| Literature DB >> 27768897 |
Yi Lin1, Eiichiro Mori1, Masato Kato1, Siheng Xiang1, Leeju Wu1, Ilmin Kwon2, Steven L McKnight3.
Abstract
Two complementary approaches were used in search of the intracellular targets of the toxic PR poly-dipeptide encoded by the repeat sequences expanded in the C9orf72 form of amyotrophic lateral sclerosis. The top categories of PRn-bound proteins include constituents of non-membrane invested cellular organelles and intermediate filaments. PRn targets are enriched for the inclusion of low complexity (LC) sequences. Evidence is presented indicating that LC sequences represent the direct target of PRn binding and that interaction between the PRn poly-dipeptide and LC domains is polymer-dependent. These studies indicate that PRn-mediated toxicity may result from broad impediments to the dynamics of cell structure and information flow from gene to message to protein. Published by Elsevier Inc.Entities:
Keywords: 1,6-hexanediol; C9orf72; amyloid-like polymers; cellular puncta not invested by surrounding membranes; intermediate filaments; labile; low complexity sequence polymers; toxic PRn and GRn poly-dipeptides
Mesh:
Substances:
Year: 2016 PMID: 27768897 PMCID: PMC5076566 DOI: 10.1016/j.cell.2016.10.003
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582