4.8 Review

Altered Ribostasis: RNA-Protein Granules in Degenerative Disorders

Journal

CELL
Volume 154, Issue 4, Pages 727-736

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2013.07.038

Keywords

-

Funding

  1. Science Foundation Ireland
  2. Target ALS Foundation
  3. US NIH [NS053825, GM045443]
  4. HHMI

Ask authors/readers for more resources

The molecular processes that contribute to degenerative diseases are not well understood. Recent observations suggest that some degenerative diseases are promoted by the accumulation of nuclear or cytoplasmic RNA-protein (RNP) aggregates, which can be related to endogenous RNP granules. RNP aggregates arise commonly in degenerative diseases because RNA-binding proteins commonly self-assemble, in part through prion-like domains, which can form self-propagating amyloids. RNP aggregates may be toxic due to multiple perturbations of posttranscriptional control, thereby disrupting the normal ribostasis of the cell. This suggests that understanding and modulating RNP assembly or clearance may be effective approaches to developing therapies for these diseases.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available