Details:

Alternative Title:
Mol Cell
Publisher's site:
http://dx.doi.org/10.1016/j.molcel.2015.09.017
Personal Author:
Zhang, Huaiying; Elbaum-Garfinkle, Shana; Langdon, Erin; Taylor, Nicole; Occhipinti, Patricia; ... More +
Zhang, Huaiying; Elbaum-Garfinkle, Shana; Langdon, Erin; Taylor, Nicole; Occhipinti, Patricia; Bridges, Andrew; Brangwynne, Clifford P.; Gladfelter, Amy S.; Less -
Description:
Compartmentalization in cells is central to the spatial and temporal control of biochemistry. In addition to membrane-bound organelles, membrane-less compartments form partitions in cells. Increasing evidence suggests that these compartments assemble through liquid-liquid phase separation. However, the spatiotemporal control of their assembly, and how they maintain distinct functional and physical identities, is poorly understood. We have previously shown an RNA-binding protein with a polyQ-expansion called Whi3 is essential for the spatial patterning of cyclin and formin transcripts in cytosol. Here, we show that specific mRNAs that are known physiological targets of Whi3 drive phase separation. mRNA can alter the viscosity of droplets, their propensity to fuse, and the exchange rates of components with bulk solution. Different mRNAs impart distinct biophysical properties of droplets, indicating mRNA can bring individuality to assemblies. Our findings suggest that mRNAs can encode not only genetic information but also the biophysical properties of phase-separated compartments.
Subject:
[+]
Article
Cell Compartmentation
Cyclins
Escherichia Coli
Fungal Proteins
Gene Expression
Gene Expression Regulation, Fungal
Microfilament Proteins
Organelles
Peptides
Phase Transition
Recombinant Fusion Proteins
Rheology
RNA, Fungal
RNA, Messenger
RNA-Binding Proteins
Saccharomycetales

Source:
Mol Cell. 60(2):220-230.;
Pubmed ID:
26474065
Pubmed Central ID:
PMC5221516
Document Type:
Journal Article;
Funding:
R01-GM081506/GM/NIGMS NIH HHS/United States; DP2 GM105437/GM/NIGMS NIH HHS/United States; P30 CA023108/CA/NCI NIH HHS/United States; 1DP2GM105437-01/DP/NCCDPHP CDC HHS/United States; R01 GM081506/GM/NIGMS NIH HHS/United States;
R01-GM081506/GM/NIGMS NIH HHS/United States; DP2 GM105437/GM/NIGMS NIH HHS/United States; P30 CA023108/CA/NCI NIH HHS/United States; 1DP2GM105437-01/DP/NCCDPHP CDC HHS/United States; R01 GM081506/GM/NIGMS NIH HHS/United States; Less -
Collection(s):
CDC Public Access
Main Document Checksum:
[+]
urn:sha256:4f2f0014478e026ba6d4ce757ffe8c6e83a30d859f964f86b2692f5204508eba
File Type:

Supporting Files

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