Abstract

Liquid–liquid phase separation is thought to be a key organizing principle in eukaryotic cells to generate highly concentrated dynamic assemblies, such as the RNP granules. Numerous in vitro approaches have validated this model, yet a missing aspect is to take into consideration the complex molecular mixture and promiscuous interactions found in vivo. Here we report the versatile scaffold ArtiG to generate concentration-dependent RNA–protein condensates within living cells, as a bottom-up approach to study the impact of co-segregated endogenous components on phase separation. We demonstrate that intracellular RNA seeds the nucleation of the condensates, as it provides molecular cues to locally coordinate the formation of endogenous high-order RNP assemblies. Interestingly, the co-segregation of intracellular components ultimately impacts the size of the phase-separated condensates. Thus, RNA arises as an architectural element that can influence the composition and the morphological outcome of the condensate phases in an intracellular context.

Highlights

  • Liquid–liquid phase separation is thought to be a key organizing principle in eukaryotic cells to generate highly concentrated dynamic assemblies, such as the RNP granules

  • The formation of RNA–protein condensates is thought to be driven by liquid–liquid phase separation through weak, multivalent interactions between biomolecules[8]

  • The Fm protein is a point mutant of human FK506-binding protein (FKBP) protein that has the property of forming homodimers with micromolar affinity[26]

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Summary

Introduction

Liquid–liquid phase separation is thought to be a key organizing principle in eukaryotic cells to generate highly concentrated dynamic assemblies, such as the RNP granules. Ribonucleoprotein (RNP) granules, which include processing bodies (P-bodies), stress granules (SGs), germ granules, nucleoli, Cajal bodies, etc., are supramolecular assemblies of RNA molecules and proteins found in eukaryotic cells[1]. RNA appears to determine the specificity of the molecular composition of the granules as shown for polyQ-dependent RNA–protein assemblies[24] In this context, the development of generic methods, integrating the knowledge accumulated from phase separation in vitro studies, would be acute to elucidate the general principles of the structuring role of RNA within a condensed phase in the cellular environment

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