Integrating epigenetic memory and plant growth-promoting rhizobacteria-mediated signaling for climate-resilient...

Climate change is shifting agriculture toward multifactorial abiotic stresses (drought, heat, and salinity). This study aims to characterize emergent, non-additive plant responses to combined stresses and to define the epigenetic and microbial frameworks that govern environmental memory and adaptive plasticity.

We conducted a meta-synthesis of molecular and ecological studies, evaluating high-throughput data on DNA methylation, histone modifications, and ncRNA profiles. We further analyzed the plant holobiont to determine how rhizosphere and endosphere microbiota influence host stress imprinting. The analysis revealed that stress combinations trigger distinct transcriptomic and metabolic signatures, which are stabilized by an "epigenetic toolkit" such as RNA-directed DNA methylation and chromatin remodeling. Furthermore, plant-associated microbiota serve as an extrinsic regulatory layer, modulating host epigenetic states to prime plants for compound stress. While translational pathways such as epigenetic editing, Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) mediated epigenome editing, and microbiome engineering show promise, their field-scale stability remains context-dependent.

Building climate resilience requires a paradigm shift from traditional single-trait breeding toward multi-scale regulatory approaches. Harnessing the synergy between the plant epigenome and the microbiome enables the development of 'primed' crop varieties-an integrated strategy vital for safeguarding global food security amid intensifying environmental volatility.