Literature DB >> 30606735

Liquid- and solid-like RNA granules form through specific scaffold proteins and combine into biphasic granules.

Nobuyuki Shiina1,2,3.   

Abstract

RNA granules consist of membrane-less RNA-protein assemblies and contain dynamic liquid-like shells and stable solid-like cores, which are thought to function in numerous processes in mRNA sorting and translational regulation. However, how these distinct substructures are formed, whether they are assembled by different scaffolds, and whether different RNA granule scaffolds induce these different substructures remains unknown. Here, using fluorescence microscopy-based morphological and molecular-dynamics analyses, we demonstrate that RNA granule scaffold proteins (scaffolds) can be largely classified into two groups, liquid and solid types, which induce the formation of liquid-like and solid-like granules, respectively, when expressed separately in cultured cells. We found that when co-expressed, the liquid-type and solid-type scaffolds combine and form liquid- and solid-like substructures in the same granules, respectively. The combination of the different types of scaffolds reduced the immobile fractions of the solid-type scaffolds and their dose-dependent ability to decrease nascent polypeptides in granules, but had little effect on the dynamics of the liquid-type scaffolds or their dose-dependent ability to increase nascent polypeptides in granules. These results suggest that solid- and liquid-type scaffolds form different substructures in RNA granules and differentially affect each other. Our findings provide detailed insight into the assembly mechanism and distinct dynamics and functions of core and shell substructures in RNA granules.
© 2019 Shiina.

Keywords:  RNA binding protein; RNA granule; cell permeabilization; core-shell; fluorescence recovery after photobleaching (FRAP); liquid; liquid–liquid phase separation (LLPS); molecular dynamics; scaffold protein; solid

Mesh:

Substances:

Year:  2019        PMID: 30606735      PMCID: PMC6416441          DOI: 10.1074/jbc.RA118.005423

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


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