CaSBP11 Participates in the Defense Response of Pepper to Phytophthora capsici through Regulating the Expression of Defense-Related Genes

Int J Mol Sci. 2020 Nov 28;21(23):9065. doi: 10.3390/ijms21239065.

Abstract

Squamosa promoter binding protein (SBP)-box genes are plant-specific transcription factors involved in plant growth and development, morphogenesis and biotic and abiotic stress responses. However, these genes have been understudied in pepper, especially with respect to defense responses to Phytophthora capsici infection. CaSBP11 is a SBP-box family gene in pepper that was identified in our previous research. Silencing CaSBP11 enhanced the defense response of pepper plants to Phytophthora capsici. Without treatment, the expression of defense-related genes (CaBPR1, CaPO1, CaSAR8.2 and CaDEF1) increased in CaSBP11-silenced plants. However, the expression levels of these genes were inhibited under transient CaSBP11 expression. CaSBP11 overexpression in transgenic Nicotiana benthamiana decreased defense responses, while in Arabidopsis, it induced or inhibited the expression of genes in the salicylic acid and jasmonic acid signaling pathways. CaSBP11 overexpression in sid2-2 mutants induced AtNPR1, AtNPR3, AtNPR4, AtPAD4, AtEDS1, AtEDS5, AtMPK4 and AtNDR1 expression, while AtSARD1 and AtTGA6 expression was inhibited. CaSBP11 overexpression in coi1-21 and coi1-22 mutants, respectively, inhibited AtPDF1.2 expression and induced AtPR1 expression. These results indicate CaSBP11 has a negative regulatory effect on defense responses to Phytophthora capsici. Moreover, it may participate in the defense response of pepper to Phytophthora capsici by regulating defense-related genes and the salicylic and jasmonic acid-mediated disease resistance signaling pathways.

Keywords: CaSBP11; Nicotiana benthamiana; Phytophthora capsici; defense-related genes; pepper.

MeSH terms

  • Arabidopsis / genetics
  • Capsicum / genetics
  • Capsicum / immunology*
  • Cell Nucleus / metabolism
  • Cyclopentanes / metabolism
  • Disease Resistance / genetics
  • Gene Expression Regulation, Plant*
  • Gene Silencing
  • Models, Biological
  • Mutation / genetics
  • Nicotiana / genetics
  • Nicotiana / microbiology
  • Oxylipins / metabolism
  • Phenotype
  • Phytophthora / physiology*
  • Plant Diseases / genetics*
  • Plant Diseases / immunology*
  • Plant Diseases / microbiology
  • Plant Proteins / metabolism*
  • Plants, Genetically Modified
  • Protein Transport
  • Signal Transduction

Substances

  • Cyclopentanes
  • Oxylipins
  • Plant Proteins
  • jasmonic acid