Brassinosteroids (BRs) are essential steroid hormones that coordinate plant growth, development and adaptation to changing environments. Although BR signaling has long been viewed primarily as a phosphorylation-dependent pathway, increasing evidence shows that ubiquitination provides an additional regulatory layer that shapes the abundance, activity, subcellular distribution and turnover of key signaling components. Ubiquitin-mediated regulation operates at multiple points in the BR pathway, including receptor homeostasis at the plasma membrane, turnover of GSK3-like kinases, and stability control of the transcription factors BES1/BZR1. These processes determine not only the strength and duration of BR signaling but also its coordination with other hormonal and stress-response pathways. In this review, we discuss recent advances in ubiquitin-mediated regulation of BR signaling, focusing on receptor-level control, proteolytic regulation of core signaling components, and modulation of transcriptional outputs. We also highlight emerging links between ubiquitination, selective autophagy, deubiquitination and BR-associated stress responses and outline key questions concerning ubiquitin chain specificity, substrate recognition and conservation of these regulatory modules in crops. Defining how ubiquitination fine-tunes BR signaling will deepen our understanding of plant steroid hormone regulation and may provide new strategies for optimizing crop architecture, productivity, and stress resilience.

Brassinosteroids (BRs) are essential steroid hormones that coordinate plant growth, development and adaptation to changing environments. Although BR signaling has long been viewed primarily as a phosphorylation-dependent pathway, increasing evidence shows that ubiquitination provides an additional regulatory layer that shapes the abundance, activity, subcellular distribution and turnover of key signaling components. Ubiquitin-mediated regulation operates at multiple points in the BR pathway, including receptor homeostasis at the plasma membrane, turnover of GSK3-like kinases, and stability control of the transcription factors BES1/BZR1. These processes determine not only the strength and duration of BR signaling but also its coordination with other hormonal and stress-response pathways. In this review, we discuss recent advances in ubiquitin-mediated regulation of BR signaling, focusing on receptor-level control, proteolytic regulation of core signaling components, and modulation of transcriptional outputs. We also highlight emerging links between ubiquitination, selective autophagy, deubiquitination and BR-associated stress responses, and outline key questions concerning ubiquitin chain specificity, substrate recognition and conservation of these regulatory modules in crops. Defining how ubiquitination fine-tunes BR signaling will deepen our understanding of plant steroid hormone regulation and may provide new strategies for optimizing crop architecture, productivity and stress resilience.

The brown planthopper (BPH, Nilaparvata lugens) is a major insect pest of rice (Oryza sativa L.) causing severe yield losses across Asia. Although the resistance gene OsBph32 from the cultivar Ptb33 enhances BPH resistance, its molecular and physiological mechanisms remain unclear. Here, we investigated its function using OsBph32-overexpressing lines combined with physiological, transcriptomic, and metabolomic analyses. Overexpression of OsBph32 in the susceptible cultivar 9311 significantly increased resistance to BPH, as indicated by reduced plant damage and suppressed insect growth. This was associated with increased reactive oxygen species accumulation and callose deposition, suggesting activation of early defense responses. Multi-omics analyses revealed that OsBph32 is associated with transcriptional changes in genes involved in cell wall biosynthesis, phenylpropanoid metabolism, and carbon metabolism. Metabolomic profiling further showed increased accumulation of flavonoids, phenolamides, and lignin-related metabolites under BPH infestation, together with changes in carbon metabolism and starch accumulation. Collectively, these results suggest that OsBph32 is associated with coordinated changes in structural reinforcement, secondary metabolism, and carbon metabolism during insect attack, which may contribute to enhanced rice resistance and provide new insights into non-NLR-mediated insect defense mechanisms in plants.