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lüll CAG repeat RNA as an auxiliary toxic agent in polyglutamine disorders Wojciechowska M; Krzyzosiak WJRNA Biol 2011[Jul]; 8 (4): 565-71Over 20 genetic loci with abnormal expansions of short tandem repeats have been associated with human hereditary neurological diseases. Of these, specific trinucleotide repeats located in non-coding and coding regions of individual genes implicated in these disorders are strongly overrepresented. Expansions of CTG, CGG and CAG repeats are linked to, respectively, myotonic dystrophy type 1 (DM1), fragile X-associated tremor/ataxia syndrome (FXTAS), as well as Huntington's disease (HD) and a number of spinocerebellar ataxias (SCAs). Expanded CAG repeats in translated exons trigger the most disorders for which a protein gain-of-function mechanism has been proposed to explain neurodegeneration by polyglutamine-rich (poly-Q) proteins. However, the results of last years showed that RNA composed of mutated CAG repeats can also be toxic and contribute to pathogenesis of polyglutamine disorders through an RNA-mediated gain-of-function mechanism. This mechanism has been best characterized in the non-coding repeat disorder DM1 and is also implicated in several other diseases, such as FXTAS, spinocerebellar ataxia type 8 (SCA8), Huntington's disease-like 2 (HDL2), as well as in myotonic dystrophy type 2 (DM2), spinocerebellar ataxia type 10 (SCA10) and type 31 (SCA31). In this review, we summarize recent findings that emphasize the participation of coding mutant CAG repeat RNA in the pathogenesis of polyglutamine disorders, and we discuss the basis of an RNA gain-of-function model in non-coding diseases such as DM1, FXTAS and SCA8.|*Peptides[MESH]|*Trinucleotide Repeats[MESH]|Fragile X Syndrome/genetics/pathology/physiopathology[MESH]|Heredodegenerative Disorders, Nervous System/*genetics/pathology/physiopathology[MESH]|Humans[MESH]|Myotonic Dystrophy/genetics/pathology/physiopathology[MESH]|RNA/*genetics/metabolism[MESH]|Spinocerebellar Ataxias/genetics/pathology/physiopathology[MESH]|Trinucleotide Repeat Expansion/*genetics[MESH] |