Differential Roles of Two Homologous Cyclin-Dependent Kinase Inhibitor Genes in Regulating Cell Cycle and Innate Immunity in Arabidopsis.
Safae HamdounChong ZhangManroop GillNarender KumarMichelle ChurchmanJohn C LarkinAshley KwonHua LuPublished in: Plant physiology (2015)
Precise cell-cycle control is critical for plant development and responses to pathogen invasion. Two homologous cyclin-dependent kinase inhibitor genes, SIAMESE (SIM) and SIM-RELATED 1 (SMR1), were recently shown to regulate Arabidopsis (Arabidopsis thaliana) defense based on phenotypes conferred by a sim smr1 double mutant. However, whether these two genes play differential roles in cell-cycle and defense control is unknown. In this report, we show that while acting synergistically to promote endoreplication, SIM and SMR1 play different roles in affecting the ploidy of trichome and leaf cells, respectively. In addition, we found that the smr1-1 mutant, but not sim-1, was more susceptible to a virulent Pseudomonas syringae strain, and this susceptibility could be rescued by activating salicylic acid (SA)-mediated defense. Consistent with these results, smr1-1 partially suppressed the dwarfism, high SA levels, and cell death phenotypes in acd6-1, a mutant used to gauge the change of defense levels. Thus, SMR1 functions partly through SA in defense control. The differential roles of SIM and SMR1 are due to differences in temporal and spatial expression of these two genes in Arabidopsis tissues and in response to P. syringae infection. In addition, flow-cytometry analysis of plants with altered SA signaling revealed that SA is necessary, but not sufficient, to change cell-cycle progression. We further found that a mutant with three CYCD3 genes disrupted also compromised disease resistance to P. syringae. Together, this study reveals differential roles of two homologous cyclin-dependent kinase inhibitors in regulating cell-cycle progression and innate immunity in Arabidopsis and provides insights into the importance of cell-cycle control during host-pathogen interactions.
Keyphrases
- cell cycle
- cell proliferation
- transcription factor
- genome wide
- genome wide identification
- cell death
- bioinformatics analysis
- flow cytometry
- arabidopsis thaliana
- dna damage
- innate immune
- plant growth
- wild type
- cell cycle arrest
- cell wall
- poor prognosis
- genome wide analysis
- gene expression
- dna methylation
- signaling pathway
- candida albicans
- induced apoptosis
- single cell
- staphylococcus aureus
- long non coding rna
- binding protein
- cell migration
- escherichia coli
- endoplasmic reticulum stress
- drug induced