Phosphite (Phi) and phosphate (Pi) share the same root uptake system, but Phi acts as a biostimulant that modulates plant growth and disease resistance in a species‑ and Pi‑dependent manner. In Arabidopsis, Phi induces hypersensitive‑like cell death and enhances resistance to Plectosphaerella cucumerina, while in rice it counteracts Pi‑induced susceptibility to Magnaporthe oryzae and Fusarium fujikuroi, accompanied by extensive transcriptional reprogramming.

The authors used a bottom‑up thermodynamic modelling framework to investigate how plants decode calcium signals, starting from Ca2+ binding to EF‑hand proteins and extending to higher‑order decoding modules. They identified six universal Ca2+-decoding modules that can explain variations in calcium sensitivity among kinases and provide a theoretical basis for interpreting calcium signal amplitude and frequency in plant cells.

The study uncovers a reciprocal regulatory loop between type one protein phosphatases (TOPPs) and EIN2 in ethylene signaling, showing that ethylene induces TOPPs expression and that TOPPs dephosphorylate EIN2 at S655 to stabilize it and promote nuclear accumulation. TOPPs act upstream of EIN2, while EIN3/EIL1 transcriptionally activates TOPPs, linking dephosphorylation to enhanced ethylene responses and improved salt tolerance.

The study examines how the SnRK1 catalytic subunit KIN10 integrates carbon availability with root growth regulation in Arabidopsis thaliana. Loss of KIN10 reduces glucose‑induced inhibition of root elongation and triggers widespread transcriptional reprogramming of metabolic and hormonal pathways, notably affecting auxin and jasmonate signaling under sucrose supplementation. These findings highlight KIN10 as a central hub linking energy status to developmental and environmental cues in roots.

The study compared physiological, ion‑balance, and metabolic responses of two maize inbred lines—salt‑sensitive C68 and salt‑tolerant NC326—under salinity stress. Untargeted metabolomics identified 56 metabolites and, together with genetic analysis, linked 10 candidate genes to key protective metabolites, revealing constitutive and inducible mechanisms of salt tolerance.

The study produced a chromosome-level genome assembly (544.7 Mb) for the wild rose Rosa lucieae and identified gene duplications and rapidly evolving stress‑response gene families likely underpinning its salt tolerance. Comparative analyses highlighted recent duplications and divergence of genes involved in stress signaling, homeostasis, and detoxification, providing a genomic resource for rose breeding.