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 ,
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.