Rubus sachalinensis, a Mongolian medicinal plant, serves as a valuable raspberry breeding resource due to its high value and stress resistance. Global climate change and human logging have contributed to its gradual decline in population. In this study, we utilized MaxEnt modeling to forecast the potential distribution of suitable habitat for R. sachalinensis under changing climatic conditions, aiming to facilitate controlled cultivation to lessen dependence on wild populations and support conservation efforts. In this study, by integrating 573 global distribution records of R. sachalinensis with 22 environmental variables related to climate and terrain, we developed the MaxEnt model and selected 11 variables based on the correlation (correlation threshold r < 0.8) for analysis. Through the jackknife method, we found that the distribution of R. sachalinensis is primarily influenced by precipitation during the warmest quarter (bio18, 43%), mean temperature of the coldest quarter (bio11, 20.5%), temperature seasonality (bio4, 17.1%), and slope (12.2%). The habitat of R. sachalinensis reached its maximum extent during the Last Interglacial period, subsequently decreased, and then expanded to 4726.25 × 10³ km² during the Mid-Holocene period, and currently stands at 5293.45 × 10³ km² in northeastern China, eastern Mongolia, and southeastern Russia, with a smaller distribution in North America, particularly in western Canada. Future projections indicated a declining trend in SSP1_2.6 and SSP5_8.5, with the centroid expected to shift eastward. Consequently, due to environmental changes, the suitable habitat distribution of R. sachalinensis will shift eastward, leading to a reduction in habitat area, and human logging will further exacerbate the reduction in wild resources. The resources within the area that remain constant from the ancient climate period to the future suitable habitat should be strengthened for protection, as well as the resources in the shrinking areas. These findings provide potential distribution information and dynamic changes in R. sachalinensis, which will provide vital data for identifying important conservation areas and sustainable harvesting.

GmSRC7 is a broad-spectrum antiviral R gene from soybean, but its downstream and functionally related genes remain unclear. Virus-induced gene silencing (VIGS) assays in Nicotiana benthamiana (Nb) showed that suppression of several gene families—WRKY transcription factors, chaperones, ethylene pathway components, MAPK cascade elements, salicylic acid (SA) signaling genes, calcium-dependent protein kinases, nuclear migration proteins, RNA replication-related genes, and immune regulators—consistently weakened GmSRC7-mediated resistance to Soybean Mosaic Virus (SMV) and Tobacco Mosaic Virus (TMV). Targeted silencing of four regulatory genes—NbEDS1, NbARF1, NbSGT1, and NbCOI1—markedly enhanced GmSRC7-mediated resistance to SMV and TMV in our experiments. Silencing the serine/threonine kinase gene NbPBS1 increased GmSRC7-conferred resistance to SMV but did not significantly alter its resistance to TMV. Transient expression assays showed that NbARF1, NbSGT1, and NbCOI1 antagonize GmSRC7-mediated defense against SMV and TMV, whereas NbPBS1 specifically suppresses anti-SMV activity without affecting TMV resistance. Transient overexpression of SA-degrading enzymes (AtS3H, AtS5H, and NahG) significantly reduced GmSRC7-conferred resistance to SMV, indicating that SA is essential for this R protein-mediated defense. Genes were also grouped by immune pathways and function: co-expression of chaperone family genes inhibited GmSRC7 activity against SMV and TMV, while co-expression of WRKY family genes enhanced anti-SMV activity of GmSRC7. Finally, transient silencing of soybean genes GmEDS1, GmSGT1-1, GmSGT1-2, GmJAR1, and GmSGS3 compromised GmSRC7-mediated resistance to SMV.

Populus hopeiensis is an important native poplar species in northern China, but herbivorous insect damage seriously affects its growth and ecological function. WRKY transcription factors play important roles in plant stress responses; however, the function of WRKY23 homologs in woody plant resistance to chewing herbivores remains unclear. In this study, a herbivore-responsive WRKY transcription factor gene, PhWRKY23, was identified from P. hopeiensis. PhWRKY23 expression was significantly induced by Spodoptera litura feeding, with a maximum increase of approximately 69.71-fold the control level at the highest damage level, and the encoded protein was predominantly localized in the nucleus. To investigate its function, PhWRKY23-overexpressing and RNA interference transgenic lines were generated. In the choice feeding assay, the consumed leaf area of PhWRKY23-overexpressing plants was approximately 85.5% lower than that of WT plants after 8 h. In the no-choice feeding assay, the total larval mass after 6 d was approximately 38.8% lower in larvae fed on overexpression plants and 51.0% higher in larvae fed on RNAi plants than in those fed on WT plants. Physiological analysis showed that RNAi plants accumulated significantly more MDA than WT and overexpression plants, whereas overexpression plants had higher chlorophyll a, chlorophyll b, and carotenoid contents than the other genotypes. Phytohormone analysis further showed that PhWRKY23-overexpressing plants accumulated higher levels of jasmonic acid, jasmonoyl-L-isoleucine, and salicylic acid, whereas abscisic acid showed no significant difference among genotypes. Yeast two-hybrid screening identified several candidate PhWRKY23-interacting proteins, and pairwise validation confirmed that PhWRKY23 interacted with PhDOX1 in yeast. These results indicate that PhWRKY23 positively contributes to herbivore resistance in P. hopeiensis and that this resistance phenotype is associated with changes in JA, JA-Ile, and SA accumulation and defense-related physiological traits.

Cucurbitacins are highly oxygenated tetracyclic triterpenoids characterized by intense bitterness, substantial structural diversity, and important consequences for plant–herbivore interactions. Although best known from Cucurbitaceae, cucurbitacins and related cucurbitane-type metabolites also occur in phylogenetically distant herbaceous and woody plants. Genetic and biochemical studies have validated several core biosynthetic steps, including cucurbitadienol formation by oxidosqualene cyclases and subsequent modification by cytochrome P450 monooxygenases, acyltransferases, and glycosyltransferases. Tissue-preferential basic helix–loop–helix transcription factors constitute the best-characterized regulatory layer, whereas the evidence supporting accessory regulators, transporters, and environmental responses varies from functional validation to transcriptomic or genomic prediction. From the plant perspective, cucurbitacins deter feeding or impair performance in many generalist and non-adapted herbivores. By contrast, their use as host-recognition cues and feeding stimulants by specialist diabroticite beetles reflects evolved herbivore adaptations involving perception, tolerance, metabolism, or sequestration rather than a second defensive function of the plant trait. Herbivore-induced cucurbitacin accumulation has been demonstrated in particular systems, although its regulatory mechanisms and ecological generality remain unresolved. Unlike previous reviews centered primarily on cucurbitacin chemistry, pharmacological activity, or individual biosynthetic pathways, this review integrates evidence-graded pathway reconstruction and molecular regulation with taxonomic distribution, insect adaptation, domestication, and agroecological consequences. Mechanistically, this review traces how scaffold formation, oxidative tailoring, conjugation, tissue-specific regulation, and transport give rise to contrasting ecological outcomes through herbivore-specific perception, tolerance, metabolism, and sequestration. We conclude that uniformly increasing or eliminating cucurbitacins is unlikely to provide broadly effective crop resistance because either direction may favor a different herbivore group. Future priorities include functional validation of candidate genes, spatially resolved metabolite analysis, comparative investigation of non-cucurbit lineages, and field evaluation involving generalist and specialist herbivores, crop quality, and non-target organisms. These advances will support context-specific fruit-quality improvement, behavioral pest control, and integrated pest management strategies rather than cucurbitacin manipulation as a stand-alone resistance approach.