The RhWRKY33a-RhPLATZ9 regulatory module delays petal senescence by suppressing rapid reactive oxygen species accumulation in rose flowers.
Li-Wei JiangKun LiuTao ZhangJin ChenSiqi ZhaoYusen CuiWentong ZhouYi YuSiyu ChenCaiyuan WangChangqing ZhangPublished in: The Plant journal : for cell and molecular biology (2023)
Redox homeostasis in plant cells is critical for maintaining normal growth and development, as reactive oxygen species (ROS) can function as signaling molecules or toxic compounds. However, how plants fine-tune redox homeostasis during natural or stress-induced senescence remains unclear. Cut roses (Rosa hybrida), an economically important ornamental product worldwide, often undergo stress-induced precocious senescence at the postharvest bud stage. Here we identified RhPLATZ9, an age- and dehydration-induced PLATZ (plant AT-rich sequence and zinc-binding) protein and determined that it functions as a transcriptional repressor in rose flowers during senescence. We also showed that RhWRKY33a regulates RhPLATZ9 expression during flower senescence. RhPLATZ9-silenced flowers and RhWRKY33a-silenced flowers showed accelerated senescence, with higher ROS contents than the control. By contrast, overexpression of RhWRKY33a or RhPLATZ9 delayed flower senescence, and overexpression in rose calli showed lower ROS accumulation than the control. RNA-seq analysis revealed that apoplastic NADPH oxidase genes (RhRbohs) were enriched among the upregulated differentially expressed genes in RhPLATZ9-silenced flowers compared to wild-type flowers. Yeast one-hybrid assays, electrophoretic mobility shift assays, dual luciferase assays, and chromatin immunoprecipitation quantitative PCR confirmed that the RhRbohD gene is a direct target of RhPLATZ9. These findings suggest that the RhWRKY33a-RhPLATZ9-RhRbohD regulatory module acts as a brake to help maintain ROS homeostasis in petals and thus antagonize age- and stress-induced precocious senescence in rose flowers.
Keyphrases
- stress induced
- reactive oxygen species
- dna damage
- transcription factor
- rna seq
- genome wide
- cell death
- binding protein
- single cell
- gene expression
- high throughput
- induced apoptosis
- cell proliferation
- genome wide identification
- oxidative stress
- air pollution
- magnetic resonance imaging
- high glucose
- contrast enhanced
- endoplasmic reticulum stress
- drug induced
- sensitive detection