Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cells

Yanovsky-Dagan, S; Mor-Shaked, H; Eiges, R

HERO ID

3044688

Reference Type

Journal Article

Subtype

Review

Year

2015

Language

English

PMID

26131313

HERO ID 3044688
Material Type Review
In Press No
Year 2015
Title Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cells
Authors Yanovsky-Dagan, S; Mor-Shaked, H; Eiges, R
Journal World Journal of Stem Cells
Volume 7
Issue 5
Page Numbers 823-838
Abstract Pathogenic mutations involving DNA repeat expansions are responsible for over 20 different neuronal and neuromuscular diseases. All result from expanded tracts of repetitive DNA sequences (mostly microsatellites) that become unstable beyond a critical length when transmitted across generations. Nearly all are inherited as autosomal dominant conditions and are typically associated with anticipation. Pathologic unstable repeat expansions can be classified according to their length, repeat sequence, gene location and underlying pathologic mechanisms. This review summarizes the current contribution of mutant pluripotent stem cells (diseased human embryonic stem cells and patient-derived induced pluripotent stem cells) to the research of unstable repeat pathologies by focusing on particularly large unstable noncoding expansions. Among this class of disorders are Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome, myotonic dystrophy type 1 and myotonic dystrophy type 2, Friedreich ataxia and C9 related amyotrophic lateral sclerosis and/or frontotemporal dementia, Facioscapulohumeral Muscular Dystrophy and potentially more. Common features that are typical to this subclass of conditions are RNA toxic gain-of-function, epigenetic loss-of-function, toxic repeat-associated non-ATG translation and somatic instability. For each mechanism we summarize the currently available stem cell based models, highlight how they contributed to better understanding of the related mechanism, and discuss how they may be utilized in future investigations.
Doi 10.4252/wjsc.v7.i5.823
Pmid 26131313
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English