RIN13 Is a Positive Regulator of the Plant Disease Resistance Protein RPM1
| Autor: | Jong-Hyun Ko, A. Al-Daoude, Marta de Torres Zabala, Murray Grant |
|---|---|
| Rok vydání: | 2005 |
| Předmět: |
Hypersensitive response
Programmed cell death DNA Plant Molecular Sequence Data Arabidopsis Regulator Pseudomonas syringae Virulence Apoptosis Plant Science Plant disease resistance Biology Genes Plant Models Biological Botany Amino Acid Sequence Research Articles Plant Diseases Binding Sites Base Sequence Sequence Homology Amino Acid Arabidopsis Proteins Effector fungi Cell Biology Plants Genetically Modified Recombinant Proteins Cell biology Ectopic expression Gene Deletion |
| Zdroj: | The Plant Cell. 17:1016-1028 |
| ISSN: | 1532-298X |
| DOI: | 10.1105/tpc.104.028720 |
| Popis: | The RPM1 protein confers resistance to Pseudomonas syringae pv tomato DC3000 expressing either of the Type III effector proteins AvrRpm1 or AvrB. Here, we describe the isolation and functional characterization of RPM1 Interacting Protein 13 (RIN13), a resistance protein interactor shown to positively enhance resistance function. Ectopic expression of RIN13 (RIN13s) enhanced bacterial restriction mechanisms but paradoxically abolished the normally rapid hypersensitive response (HR) controlled by RPM1. In contrast with wild-type plants, leaves expressing RIN13s did not undergo electrolyte leakage or accumulate H2O2 after bacterial delivery of AvrRpm1. Overexpression of RIN13 also altered the transcription profile observed during a normal HR. By contrast, RIN13 knockout plants had the same ion leakage signatures and HR timing of wild-type plants in response to DC3000(avrRpm1) but failed to suppress bacterial growth. The modified phenotypes seen in the RIN13s/as plants were specific to recognition of AvrRpm1 or AvrB, and wild-type responses were observed after challenge with other incompatible pathogens or the virulent DC3000 isolate. Our results suggest that cell death is not necessary to confer resistance, and engineering enhanced resistance without activation of programmed cell death is a real possibility. |
| Databáze: | OpenAIRE |
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