An adenine base-editing system was established to precisely modify the sorghum SbALS gene, generating transgene-free mutant plants. These plants exhibit strong herbicide resistance, with no significant differences in agronomic traits, providing valuable germplasm for herbicide-resistance breeding in sorghum.

This commentary reviews the discovery by Yuan et al. of a conserved susceptibility module where fungal Gas2 stabilizes host SnRK1β1A to suppress nuclear immunity in rice. It discusses the mechanism for broad-spectrum resistance via genome editing and considers the essential balance between enhanced defense and associated agronomic trade-offs.

Strigolactones (SLs) are plant-specialized butenolide signaling molecules, recognized as endogenous plant hormones, that control plant development and environmental adaptation. In Arabidopsis (Arabidopsis thaliana), the repressor D53-like SMXLs regulate the expression of a vast number of genes in an EAR-motif-dependent manner to mediate SL signaling. However, it remains unclear how the SMXLs are recruited to specific genes and implement unique functions in vivo. Based on chromatin co-distribution analysis, we constructed a chromatin co-localization map of SMXL6 with 108 transcription factors. Among the candidate transcription factors, the Class II TEOSINTE BRANCHED1/CYCLOIDEA/PCF (TCP) family member TCP4 shows the highest frequency of chromatin co-localization with SMXL6. SMXL6 and TCP4 co‑localize at the promoter regions of 18 SL-induced SMXL6 target genes (SISGs), including BRC1. We confirmed that TCP4 interacts with SMXL6 and can bind directly to these co‑localized sites. The loss of CIN-TCPs function reduces the hormone responsiveness of the SL-induced genes. Introducing the tcp3/4/10 into SL‑deficient mutants restored the BRC1 expression to a level exceeding that of the wild type. However, the branching phenotype of the SL‑deficient mutant was only partially rescued, suggesting a limited role for BRC1 in SL‑mediated branching control and implicating the involvement of additional factors. An unexpected finding was that tcp3/4/10 rescued the dwarf phenotype of the SL‑deficient mutants, providing an opportunity to elucidate the mechanisms underlying SL‑regulated plant height. These findings demonstrate that TCP4 mediates SMXL6 chromatin recruitment during SL signaling, and provide a new understanding of how SMXL6 participates in SL signaling-mediated gene expression and plant development.

Floral induction in plants represents a critical developmental transition from vegetative growth to the reproductive phase, which is vital for reproductive success. Identifying new genes that control flowering time and understanding their regulatory mechanisms is crucial for improving our knowledge of plant adaptability to the environment. Here, we identify VQ motif-containing proteins VQ18 and VQ26 as novel promoters of flowering that function redundantly to regulate this process in Arabidopsis. The VQ18 and VQ26 proteins promote flowering in Arabidopsis through their interaction with the CONSTANS (CO) protein. This interaction enhances the stability of the CO protein and augments its transcriptional activation of the FLOWERING LOCUS T (FT) gene. Furthermore, VQ18 and VQ26 exhibit binding affinity for the TARGET OF EAT1 (TOE1) and TOE2 proteins, thereby diminishing the binding affinity and inhibitory effects of TOEs on FT, which alleviates the repression of flowering by TOEs. Additionally, VQ18 and VQ26 are implicated in the regulation of flowering timing by competing with TOEs for interaction with CO. Our findings broaden the functions of VQ proteins and reveal new regulatory interactions in the flowering network, providing insights into how plants balance positive and negative signals to regulate flowering time.

Editing the cucumber peroxidase gene CsPOD7 establishes a haploid inducer line capable of inducing maternal haploids.

RISBZ1 encodes the transcription factor bZIP58, which regulates grain filling; intron editing of RISBZ1 to eliminate aberrant alternatively spliced transcripts increased grain weight without compromising key agronomic traits under normal conditions, and enhanced grain weight and quality under heat stress conditions.

Ubiquitination is a central mechanism that regulates receptor kinases (RKs) in plants, where the ubiquitin code controls RK stability, endocytosis, and kinase activity, ensuring precise signaling during development and immunity. As transmembrane signaling hubs, RKs are dynamically controlled by E3 ubiquitin ligases, whose activity is itself regulated by RK phosphorylation, forming intricate feedback loops. Ubiquitination directs RKs toward degradation via either the endocytic-vacuolar or 26S proteasome pathways, with emerging evidence suggesting functional interplay between these routes. Beyond proteolysis, ubiquitination can also directly suppress RK activity. Phosphorylation of E3 ligases by activated RKs or their co-receptors modulates ligase activity, substrate binding, and ubiquitin chain linkage, enabling dynamic signal regulation. This reciprocal control establishes a sophisticated network that maintains receptor homeostasis and signaling fidelity. Despite significant progress, key questions remain about degradation pathway integration, structural mechanisms of E3-substrate-E2 complexes, and crosstalk with other post-translational modifications. Elucidating these regulatory circuits will deepen our understanding of RK-mediated cellular signaling and provide strategies to enhance crop resilience and symbiotic efficiency.

Crocins, the main active ingredients in Crocus sativus, have anti-inflammatory, antioxidant, hypolipidemic, hypoglycemic, and antitumor properties. Due to the harsh growing conditions and the limited yield of C. sativus, sustainable alternative methods for crocin production need to be explored. In this study, a new rice germplasm resource, "crocin rice", was developed by expressing eight genes of the crocin synthesis pathway in rice endosperm. The content of crocins in rice seeds was up to 9.25 μg/g dry weight, and it was also rich in a variety of carotenoids, including α-carotene, lutein, and violaxanthin. The expression of exogenous genes did not affect normal growth or the major nutritional structure of rice. Feeding experiments on mice showed that crocin rice could effectively reduce lipopolysaccharide-induced liver injury. With the adjuvant therapeutic benefits, crocin rice could be used to improve human nutrition and health. In addition, rice callus also showed the ability to synthesize crocins, which could serve as a potential substitute for C. sativus to alleviate resource shortage.