Literature DB >> 27256390

RNA Granules and Diseases: A Case Study of Stress Granules in ALS and FTLD.

Alexander C Fan1, Anthony K L Leung2.   

Abstract

RNA granules are microscopically visible cellular structures that aggregate by protein-protein and protein-RNA interactions. Using stress granules as an example, we discuss the principles of RNA granule formation, which rely on the multivalency of RNA and multi-domain proteins as well as low-affinity interactions between proteins with prion-like/low-complexity domains (e.g. FUS and TDP-43). We then explore how dysregulation of RNA granule formation is linked to neurodegenerative diseases, such as amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD), and discuss possible strategies for therapeutic intervention.

Entities:  

Keywords:  Low-complexity region; Phase separation; Prion-like domain; RNA granules; Stress granules

Mesh:

Substances:

Year:  2016        PMID: 27256390      PMCID: PMC5247449          DOI: 10.1007/978-3-319-29073-7_11

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  165 in total

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Review 3.  Regulation of cytoplasmic mRNA decay.

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Journal:  Mol Cell Biol       Date:  2010-12-20       Impact factor: 4.272

5.  Inhibition of mTORC1 by astrin and stress granules prevents apoptosis in cancer cells.

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Journal:  Cell       Date:  2013-08-15       Impact factor: 41.582

6.  RhoA/ROCK1 signaling regulates stress granule formation and apoptosis.

Authors:  Nien-Pei Tsai; Li-Na Wei
Journal:  Cell Signal       Date:  2009-12-11       Impact factor: 4.315

7.  Translation suppression promotes stress granule formation and cell survival in response to cold shock.

Authors:  Sarah Hofmann; Valeria Cherkasova; Peter Bankhead; Bernd Bukau; Georg Stoecklin
Journal:  Mol Biol Cell       Date:  2012-08-08       Impact factor: 4.138

Review 8.  Regulation of stress granules in virus systems.

Authors:  James P White; Richard E Lloyd
Journal:  Trends Microbiol       Date:  2012-03-07       Impact factor: 17.079

9.  Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models.

Authors:  Maria Armakola; Matthew J Higgins; Matthew D Figley; Sami J Barmada; Emily A Scarborough; Zamia Diaz; Xiaodong Fang; James Shorter; Nevan J Krogan; Steven Finkbeiner; Robert V Farese; Aaron D Gitler
Journal:  Nat Genet       Date:  2012-10-28       Impact factor: 38.330

10.  Autophagy induction enhances TDP43 turnover and survival in neuronal ALS models.

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Journal:  Nat Chem Biol       Date:  2014-06-29       Impact factor: 15.040

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Review 2.  It's Just a Phase: Exploring the Relationship Between mRNA, Biomolecular Condensates, and Translational Control.

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Review 6.  Reimagining dots and dashes: Visualizing structure and function of organelles for high-content imaging analysis.

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Review 7.  Proteostatic imbalance and protein spreading in amyotrophic lateral sclerosis.

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Review 8.  Autophagy Dysregulation in ALS: When Protein Aggregates Get Out of Hand.

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Review 9.  Cellular Chaperones As Therapeutic Targets in ALS to Restore Protein Homeostasis and Improve Cellular Function.

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Review 10.  Protein Phase Separation during Stress Adaptation and Cellular Memory.

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