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May 2, 20264 citations

Programmable artificial RNA condensates in mammalian cells.

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SLShiyi LiYKYuna KimKWKevin Wang

Key Points

  • To develop a method for creating artificial RNA condensates within living mammalian cells to control cellular behavior.
  • Design of modular RNA motifs composed of a single RNA strand.
  • Optimization of RNA sequences for distinct condensate populations and localization control.
  • Integration of RNA linkers to create multi-subcompartment condensates.
  • Artificial RNA condensates formed in the nucleus and cytoplasm through spontaneous self-assembly.
  • Distinct non-mixing condensate populations achieved through sequence optimization.
  • Programmable recruitment of molecules to RNA-rich phases demonstrated.

Abstract

Artificial biomolecular condensates have emerged as powerful tools for controlling cellular behaviour. Here we introduce a method to build artificial condensates within living mammalian cells by designing modular RNA motifs composed of a single short RNA strand. These condensates emerge spontaneously, creating RNA-rich compartments that remain separated from their surrounding environment. The RNA sequences include stem-loop domains that fold as the RNA is transcribed, and then condense in the nucleus and cytoplasm through loop-loop interactions. These sequences can be optimized and diversified, enabling the generation of distinct, non-mixing condensate populations and the programmable control of their subcellular localization. The RNA motifs can also be modified to recruit small molecules, proteins and RNA molecules in a sequence-specific manner to the RNA-rich phase. By introducing RNA linkers, we can build condensates with multiple subcompartments, whose organization can be controlled by tuning the linker stoichiometry. These artificial condensates provide a versatile platform for studying and manipulating molecular functions inside living cells.

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Cite This Study

Li et al. (2026) studied this question.

synapsesocial.com/papers/69f5951171405d493a00002fhttps://doi.org/10.1038/s41565-026-02164-7
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