This review examines how small RNAs control development in plants, suggesting mechanisms for enhanced precision in their mobility.
Intercellular movement of small RNAs (sRNAs) is fundamental to the growth and survival of plants. Mobile sRNAs function as short- and long-range signals that coordinate developmental patterning, integrate physiological and stress responses, and safeguard reproductive success and genome integrity. Recent advances show that sRNA mobility is not governed simply by plasmodesmata (PD) permeability. Instead, multiple regulatory layers govern which sRNAs become mobile, which cell-cell interfaces they can travers, and where they act. Specialized nuclear export pathways and cytoskeleton-dependent mechanisms enable mobile sRNAs to escape sequestration into cell-autonomous ARGONAUTE proteins. In parallel, gatekeeping factors, potentially localized at PDs, generate selective and directional mobility-particularly in stem-cell niches and the central vasculature-to ensure that mobile sRNAs deliver precise positional information. In this review, we summarize contributions from mobile sRNAs to development and synthesize recent advances in understanding how the mobile sRNA pool is generated, how sRNAs traverse plasmodesmata, and how developmental context shapes mobility. We highlight unresolved questions and emerging concepts that explain how plants impose precision on these central organizers of development and environmental adaptability.
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Herrmann et al. (2026) studied this question.
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