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- W2040866074 endingPage "14" @default.
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- W2040866074 abstract "A novel RNA-mediated disease mechanism has emerged from studies on dominantly inherited neurological disorders caused by unstable microsatellite expansions in non-coding regions of the genome. These non-coding tandem repeat expansions trigger the production of unusual RNAs that gain a toxic function, which involves the formation of RNA repeat structures that interact with, and alter the activities of, various factors required for normal RNA processing as well as additional cellular functions. In this review, we explore the deleterious effects of toxic RNA expression and discuss the various model systems currently available for studying RNA gain-of-function in neurologic diseases. Common themes, including bidirectional transcription and repeat-associated non-ATG (RAN) translation, have recently emerged from expansion disease studies. These and other discoveries have highlighted the need for further investigations designed to provide the additional mechanistic insights essential for future therapeutic development. This article is part of a Special Issue entitled RNA Metabolism 2013." @default.
- W2040866074 created "2016-06-24" @default.
- W2040866074 creator A5014465543 @default.
- W2040866074 creator A5036192439 @default.
- W2040866074 creator A5050025082 @default.
- W2040866074 date "2014-10-01" @default.
- W2040866074 modified "2023-10-17" @default.
- W2040866074 title "RNA–protein interactions in unstable microsatellite diseases" @default.
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