| Literature DB >> 22579281 |
Masato Kato1, Tina W Han, Shanhai Xie, Kevin Shi, Xinlin Du, Leeju C Wu, Hamid Mirzaei, Elizabeth J Goldsmith, Jamie Longgood, Jimin Pei, Nick V Grishin, Douglas E Frantz, Jay W Schneider, She Chen, Lin Li, Michael R Sawaya, David Eisenberg, Robert Tycko, Steven L McKnight.
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.Entities:
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Year: 2012 PMID: 22579281 PMCID: PMC6347373 DOI: 10.1016/j.cell.2012.04.017
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582