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Review Open access Aug 2026

Leveraging transcriptional, genomic, and epigenetic regulatory layers to enhance abiotic stress resilience in grapevine

Grapevine (Vitis vinifera), an industry valued at approximately 108.61 billion US dollars globally, faces escalating threats from abiotic stresses that intensify under climate change and increasingly compromise berry quality, phenology, and yield. Despite decades of molecular characterization, translating stress biology knowledge into climate-resilient cultivars remains limited. We argue this gap reflects not a lack of knowledge within individual biological layers, but a fundamental failure to integrate across them. Grapevine stress tolerance operates through three interconnected regulatory layers. Transcription factor networks, WRKY, NAC, MYB, DREB, and bZIP families, constitute the most rapid layer, converging on shared ABA-mediated signaling hubs despite apparent stress-type specificity. Quantitative trait loci and genome-wide association studies capture the genomic architecture underlying these responses, yet remain critically under characterized for drought, salinity, and heavy metal tolerance. Epigenetic regulation through DNA methylation, histone modifications, and stress memory mechanisms constitutes a temporally durable third layer, uniquely important for perennial crops where adaptive chromatin states persist across growing seasons. Critically, these layers are not independent: transcription factor activity shapes the chromatin landscape, epigenetic marks modulate QTL expression, and genomic loci encode the regulatory machinery executing stress responses. Current breeding tools, marker-assisted selection, CRISPR/Cas9, and epigenomic selection, map onto these three layers but are overwhelmingly applied in isolation, limiting their collective impact. This review synthesizes knowledge gaps across all three layers within a unified hierarchical framework, arguing that deliberate cross-layer integration through multi-omics and precision breeding could enable cultivars capable of sustaining productivity under a rapidly changing climate.

Hamza Ali, Rahmatullah Khan, Lu Bian et al. · 0 citations
Jul 2026

The fungal effector CvA10999 suppresses plant immunity by targeting VvSnRKb1 to facilitate Colletotrichum viniferum virulence.

Colletotrichum viniferum, the causal agent of grape ripe rot and leaf spot, poses a serious threat to grape yield and fruit quality. Like many phytopathogens, C. viniferum secretes effector proteins; however, the molecular mechanisms by which these effectors manipulate host immune responses remain poorly understood. In this study, we functionally characterized a candidate effector, CvA10999. CvA10999 suppressed INF1 (infestans 1, P. infestans PAMP elicitor) triggered cell death in Nicotiana benthamiana and was significantly upregulated during C. viniferum infection of susceptible grape V. vinifera cv. Thompson Seedless (TS) leaves. Targeted deletion of CvA10999 resulted in reduced sporulation, abnormal appressorium formation, and attenuated virulence on TS leaves. Further analysis revealed that CvA10999 interacts with the grape protein β-subunit of sucrose non-fermenting 1-related protein kinase (VvSnRKb1). Transient overexpression of VvSnRKb1 in TS leaves, as well as stable transgenic grapevines overexpressing VvSnRKb1, conferred enhanced resistance to C. viniferum. Mechanistically, CvA10999 bound to VvSnRKb1, disrupting its interaction with nonexpressor of pathogenesis-related genes 1 (VvNPR1) and interfering with VvNPR1 phosphorylation. This likely impaired the transcriptional activator function of VvNPR1 and downregulated salicylic acid (SA)-responsive pathogenesis-related (PR) genes. Collectively, these findings demonstrate that CvA10999 targets VvSnRKb1 to subvert host immunity and promote C. viniferum infection.

Mengru Dou, Yuhang Li, Zinuo Feng et al. · 0 citations