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Some peroxidases (PRXs) are involved in abiotic stress response. However, to the best of our knowledge, the effects of PRXs on agronomic traits including grain number per spike (GNS), spikelet number per spike (SNS) and spike length (SL) are also largely unknown. In our study, we cloned a wheat PRX gene TaPRX -2A and identified its function in controlling GNS by generating transgenic overexpression lines. The results showed that TaPRX-2A overexpression displayed lower GNS and shorter SL, compared with the wild-type plants. RNA-seq analysis indicated alterations in various pathways including flavonoid biosynthesis, lignin biosynthesis, phytohormone signaling, as well as sucrose and starch biosynthesis. Co-expression analysis showed that transcription factors, such as bHLH, WRKY, and bZIP may be involved in the regulation of various genes associated with these pathways. Our findings provide insights into the mechanisms by which PRXs regulate agronomic traits, illustrating potential applicability in crop improvement programs. [ABSTRACT FROM AUTHOR]

The wall-associated kinase (WAK) gene family encodes functional cell wall-related proteins. These genes are widely presented in plants and serve as the receptors of plant cell membranes, which perceive the external environment changes and activate signaling pathways to participate in plant growth, development, defense, and stress response. However, the WAK gene family and the encoded proteins in soybean (Glycine max (L.) Merr) have not been systematically investigated. In this study, the soybean WAK genes (GmWAK) were identified based on genome-wide sequence information, the basic characteristics, chromosome location, gene replication, expression pattern, and responses to stress were comprehensively analyzed. A total of 74 GmWAK genes were identified and mapped to 19 different chromosomes in the soybean genome. Seventy-four GmWAK genes were divided into four groups, and GmWAK genes in the same group shared similar gene structures and conserved motifs. Thirty-seven duplicate pairs were identified in 74 GmWAK genes. Segmental duplication (SD) was critical in soybean WAK gene family expansion, and purification selection occurred during evolution. The promoter cis-element analysis displayed many hormone- and stress-related response elements in the promoter regions of GmWAK genes. GmWAK genes were diversely expressed in different organs and tissues, with most actively responding to cold, heat, salt, drought, and heavy metal stresses, suggesting that GmWAK genes could exhibit relevant roles in various bioprocesses. [ABSTRACT FROM AUTHOR]

Melatonin (MT) serves an indispensable function in plant development and their response to abiotic stress. Although numerous drought‐tolerance genes have been ascertained in wheat, further investigation into the molecular pathways controlling drought stress tolerance remains necessary. In this investigation, it was observed that MT treatment markedly enhanced drought resistance in wheat by diminishing malondialdehyde (MDA) levels and augmenting the activity of antioxidant enzymes POD, APX, and CAT compared to untreated control plants. Transcriptomic analysis disclosed that melatonin treatment activated the tryptophan metabolism and flavonoid biosynthesis pathways. Furthermore, quantitative reverse transcription PCR (qRT‐PCR) outcomes validated that the expression trends of these differentially expressed genes aligned with the transcriptomic data. Metabolomic profiling identified alterations in the abundance of several metabolites, including tryptamine, MT, formylanthranilate, 3‐hydroxyanthranilate, 6‐hydroxymelatonin, naringenin chalcone, astragalin, pinbanksin, and caffeoyl quinic acid. Co‐expression analysis suggested that various transcription factors—encompassing AP2/ERF‐ERF, WRKY, bZIP, C2H2, bHLH, NAC, and MYB—participated in controlling the differentially expressed genes across multiple pathways. Ultimately, these findings highlight that exogenous MT application bolsters wheat's drought tolerance through the modulation of tryptophan metabolism and flavonoid biosynthesis. These insights provide novel perspectives on the molecular frameworks mediating MT's effect on drought resistance and pinpointing candidate genes for potential genetic enhancement programs in wheat. [ABSTRACT FROM AUTHOR]

Wheat is one of the most crucial food crops globally, with its yield directly impacting global food security. The accurate detection and counting of wheat spikes is essential for monitoring wheat growth, predicting yield, and managing fields. However, the current methods face challenges, such as spike size variation, shading, weed interference, and dense distribution. Conventional machine learning approaches have partially addressed these challenges, yet they are hampered by limited detection accuracy, complexities in feature extraction, and poor robustness under complex field conditions. In this paper, we propose an improved YOLOv10 algorithm that significantly enhances the model's feature extraction and detection capabilities. This is achieved by introducing a bidirectional feature pyramid network (BiFPN), a separated and enhancement attention module (SEAM), and a global context network (GCNet). BiFPN leverages both top-down and bottom-up bidirectional paths to achieve multi-scale feature fusion, improving performance in detecting targets of various scales. SEAM enhances feature representation quality and model performance in complex environments by separately augmenting the attention mechanism for channel and spatial features. GCNet captures long-range dependencies in the image through the global context block, enabling the model to process complex information more accurately. The experimental results demonstrate that our method achieved a precision of 93.69%, a recall of 91.70%, and a mean average precision (mAP) of 95.10% in wheat spike detection, outperforming the benchmark YOLOv10 model by 2.02% in precision, 2.92% in recall, and 1.56% in mAP. Additionally, the coefficient of determination (R2) between the detected and manually counted wheat spikes was 0.96, with a mean absolute error (MAE) of 3.57 and a root-mean-square error (RMSE) of 4.09, indicating strong correlation and high accuracy. The improved YOLOv10 algorithm effectively solves the difficult problem of wheat spike detection under complex field conditions, providing strong support for agricultural production and research. [ABSTRACT FROM AUTHOR]

Fusarium head blight (FHB) caused by Fusarium graminearum Schwabe (teleomorph Gibberella zeae (Schw.) Perch) results in large yield losses in annual global wheat production. Although studies have identified a number of wheat FHB resistance genes, a deeper understanding of the mechanisms underlying host plant resistance to F. graminearum is required for the control of FHB. Here, an integrated metabolomics and transcriptomics analysis of infected wheat plants (Triticum aestivum L.) enabled identification of 789 differentially accumulated metabolites, including flavonoids, phenolamides, tryptamine derivatives, and phytohormones, and revealed altered expression of more than 100 genes that function in the biosynthesis or regulation of these pathways. Our data regarding the effects of F. graminearum infection on flavonoids and auxin signaling led to follow‐up experiments that showed that exogenous kaempferide and apigenin application on spikes increased wheat resistance to FHB, while exogenous auxin treatment increased FHB susceptibility. RNAi‐mediated knockdown of the gene encoding the auxin receptor, TaTIR1, increased FHB resistance. Our data supported the use of TaTIR1 knockdown in controlling FHB. Our study provides insights on the wheat response to F. graminearum infection and its FHB resistance mechanisms while illustrating the potential of TaTIR1 knockdown in increasing FHB resistance during crop improvement programs. [ABSTRACT FROM AUTHOR]

Key message: TaUGT5: can reduce the proliferation and destruction of F. graminearum and enhance the ability of FHB resistance in wheat.Abstract: Deoxynivalenol (DON) is one of the most important toxins produced by Fusarium species that enhances the spread of the pathogen in the host. As a defense, the UDP-glycosyltransferase (UGT) family has been deduced to transform DON into the less toxic form DON-3-O-glucoside (D3G), but the specific gene member in wheat that is responsible for Fusarium head blight (FHB) resistance has been little investigated and proved. In this study, a DON and Fusarium graminearum responsive gene TaUGT5, which is specific for resistant cultivars, was cloned with a 1431 bp open reading frame (ORF) encoding 476 amino acids in Sumai3. TaUGT5 is located on chromosome 2B, which has been confirmed in nulli-tetrasomic lines of Chinese Spring (CS) and is solely expressed among three homologs on the A, B and D genomes. Over-expression of this gene in Arabidopsis conferred enhanced tolerance when grown on agar plates that contain DON. Similarly, the coleoptiles of wheat over-expressing TaUGT5 showed more resistance to F. graminearum, evidencing reduced proliferation and destruction of plant tissue by the pathogen. However, the disease resistance in spikes was not as significant as that on coleoptile compared with wild-type plants. A subcellular localization analysis revealed that TaUGT5 was localized on the plasma membrane of tobacco leaf epidermal cells. It is possible that TaUGT5 could enhance tolerance to DON, protect the plant cell from the pathogen infection and result in better maintenance of the cell structure, which slows down pathogen proliferation in plant tissue. [ABSTRACT FROM AUTHOR]

Fusarium head blight (FHB), a fungal disease caused by Fusarium species that produce food toxins, currently devastates wheat production worldwide, yet few resistance resources have been discovered in wheat germplasm. Here, we cloned the FHB resistance gene Fhb7 by assembling the genome of Thinopyrum elongatum , a species used in wheat distant hybridization breeding. Fhb7 encodes a glutathione S-transferase (GST) and confers broad resistance to Fusarium species by detoxifying trichothecenes through de-epoxidation. Fhb7 GST homologs are absent in plants, and our evidence supports that Th. elongatum has gained Fhb7 through horizontal gene transfer (HGT) from an endophytic Epichloë species. Fhb7 introgressions in wheat confers resistance to both FHB and crown rot in diverse wheat backgrounds without yield penalty, providing a solution for Fusarium resistance breeding., (Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.)