In grain crops such as maize (Zea mays), leaf angle (LA) is a key agronomic trait affecting light interception and thus planting density and yield. Nitrogen (N) affects LA in plants, but we lack a good understanding of how N regulates LA. Here, we report that N deficiency enhanced lignin deposition in the ligular region of maize seedlings. In situ hybridization showed that the bZIP transcription factor gene ZmbZIP27 is mainly expressed in the phloem of maize vascular bundles. Under N-sufficient conditions, transgenic maize overexpressing ZmbZIP27 showed significantly smaller LA compared with wild type (WT). By contrast, mutant showed larger LA under both N-deficient and N-sufficient conditions compared with WT. Overexpression of ZmbZIP27 enhanced lignin deposition in the ligular region of maize in the field. We further demonstrated that ZmbZIP27 could directly bind the promoters of the microRNA genes ZmMIR528a and ZmMIR528b and negatively regulate the expression levels of ZmmiR528. ZmmiR528 knockdown transgenic maize displayed erect architecture in the field by increasing lignin content in the ligular region of maize. Taken together, these results indicate that ZmbZIP27 regulates N-mediated LA size by regulating the expression of ZmmiR528 and modulating lignin deposition in maize.

Conventional peptides (CPs) and non-conventional peptides (NCPs) are generated from small open reading frames, but most CPs are derived from large precursors. NCPs, which are derived from sequences other than conventional open reading frames or annotated coding sequences regions, function in plant development and adaptation to stresses. Ribosome profiling, a technique for studying translational regulation, can be used to identify NCPs. Another new technique, peptidogenomics, which integrates mass spectrometry and genomics, is becoming more widely used for identifying plant NCPs. In recent years, numerous studies have investigated the roles in monocots and dicots of miRNA-derived peptides and upstream open reading frames, which have potential for improving agronomic traits. Investigating the biological functions of NCPs will advance molecular plant breeding by identifying regulators of plant growth and development. We present an overview of NCP identification methods and recent findings about NCP biological functions.

Lodging is a major problem limiting maize yield worldwide. However, the mechanisms of lodging resistance remain incompletely understood for maize. Here, we evaluated 443 maize accessions for lodging resistance in the field. Five lodging-resistant accessions and five lodging-sensitive accessions were selected for further research. The leaf number, plant height, stem diameter, and rind penetrometer resistance were similar between lodging-resistant and -sensitive inbred lines. The average thickness of sclerenchymatous hypodermis layer was thicker and the vascular area was larger in the lodging-resistant lines compared with lodging-sensitive lines. Although total lignin content in stem tissue did not significantly differ between lodging-resistant and -sensitive lines, phloroglucinol staining revealed that the lignin content of the cell wall in the stem cortex and in the stem vascular tissue near the cortex was higher in the lodging-resistant lines than in the lodging-sensitive lines. Analysis of strand-specific RNA-seq transcriptome showed that a total of 793 genes were up-regulated and 713 genes were down-regulated in lodging-resistant lines relative to lodging-sensitive lines. The up-regulated genes in lodging-resistant lines were enriched in cell wall biogenesis. These results indicated that modification of cell wall biosynthesis would contribute to lodging resistance of maize.