Maize (Zea mays) originated in southern Mexico and has spread over a wide latitudinal range. Maize expansion from tropical to temperate regions has necessitated a reduction of its photoperiod sensitivity. In this study, we cloned a quantitative trait locus (QTL) regulating flowering time in maize and show that the maize ortholog of Arabidopsis thaliana EARLY FLOWERING3, ZmELF3.1, is the causal locus. We demonstrate that ZmELF3.1 and ZmELF3.2 proteins can physically interact with ZmELF4.1/4.2 and ZmLUX1/2, to form evening complex(es; ECs) in the maize circadian clock. Loss-of-function mutants for ZmELF3.1/3.2 and ZmLUX1/2 exhibited delayed flowering under long-day and short-day conditions. We show that EC directly represses the expression of several flowering suppressor genes, such as the CONSTANS, CONSTANS-LIKE, TOC1 (CCT) genes ZmCCT9 and ZmCCT10, ZmCONSTANS-LIKE 3, and the PSEUDORESPONSE REGULATOR (PRR) genes ZmPRR37a and ZmPRR73, thus alleviating their inhibition, allowing florigen gene expression and promoting flowering. Further, we identify two closely linked retrotransposons located in the ZmELF3.1 promoter that regulate the expression levels of ZmELF3.1 and may have been positively selected during postdomestication spread of maize from tropical to temperate regions during the pre-Columbian era. These findings provide insights into circadian clock-mediated regulation of photoperiodic flowering in maize and new targets of genetic improvement for breeding.

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.

A dual-substrate X-ray CT platform using high-contrast media and modular scanning overcomes traditional resolution and size limits to enable large-scale, high-resolution 3D in situ root phenotyping.