Title of article
Cell-free Formation of RNA Granules: Low Complexity Sequence Domains Form Dynamic Fibers within Hydrogels
Author/Authors
Masato Kato، نويسنده , , Tina W. Han، نويسنده , , Shanhai Xie، نويسنده , , Kevin Shi، نويسنده , , Xinlin Du، نويسنده , , Leeju C. Wu، نويسنده , , Hamid Mirzaei، نويسنده , , Elizabeth J. Goldsmith، نويسنده , , Jamie Longgood، نويسنده , , Jimin Pei، نويسنده , , Nick V. Grishin، نويسنده , , Douglas E. Frantz، نويسنده , , Jay W. Schneider، نويسنده , , She Chen، نويسنده , , Lin Li، نويسنده , , Michael R. Sawaya، نويسنده , , David Eisenberg، نويسنده , , Robert Tycko، نويسنده , , Steven L. McKnight، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2012
Pages
15
From page
753
To page
767
Abstract
Eukaryotic cells contain assemblies of RNAs and proteins termed RNA granules. Many proteins within these bodies contain KH or RRM RNA-binding domains as well as low complexity (LC) sequences of unknown function. We discovered that exposure of cell or tissue lysates to a biotinylated isoxazole (b-isox) chemical precipitated hundreds of RNA-binding proteins with significant overlap to the constituents of RNA granules. The LC sequences within these proteins are both necessary and sufficient for b-isox-mediated aggregation, and these domains can undergo a concentration-dependent phase transition to a hydrogel-like state in the absence of the chemical. X-ray diffraction and EM studies revealed the hydrogels to be composed of uniformly polymerized amyloid-like fibers. Unlike pathogenic fibers, the LC sequence-based polymers described here are dynamic and accommodate heterotypic polymerization. These observations offer a framework for understanding the function of LC sequences as well as an organizing principle for cellular structures that are not membrane bound.
Journal title
CELL
Serial Year
2012
Journal title
CELL
Record number
1021176
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