Yansong Miao

The gradual assembly and oligomerization of cell surface receptors are critical for regulating immune activation and turnover. Yet, how dynamic, spatiotemporally regulated assembly enables rapid and sustained signaling in plant innate immunity remains unclear, owing to the inherent complexity of their dynamic associations. Using a synthetic engineering approach, we precisely controlled the oligomerization states of the Arabidopsis FLS2 receptor. Single-particle imaging with quantitative calibration revealed that FLS2 transits from a predominantly monomeric resting state to transient homo-association at dimeric configuration upon activation. We then showed that synthetically engineered receptor homo-dimeric association markedly enhances plant defense responses while avoids dysfunctional high-order assemblies, which inhibit dynamic receptor replenishment and thus defect in long-lasting immune activities. Our findings highlight precise receptor assembly control for both immediate activation and long-term signaling, offering strategies for engineering durable plant immune responses.

Biomolecular condensates formed through phase separation have emerged as a central principle of cellular organization, enabling the dynamic regulation of gene expression, signaling, metabolism, and stress responses. While early conceptual advances in condensate biology have largely originated from animal and in vitro systems, plant cells present a unique set of biological and technical challenges, including rigid cell walls, turgor pressure, plastid autofluorescence, complex endomembrane organization, and acute environmental responsiveness. These distinctive features impede the direct transfer of existing methodologies and drive the development of heterogeneous experimental practices. In this community comment, we present a comprehensive methodological framework for studying biomolecular condensates in plants, spanning in silico prediction, in vitro reconstitution, molecular dynamics simulations, live-cell and super-resolution imaging, material property measurements, membrane-associated condensates, and synthetic condensate engineering. We highlight best practices, common pitfalls, and plant-specific considerations, emphasizing the need for orthogonal validation, quantitative interpretation, and physiological relevance. By consolidating current methodologies and articulating shared principles, this review aims to establish a foundation for rigorous, reproducible, and conceptually coherent research in condensate biology of plants and beyond, with emerging implications for crop genetic improvement and synthetic biology applications.

Biomolecular condensates have emerged as versatile regulators of plant cellular processes, offering a dynamic and reversible mechanism to coordinate development, stress response, and spatial organization. Through phase separation, these condensates spatially and temporally modulate biochemical reactions, sequester or activate specific proteins and RNAs, and reshape cellular architecture. This review presents a comprehensive and multidimensional framework for understanding biomolecular condensates in plant biology, from their biophysical properties and ensemble dynamics to their roles across diverse cellular compartments, including plasma membranes, cytoskeleton, intracellular compartments, and chromatin. We highlight their functions in growth, environmental sensing, and defense and discuss current challenges in studying their composition, material properties, and context-dependent behaviors. Understanding plant condensates not only deepens our knowledge of plant cell organization and adaptability but also opens new avenues for biotechnological innovation in agriculture.

Transcriptional condensates formed by MYB-TPL play key roles in fine-tuning seed oil biosynthesis.

Bacterial quorum sensing (QS) signals an increasing threat during pathogenesis. How plants deploy timely defenses through QS perception is poorly understood. Here, we report that Arabidopsis thaliana perceives 2’-aminoacetophenone (2’-AA), a volatile QS signal from Pseudomonas aeruginosa , and mounts a multilayered defense. This response comprises BRI1-ASSOCIATED RECEPTOR KINASE 1 (BAK1)-dependent intracellular immunity, extracellular quorum quenching through the release of acetic acid, and ecological remodeling of the root microbiome to suppress Pseudomonas . Our findings demonstrate that plants can translate the detection of a specific bacterial QS molecule into a coordinated, preemptive disease resistance strategy.

The actin cytoskeleton forms a dynamic network composed of filaments that remain flexible when bundled up, leading to complex filamentous structures in plant cells. Understanding the properties of these filamentous structures under different conditions and in different cell types can provide insight into their function. Yet, despite developments in the study of the plant actin cytoskeleton, it remains challenging to segment and identify actin filamentous structures, preventing quantification of their spatiotemporal properties. To address this problem, we devised a network-based approach termed Graph of Filaments over Time (GraFT) to trace and track filamentous structures in cytoskeleton networks extracted from two-dimensional time series imaging data. Our comparative analyses using both synthetic test cases and real-world actin cytoskeleton networks of Arabidopsis thaliana hypocotyls exposed to different treatments demonstrated that GraFT accurately traces and tracks actin filamentous structures. Moreover, GraFT facilitates automated quantification of properties for filamentous structures, providing fine-grained insights of effects of different treatments on the level of individual structures. Therefore, GraFT offers a substantial step toward an automated framework facilitating robust spatiotemporal studies of the plant actin cytoskeleton.

Electrophysiological signals provide valuable insights into plant health, facilitating measures to enhance crop productivity. Despite advances in measurement methods, long-term (>1 day) acquisition techniques remain limited, hindering continuous monitoring. Current long-term techniques rely on invasive electrodes, as noninvasive electrodes fall short in operational duration and conformability. Here, a capacitively coupled electrode with an adaptable coupling layer is developed for noninvasive, month-long electrophysiological monitoring on diverse plants. The adaptable coupling layer is formed by in situ sol-gel transition, followed by dehydration of thermoresponsive hydrogel on plants, achieving high conformability to complex surfaces and stable electrical coupling. For 1 month on trichome-covered plant surfaces, the electrode maintains a high signal-to-noise ratio comparable to a gold-standard noninvasive electrode, which typically lasts a few hours. Long-term monitoring reveals drought-specific signal features that correlate with plant water status. Physiological investigations indicate an essential role of calcium and reactive oxygen species, highlighting the potential of our electrode in generating biological insights and inspiring plant sensing innovations.