MYB16 and MYB106 promote conical cell morphogenesis by modulating cuticle production, apoplastic pH , and microtubule organization
Abstract
R2R3 MYB transcription factors, such as MYB16 and MYB106 (MYB16/106) in Arabidopsis thaliana, are recognized for their role in conical cell specification. However, the mechanism by which MYB16/106 orchestrate the morphogenesis of conical cells remains poorly understood. Here, we combined genetic analysis, transcriptomics, metabolomics, and live-cell imaging to clarify the MYB16/106-mediated conical cell development in Arabidopsis. Genetic characterization revealed that the myb16 myb106 double mutant exhibited flattened adaxial petal epidermal cells, having lost the wild-type conical shape, and displayed significantly disrupted cuticle nanoridge formation. Transcriptomic (RNA-seq) and chromatin immunoprecipitation-quantitative PCR (ChIP-qPCR) analyses identified the direct transcriptional targets of MYB16/106, which include CYP86A7, CUS2, RXF26, and ABCB13. These genes encode pivotal regulators of cuticular wax and cutin biosynthesis, as well as lipid transport. Metabolomic profiling further validated that MYB16/106 coordinately modulate metabolic pathways associated with cuticle formation, consistent with their transcriptional regulation of cuticle-related targets. Furthermore, the myb16 and myb106 mutants exhibited physiological and cytoskeletal alterations, including an elevated apoplastic pH and disrupted cortical microtubule (CMT) organization. Collectively, our findings establish a hierarchical regulatory framework in which MYB16/106 act as central coordinators, integrating three cellular processes - cuticle biosynthesis, apoplastic pH balance, and CMT organization - to regulate conical cell morphogenesis.
Fields of Study & Subjects
Plant Surface Properties and Treatments
Polysaccharides and Plant Cell Walls
Lipid metabolism and biosynthesis
Publication details
- Journal / source
- New Phytologist
- Publisher
- Wiley
- Volume
- 250
- Issue
- 2
- Pages
- 1092–1110
- Publication date
- 30 January 2026
- Language
- EN