<p>The <i>Arabidopsis seor1ko</i> line, which expresses the protein AtSEOR2 free of its bond with AtSEOR1, exhibits a lower phytoplasma titre as compared to wild type plants. In search for mechanism(s) underlying potential SEOR2-mediated defense responses the transcriptome of healthy wild type and <i>Atseor1ko</i> plants was disclosed by RNA sequencing. Comparative transcriptome analysis revealed 1036 differentially expressed genes (DEGs, 893 up- and 143 down-regulated) between the <i>Atseor1ko</i> line and the wild type. Sequence annotation and classification of the up-regulated genes identified “plant-pathogen interaction” among the most enriched clusters. The “plant-pathogen interaction” cluster included genes encoding members of the protein kinase superfamily, actors in calcium/calmodulin signaling transduction and WRKY transcription factors. An interaction network analysis and a host-phytoplasma interaction map demonstrated that AtSEOR2 protein could interact with the calcium-binding proteins CAM2 and TCH3. The latter one also turned out to be an indirect target of the SAP54<sub>CY</sub> phytoplasma effector, which suggests a SEOR2-mediated role of TCH3 in balancing nutrient investments in plant defense and plant growth.</p>

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SEOR2 in Arabidopsis mediates Ca2+ dependent defense against phytoplasmas and reduction of plant growth

  • Keziah Omenge,
  • Ottone Carmelo Viscardo,
  • Fernando Rodrigo De Oliveira Cantao,
  • Simonetta Santi,
  • Aart Jan Eeuwe van Bel,
  • Rita Musetti

摘要

The Arabidopsis seor1ko line, which expresses the protein AtSEOR2 free of its bond with AtSEOR1, exhibits a lower phytoplasma titre as compared to wild type plants. In search for mechanism(s) underlying potential SEOR2-mediated defense responses the transcriptome of healthy wild type and Atseor1ko plants was disclosed by RNA sequencing. Comparative transcriptome analysis revealed 1036 differentially expressed genes (DEGs, 893 up- and 143 down-regulated) between the Atseor1ko line and the wild type. Sequence annotation and classification of the up-regulated genes identified “plant-pathogen interaction” among the most enriched clusters. The “plant-pathogen interaction” cluster included genes encoding members of the protein kinase superfamily, actors in calcium/calmodulin signaling transduction and WRKY transcription factors. An interaction network analysis and a host-phytoplasma interaction map demonstrated that AtSEOR2 protein could interact with the calcium-binding proteins CAM2 and TCH3. The latter one also turned out to be an indirect target of the SAP54CY phytoplasma effector, which suggests a SEOR2-mediated role of TCH3 in balancing nutrient investments in plant defense and plant growth.