs/279/2019_Baum_RetargetingPlant.pdf|||Fri Jan 14 23:08:16 UTC 2022
dc.source.uri 10.1111/tpj.14295
dc.subject.disciplines Agricultural Science
dc.subject.disciplines Biochemistry, Biophysics, and Structural Biology
dc.subject.disciplines Entomology
dc.subject.disciplines Molecular Genetics
dc.subject.disciplines Plant Pathology
dc.subject.keywords effector
dc.subject.keywords nematode
dc.subject.keywords plant–pathogen interaction
dc.subject.keywords protease
dc.subject.keywords re-localization
dc.subject.keywords defense
dc.title Re‐targeting of a plant defense protease by a cyst nematode effector
dc.type article
dc.type.genre article
dspace.entity.type Publication
relation.isAuthorOfPublication ea8d53ba-1a8f-4f5c-9b4a-1ecbd67e2f43
relation.isOrgUnitOfPublication a26b5928-54bb-4a0b-a973-95d649d1ad83
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