We identified the monogenic recessive maize (Zea mays L.) mutant dizzy1 in a segregating F2-family by a forward genetic screen of the BonnMu population, a sequence-indexed collection of Mutator transposon-induced mutants. dizzy1 exhibits a dwarf phenotype with pronounced twisting of leaves and roots. Histological analyses revealed irregular cell organization in dizzy1, including enlarged upper epidermal cells in leaves and disorganized cortical cell architecture in roots. Physiological analysis of primary roots indicated reduced cell viability, reflected by increased membrane permeability and altered metabolic activity. Hormone response assays further showed that dizzy1 is insensitive to brassinolide, exhibits a delayed auxin-promoted shoot response, and displays altered gibberellin effects on lateral root development. Bulked segregant RNA sequencing mapped the dizzy1 locus to chromosome 2. Comparative transcriptome profiling of primary roots identified 4,378 differentially expressed genes between wild type and dizzy1, revealing widespread transcriptional reprogramming. Consistent with functional enrichment analyses, histochemical and spectrophotometric assays indicated elevated reactive oxygen species and increased lignin in diz1 primary roots. These findings define dizzy1 as a pleiotropic developmental mutant linking hormone signaling, redox homeostasis, and cell wall regulation in maize growth.
Xuelian Du, Alina Klaus, Magda Alejandra Guateque Alba et al.· Frontiers in Plant Science· 0 citations
The small RNA tasiARF initiates a self-reinforcing morphogenic circuit connecting cell wall mechanics, auxin signaling, and regulated cell division to specify embryonic shoot stem cell fate, revealing how lineage-specific regulatory innovation can preserve a conserved developmental output across divergent embryonic architectures.
Qi Li, Cecilia Lara-Mondragón, A. Feller et al.· bioRxiv· 0 citations