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Summary: Seed vigour, including rapid, uniform germination and robust seedling establishment under various field conditions, is becoming an increasingly essential agronomic trait for achieving high yield in crops. However, little is known about this important seed quality trait. In this study, we performed a genome‐wide association study to identify a key transcription factor ZmRap2.7, which regulates seed vigour through transcriptionally repressing expressions of three ABA signalling genes ZmPYL3, ZmPP2C and ZmABI5 and two phosphatidylethanolamine‐binding genes ZCN9 and ZCN10. In addition, ZCN9 and ZCN10 proteins could interact with ZmPYL3, ZmPP2C and ZmABI5 proteins, and loss‐of‐function of ZmRap2.7 and overexpression of ZCN9 and ZCN10 reduced ABA sensitivity and seed vigour, suggesting a complex regulatory network for regulation of ABA signalling mediated seed vigour. Finally, we showed that four SNPs in ZmRap2.7 coding region influenced its transcriptionally binding activity to the downstream gene promoters. Together with previously identified functional variants within and surrounding ZmRap2.7, we concluded that the distinct allelic variations of ZmRap2.7 were obtained independently during maize domestication and improvement, and responded separately for the diversities of seed vigour, flowering time and brace root development. These results provide novel genes, a new regulatory network and an evolutional mechanism for understanding the molecular mechanism of seed vigour. [ABSTRACT FROM AUTHOR]

Effective in-season crop nitrogen (N) status diagnosis is important for precision crop N management, and remote sensing using an unmanned aerial vehicle (UAV) is one efficient means of conducting crop N nutrient diagnosis. Here, field experiments were conducted with six N levels and six maize hybrids to determine the nitrogen nutrition index (NNI) and yield, and to diagnose the N status of the hybrids combined with multi-spectral data. The NNI threshold values varied with hybrids and years, ranging from 0.99 to 1.17 in 2018 and 0.60 to 0.71 in 2019. A proper agronomic optimal N rate (AONR) was constructed and confirmed based on the measured NNI and yield. The NNI (R2 = 0.64–0.79) and grain yield (R2 = 0.70–0.73) were predicted well across hybrids using a random forest model with spectral, structural, and textural data (UAV). The AONRs calculated using the predicted NNI and yield were significantly correlated with the measured NNI (R2 = 0.70 and 0.71 in 2018 and 2019, respectively) and yield (R2 = 0.68 and 0.54 in 2018 and 2019, respectively). It is concluded that data fusion can improve in-season N status diagnosis for different maize hybrids compared to using only spectral data. [ABSTRACT FROM AUTHOR]

Maize (Zea mays L.) has undergone profound changes in root anatomy for environmental adaptation during domestication. However, the genetic mechanism of plasticity of maize root anatomy during the domestication process remains unclear. In this study, high-resolution mapping was performed for nine root anatomical traits using a maize-teosinte population (mexicana × Mo17) across three environments. Large genetic variations were detected for different root anatomical traits. The cortex, stele, aerenchyma areas, xylem vessel number, and cortical cell number had large variations across three environments, indicating high plasticity. Sixteen quantitative trait loci (QTL) were identified, including seven QTL with QTL × environment interaction (EIQTL) for high plasticity traits and nine QTL without QTL × environment interaction (SQTL). Most of the root loci were consistent with shoot QTL depicting domestication signals. Combining transcriptome and genome-wide association studies revealed that AUXIN EFFLUX CARRIER PIN–FORMED LIKE 4 (ZmPILS4) serves as a candidate gene underlying a major QTL of xylem traits. The near-isogenic lines (NILs) with lower expression of ZmPILS4 had 18–24% more auxin concentration in the root tips and 8–15% more xylem vessels. Nucleotide diversity values analysis in the promoter region suggested that ZmPILS4 was involved in maize domestication and adaptation. These results revealed the potential genetic basis of root anatomical plasticity during domestication. [ABSTRACT FROM AUTHOR]

Summary: Phytol is one of the key precursors for tocopherol synthesis in plants, however, the underlying mechanisms concerning the accumulation of tocopherol remain poorly understood. In this study, qVE5, a major QTL affecting tocopherol accumulation in maize kernels was identified via a positional cloning approach. qVE5 encodes a protochlorophyllide oxidoreductase (ZmPORB2), which localizes to the chloroplast. Overexpression of ZmPORB2 increased tocopherol content in both leaves and kernels. Candidate gene association analysis identified a 5/8‐bp insertion/deletion (InDel058) in the 5′ untranslated region (UTR) as the causal polymorphism in affecting ZmPORB2 expression and being highly associated with tocopherol content. We showed that higher expression of ZmPORB2 correlated with more chlorophyll metabolites in the leaf following pollination. RNA‐sequencing and metabolic analysis in near isogenic lines (NILs) support that ZmPORB2 participates in chlorophyll metabolism enabling the production of phytol, an important precursor of tocopherol. We also found that the tocopherol content in the kernel is mainly determined by the maternal genotype, a fact that was further confirmed by in vitro culture experiments. Finally, a PCR‐based marker based on Indel058 was developed in order to facilitate the high tocopherol (vitamin E) maize breeding. Significance Statement: Known as vitamin E, tocopherol is a lipid‐soluble antioxidant required for plant growth and human health. In this study, characterization of ZmPORB2 involved in chlorophyll metabolism revealed that this gene affects tocopherol content in maize by the maternal genotype and has applicable potential in breeding. [ABSTRACT FROM AUTHOR]

Long non‐coding RNAs (lncRNAs), whose sequences are approximately 200 bp or longer and unlikely to encode proteins, may play an important role in eukaryotic gene regulation. Although the latest maize (Zea mays L.) reference genome provides an essential genomic resource, genome‐wide annotations of maize lncRNAs have not been updated. Here, we report on a large transcriptomic dataset collected from 749 RNA sequencing experiments across different tissues and stages of the maize reference inbred B73 line and 60 from its wild relative teosinte. We identified 18,165 high‐confidence lncRNAs in maize, of which 6,873 are conserved between maize and teosinte. We uncovered distinct genomic characteristics of conserved lncRNAs, non‐conserved lncRNAs, and protein‐coding transcripts. Intriguingly, Shannon entropy analysis showed that conserved lncRNAs are likely to be expressed similarly to protein‐coding transcripts. Co‐expression network analysis revealed significant variation in the degree of co‐expression. Furthermore, selection analysis indicated that conserved lncRNAs are more likely than non‐conserved lncRNAs to be located in regions subject to recent selection, indicating evolutionary differentiation. Our results provide the latest genome‐wide annotation and analysis of maize lncRNAs and uncover potential functional divergence between protein‐coding, conserved lncRNA, and non‐conserved lncRNA genes, demonstrating the high complexity of the maize transcriptome. Long noncoding RNAs have been reckoned as "transcription noise" or "junk sequences" for a long time. However, a big transcriptome dataset of maize and its relative teosinte demonstrated that long noncoding RNAs are largely involved in the regulation of plant development and evolution. [ABSTRACT FROM AUTHOR]