4.7 Article

TcNPR3 from Theobroma cacao functions as a repressor of the pathogen defense response

期刊

BMC PLANT BIOLOGY
卷 13, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/1471-2229-13-204

关键词

Plant defense; NPR3; Negative regulator; Cacao; NPR1

资金

  1. Pennsylvania State University, College of Agricultural Sciences, The Huck Institutes of Life Sciences
  2. American Research Institute Penn State Endowed Program in the Molecular Biology of Cacao
  3. National Science Foundation BREAD program
  4. Bill and Melinda Gates Foundation [NSF0965353]
  5. Division Of Integrative Organismal Systems
  6. Direct For Biological Sciences [0965353] Funding Source: National Science Foundation

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Background: Arabidopsis thaliana (Arabidopsis) NON-EXPRESSOR OF PR1 (NPR1) is a transcription coactivator that plays a central role in regulating the transcriptional response to plant pathogens. Developing flowers of homozygous npr3 mutants are dramatically more resistant to infection by the pathogenic bacterium Pseudomonas syringae, suggesting a role of NPR3 as a repressor of NPR1-mediated defense response with a novel role in flower development. Results: We report here the characterization of a putative NPR3 gene from the tropical tree species Theobroma cacao (TcNPR3). Like in Arabidopsis, TcNPR3 was constitutively expressed across a wide range of tissue types and developmental stages but with some differences in relative levels compared to Arabidopsis. To test the function of TcNPR3, we performed transgenic complementation analysis by introducing a constitutively expressing putative TcNPR3 transgene into an Arabidopsis npr3 mutant. TcNPR3 expressing Arabidopsis plants were partially restored to the WT pathogen phenotype (immature flowers susceptible to bacterial infection). To test TcNPR3 function directly in cacao tissues, a synthetic microRNA targeting TcNPR3 mRNA was transiently expressed in cacao leaves using an Agrobacterium-infiltration method. TcNPR3 knock down leaf tissues were dramatically more resistance to infection with Phytophthora capsici in a leaf bioassay, showing smaller lesion sizes and reduced pathogen replication. Conclusions: We conclude that TcNPR3 functions similar to the Arabidopsis NPR3 gene in the regulation of the cacao defense response. Since TcNPR3 did not show a perfect complementation of the Arabidopsis NPR3 mutation, the possibility remains that other functions of TcNPR3 remain to be found. This novel knowledge can contribute to the breeding of resistant cacao varieties against pathogens through molecular markers based approaches or biotechnological strategies.

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