The YABBY transcription factor family plays a critical role in the development of lateral organs and the establishment of polarity in plants. However, its evolutionary dynamics and regulatory functions in response to abiotic stress in maize (Zea mays) remain unclear. In this study, we conducted a genome-wide analysis of the maize YABBY gene family, employing phylogenetic analysis, transcriptomics, co-expression networks, and molecular experiments. A total of 12 ZmYABBY genes were identified from 26 maize inbred lines and classified into five conserved subfamilies. Evolutionary analysis indicated that the family is structurally stable, predominantly shaped by purifying selection, with limited lineage-specific variation among hybrid populations, highlighting its high evolutionary conservation. In contrast, transcriptomic analysis revealed functional diversification: ZmYABBY genes were preferentially expressed in floral organs and exhibited distinct response patterns under drought and heat stress. Notably, co-expression network analysis identified ZmYABBY8 as a hub gene that was significantly induced under drought stress, as validated by RT-qPCR. Furthermore, its promoter region was found to be enriched with conserved stress-responsive cis-elements, including ABRE and DRE. Subcellular localization further confirmed that ZmYABBY8 is localized to the nucleus. In summary, the maize YABBY gene family is evolutionarily conserved yet functionally diversified, with ZmYABBY8 acting as a potential hub linking development and stress responses, making it a promising candidate for improving stress tolerance in maize.

Soil compaction poses a significant challenge in modern agriculture, as it constrains root development and hinders crop growth. The increasing evidence indicated that various phytohormones collaborate in distinct root zones to regulate root growth in compacted soils. However, the study of root development in maize under such conditions has been relatively limited. Here, we identified that the ZmSPL12 gene, belonging to the SPL transcription factor family, plays a crucial and positive role in regulating root development in the compacted soil. Specifically, the overexpression of ZmSPL12 resulted in significantly less inhibition of root growth than the wild-type plants when subjected to soil compaction. Histological analysis revealed that the capacity for root growth in compacted soil is closely associated with the development of the root cap. Further exploration demonstrated that ZmSPL12 modulates root growth through regulating ethylene signaling. Our findings underscored that ZmSPL12 expression level is induced by soil compaction and then enhances root penetration by regulating root cap and development, thereby enabling roots to thrive better in the compacted soil environment.

Nitrogen use efficiency (NUE) is a major determinant of maize (Zea mays L.) productivity and sustainability, yet the regulatory changes associated with modern breeding remain incompletely understood. Here, we used breeding-era transcriptomic data from 137 elite Chinese maize inbred lines to identify transcriptional regulators associated with maize NUE. Breeding-era expression shifts in NUE effector genes were modest but tissue-specific, pointing to pathway-level transcriptional rewiring during modern breeding. Focusing on the first leaf above the uppermost ear at silking, we identified 69 breeding-era-responsive genes, including 10 transcription factors, and prioritized ZmSPL19 through Pearson correlation analysis with curated NUE-related genes. ZmSPL19 expression declined during modern breeding and showed a nitrate-repressed expression, with lower transcript abundance under nitrogen-sufficient conditions and rapid downregulation upon nitrate resupply. Loss of ZmSPL19 function promoted primary root elongation, biomass accumulation, leaf nitrogen content, soil–plant analysis development (SPAD), photosynthetic rate, kernel number, and grain yield under nitrogen-sufficient conditions. These results identify ZmSPL19 as a breeding-associated negative regulator of growth and yield formation under nitrogen-sufficient conditions and support the value of a breeding-informed strategy for discovering regulators with potential relevance to maize NUE improvement.