RNA interference (RNAi) is increasingly used for plant protection against pathogens and pests. However, the traditional delivery method causes plant tissue damage, is affected by environmental factors, and faces difficulties in penetrating the barriers of cell walls and the limitations of plant species, ultimately leading to low delivery efficiency. With advances in nanotechnology, nanomaterials (NMs) have been identified as effective carriers for nucleic acid delivery because of their ability to operate independently of external mechanical forces, prevent degradation by bioenzymes, exhibit good biocompatibility, and offer high loading capacity. This review summarizes the application of NM-mediated RNAi against plant pathogens and pests, focusing on how different NMs break through the cell barriers of plants, pathogens, and pests according to their size, morphology, and charge characteristics. Furthermore, we discuss the advantages and improvement strategies of NMs as nucleic acid delivery carriers, alongside assessing their potential application for the management of plant pathogens and pests.

Tomato (Solanum lycopersicum) is an important crop but frequently experiences saline–alkali stress. Our previous studies have shown that exogenous spermidine (Spd) could significantly enhance the saline–alkali resistance of tomato seedlings, in which a high concentration of Spd and jasmonic acid (JA) exerted important roles. However, the mechanism of Spd and JA accumulation remains unclear. Herein, SlWRKY42, a Group II WRKY transcription factor, was identified in response to saline–alkali stress. Overexpression of SlWRKY42 improved tomato saline–alkali tolerance. Meanwhile, SlWRKY42 knockout mutants, exhibited an opposite phenotype. RNA-sequencing data also indicated that SlWRKY42 regulated the expression of genes involved in JA signaling and Spd synthesis under saline–alkali stress. SlWRKY42 is directly bound to the promoters of SlSPDS2 and SlNHX4 to promote Spd accumulation and ionic balance, respectively. SlWRKY42 interacted with SlMYC2. Importantly, SlMYC2 is also bound to the promoter of SlSPDS2 to promote Spd accumulation and positively regulated saline–alkali tolerance. Furthermore, the interaction of SlMYC2 with SlWRKY42 boosted SlWRKY42's transcriptional activity on SlSPDS2, ultimately enhancing the tomato's saline–alkali tolerance. Overall, our findings indicated that SlWRKY42 and SlMYC2 promoted saline–alkali tolerance by the Spd biosynthesis pathway. Thus, this provides new insight into the mechanisms of plant saline–alkali tolerance responses triggered by polyamines (PAs).

Reactive oxygen species (ROS) plays critical roles in modulating plant growth and stress response and its homeostasis is fine tuned using multiple peroxidases. H₂O₂, a major kind of ROS, is removed rapidly and directly using three catalases, CAT1, CAT2, and CAT3, in Arabidopsis. Although the activity regulations of catalases have been well studied, their degradation pathway is less clear. Here, we report that CAT2 and CAT3 protein abundance was partially controlled using the 26S proteasome. To further identify candidate proteins that modulate the stability of CAT2, we performed yeast-two-hybrid screening and recovered several clones encoding a protein with RING and vWA domains, CIRP1 (CAT2 Interacting RING Protein 1). Drought and oxidative stress downregulated CIRP1 transcripts. CIRP1 harbored E3 ubiquitination activity and accelerated the degradation of CAT2 and CAT3 by direct interaction and ubiquitination. The cirp1 mutants exhibited stronger drought and oxidative stress tolerance, which was opposite to the cat2 and cat3 mutants. Genetic analysis revealed that CIRP1 acts upstream of CAT2 and CAT3 to negatively regulate drought and oxidative stress tolerance. The increased drought and oxidative stress tolerance of the cirp1 mutants was due to enhanced catalase (CAT) activities and alleviated ROS levels. Our data revealed that the CIRP1–CAT2/CAT3 module plays a vital role in alleviating ROS levels and balancing growth and stress responses in Arabidopsis.

Grain size is a key determinant of 1,000-grain weight, one of three factors determining grain yield. However, the complete regulatory network controlling grain size has not been fully clarified. Here, we identified a rice mutant, named small and round grain (srg) that exhibits semi-dwarf stature and small grain size. Cytological analysis showed that cell length and number of spikelet epidermal cells of the srg mutant are reduced, indicating that SRG controls grain size by promoting cell elongation and increasing cell number. SRG encodes a kinesin belonging to the kinesin-1 subfamily and is extensively expressed in different plant tissues with relatively high expression in young panicles. SRG protein is mainly located in the nucleus and cell membrane. Expression of the SRG gene was induced by brassinolide through the brassinosteroid (BR) responsive factor OsWRKY53 and SRG protein was phosphorylated by BR-activated kinase OsBSK3 to prevent its degradation. In addition, microtubule (MT) morphology was abnormal and disordered in the srg and cr-1 mutants. These findings suggest that BR likely stabilizes orderly assembly and arrangement of MTs by stabilizing SRG proteins, thus promoting grain size. SRG overexpression lines produced more tillers and significantly larger and heavier grains to increase 1,000-grain weight, suggesting that SRG has potential to increase grain yield. Our study indicated that SRG is a new BR responsive factor and BR might regulate grain size by influencing the expression of SRG.

Flowering time is a critical agronomic trait in rice, directly influencing grain yield and adaptability to specific planting regions and seasons. Florigens, including FLOWERING LOCUS T (FT) proteins Hd3a (OsFTL2) and RFT1 (OsFTL3), play central roles in transmitting flowering signals through rice's photoperiod regulatory network. While Hd3a and RFT1 have been extensively studied, the functions and interactions of other FT-like proteins remain unclear, limiting advancements in breeding strategies for early-maturing rice varieties. Here, we demonstrate that the florigen-like protein OsFTL1 forms a florigen activation complex (FAC) and promotes flowering under both short-day and long-day conditions. OsFTL1 localizes to the nucleus and cytoplasm, with predominant expression in the shoot base, facilitating its mobilization to the shoot apical meristem (SAM) to initiate flowering. Overexpression of OsFTL1 (OsFTL1-OE) in leaves or shoot bases significantly accelerates flowering and alters plant architecture. In the nucleus, OsFTL1 interacts with GF14c and OsFD1 to form an FAC, activating OsMADS14 and OsMADS15 expression to drive flowering. Markedly, OsFTL1-OE plants deficient in Hd3a and RFT1 exhibited earlier flowering compared with wild-type plants, indicating that OsFTL1 can independently promote flowering. Furthermore, haplotype analysis identified OsFTL1-Hap3, a beneficial variant associated with early flowering and comparable grain yields. These findings revealed that OsFTL1 can substitute for Hd3a and RFT1 in FAC formation, promoting flowering across photoperiods, and highlighting its potential application in breeding early-maturing, high-yield rice varieties suitable for diverse environments.

Increasing plant density has been recognized as an effective strategy for boosting maize yields over the past few decades. However, dense planting significantly reduces the internal light intensity and the red to far-red (R:FR) light ratio in the canopy, which subsequently triggers shade avoidance responses (SAR) that limit further yield enhancements, particularly under high-density conditions. In this study, we identified double B-box containing protein DBB2, a member of the ZmBBX family that is rapidly induced by shade, as a crucial regulator of plant height and SAR. Disruption of DBB2 resulted in shorter internodes, reduced plant height, decreased cell elongation, and diminished sensitivity to shade in maize, effects that can be largely alleviated by external treatment with gibberellins (GA). Furthermore, we discovered that DBB2 physically interacted with the transcription factor HY5, inhibiting its transcriptional activation of ZmGA2ox4, a gene encoding a GA2 oxidase that can deactivate GA. This interaction positively influences maize plant height through the GA pathway. Additionally, we found that the induction of ZmDBB2 by shade is mediated by the transcription factor PIF4. Interestingly, DBB2 then interacted with PIF4 to enhance the transcriptional activation of cell elongation-related genes, such as ZmEXPA1, thereby establishing a positive feedback loop promoting cell elongation under canopy shade conditions. Our findings highlight the critical role of BBX proteins in modulating plant height and SAR, presenting them as key genetic targets for developing maize varieties suited to high-density planting conditions. This study also provides new insights into the molecular mechanisms underlying SAR and offers potential strategies for the genetic improvement of maize plant architecture and grain yield.

Jasmonic acid (JA) and gibberellin (GA) coordinate many aspects of plant growth and development, including anthocyanin biosynthesis. However, the crossover points of JA and GA signals and the pathways through which they interact to regulate anthocyanin biosynthesis are poorly understood. Here, we investigated the molecular mechanism by which the zinc finger protein (ZFP) transcription factor Malus domestica ZFP7 (MdZFP7) regulates anthocyanin biosynthesis by integrating JA and GA signals at the transcriptional and post-translational levels. MdZFP7 is a positive regulator of anthocyanin biosynthesis, which fulfills its role by directly activating the expression of MdMYB1 and enhancing the transcriptional activation of MdWRKY6 on the target genes MdDFR and MdUF3GT. MdZFP7 integrates JA and GA signals by interacting with the JA repressor apple JASMONATE ZIM-DOMAIN2 (MdJAZ2) and the GA repressor apple REPRESSOR-of-ga1-3-like 3a (MdRGL3a). MdJAZ2 weakens the transcriptional activation of MdMYB1 by MdZFP7 and disrupts the MdZFP7–MdWRKY6 interaction, thereby reducing the anthocyanin biosynthesis promoted by MdZFP7. MdRGL3a contributes to the stimulation of anthocyanin biosynthesis by MdZFP7 by sequestering MdJAZ2 from the MdJAZ2–MdZFP7 complex. The E3 ubiquitin ligase apple BOI-related E3 ubiquitin-protein ligase 3 (MdBRG3), which is antagonistically regulated by JA and GA, targets the ubiquitination degradation of MdZFP7. The MdBRG3-MdZFP7 module moves the crosstalk of JA and GA signals from the realm of transcriptional regulation and into the protein post-translational modification. In conclusion, this study not only elucidates the node-role of MdZFP7 in the integration of JA and GA signals, but also describes the transcriptional and post-translational regulatory network of anthocyanin biosynthesis with MdZFP7 as the hub.

Seed color is a key agronomic trait in crops such as peanut, where it is a vital indicator of both nutritional and commercial value. In recent years, peanuts with darker seed coats have gained market attention due to their high anthocyanin content. Here, we used bulk segregant analysis to identify the gene associated with the purplish-red coat trait and identified a novel gene encoding a basic/helix–loop–helix transcription factor, PURPLE RED SEED COAT1 (PSC1), which regulates the accumulation of anthocyanins in the seed coat. Specifically, we found that a 35-bp insertion in the PSC1 promoter increased the abundance of PSC1 mRNA. Transcriptomic and metabolomic analyses indicated that the purplish-red color of the seed coat was the result of decreased expression of anthocyanidin reductase (ANR), leading to increased accumulation of delphinidin, cyanidin, and pelargonidin derivatives. Further analysis revealed that PSC1 interacts with AhMYB7 to form a complex that specifically binds to the ANR promoter to suppress its expression, resulting in increased anthocyanin accumulation. Moreover, overexpression of PSC1 increased anthocyanin content in Arabidopsis thaliana and peanut callus. Our study reveals a new gene that controls seed coat color by regulating anthocyanin metabolism and provides a valuable genetic resource for breeding peanuts with a purplish-red seed coat.

Incorporating genotype-by-environment (GE) interaction effects into genomic prediction (GP) models with multi-environment climate data can improve selection accuracy to accelerate crop breeding but has received little research attention. Here, we conducted a cross-region GP study of grain moisture content (GMC) and grain yield (GY) in maize hybrids in two major Chinese growing regions using data for 19 climatic factors across 34 environments in 2020 and 2021. Predictions were conducted in 2,126 hybrids generated from 475 maize inbred lines, using 9,355 single nucleotide polymorphism markers for genotyping. Models based on genomic best linear unbiased prediction (GBLUP) incorporating GE interaction effects of 19 climatic factors associated with day length, transpiration, temperature, and radiation (GBLUP-GE_19CF) trained on whole data set outperformed the traditional GBLUP or BayesB models in predicting GMC or GY by 10-fold cross-validation, achieving prediction accuracies of 0.731 and 0.331, respectively. To refine the climate data, we examined 84 statistical features associated with these climatic factors and identified nine factors most correlated with GMC or GY. Principal component analysis of climate data yielded nine principal components responsible for 97% of the variability in the data. Incorporating these nine factors or principal components into the GBLUP-GE framework with a similarity matrix of environments (GBLUP-GE_9CF and GBLUP-GE_PCA) provided similar prediction accuracies but could reduce the computational burden. In addition, increasing the number of test set environments in the training set from 8 to 14 increased the prediction accuracy of GBLUP-GE_19CF trained with monthly average climate data for 2020–2021. Examining prediction accuracy based on concordance, the proportion of overlapping hybrids between the top 50% of predicted and observed values for GMC and GY, indicated that concordance exceeded 50% for the GBLUP-GE_19CF model, confirming the reliability of our predictions. This study can provide practical guidance for optimizing GPs for maize breeding programs in multi-environment selection.

Heat stress (HS) at the reproductive stage detrimentally affects crop yields and seed quality. However, the molecular mechanisms that protect reproductive processes in plants under HS remain largely unknown. Here, we report that Acetylation Lowers Binding Affinity 3 (ALBA3) is crucial for safeguarding male fertility against HS in Arabidopsis. ALBA3 is highly expressed in pollen, and ALBA3 is localized in the cytoplasm of both sperm and vegetative cells. Mutants lacking functional ALBA3 exhibit hypersensitivity to HS, with reduced silique length and fertility due to defects in pollen germination, pollination, pollen tube growth, and fertilization under HS. ALBA3 binds and stabilizes a subset of messenger RNAs (mRNAs) essential for pollen function, thereby protecting male fertility. Two residues in the Alba domain, K46 and L90, are critical for ALBA3's ability to bind and stabilize mRNAs and are necessary for its proper function. Interestingly, the loss of rice ALBA3 also leads to severe pollen abortion and male sterility under HS, highlighting the conserved role of ALBA3 in protecting male fertility across plant species. This study uncovers a conserved mechanism by which ALBA3 safeguards male fertility during HS by stabilizing specific mRNAs crucial for pollen function.