In situ localization of PR-1 mRNA and PR-1 protein in compatible and incompatible interactions of pepper stems withPhytophthora capsici |
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Authors: | Yeon Kyeong Lee S. Hippe-Sanwald Sung Chul Lee H. Hohenberg Byung Kook Hwang |
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Affiliation: | (1) Department of Agricultural Biology, Korea University, 136–701 Anam-dong, Sungbuk-ku, Seoul, Korea;(2) Institute of Phytopathology, University of Kiel, Kiel;(3) Heinrich-Pette-Institute, University of Hamburg, Hamburg |
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Abstract: | Summary In situ hybridization and immunogold labeling were performed to examine the temporal and spatial expression pattern of pathogenesis-related protein 1 (CABPR1) mRNA and PR-1 protein in pepper (Capsicum annuum L.) stem tissues infected by virulent and avirulent isolates ofPhytophthora capsici. CABPR1 mRNA accumulation was confirmed in the infected pepper stem tissue by Northern blot analysis and in situ hybridization. Northern blot analysis showed that the temporal expression ofCABPR1 mRNA varied greatly between compatible and incompatible interactions. An earlier expression of theCABPR1 gene, 6 h after inoculation, was observed in the incompatible interaction. In situ hybridization results revealed thatCABPR1 mRNA was expressed in the phloem areas of vascular bundles in infected pepper stem tissues, but especially strongly in the incompatible interaction. PR-1 protein was predominantly found in the intercellular spaces of pepper stem cells in the compatible and incompatible interactions 24 h after inoculation. Strikingly, the immunogold labeling was associated with fibrillar and electron-dense material localized in the intercellular space. Dense labeling of PR-1 protein was also seen at the interface of the pathogen and the host cell wall, whereas few gold particles were detected over the host cytoplasm. However, PR-1 protein was not detected over the fungal cell wall in either interaction. |
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Keywords: | Pathogenesis-related protein 1 CABPR1 gene In situ hybridization Immunogold labeling Capsicum annuum Phytophthora capsici |
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