RAN translation at CGG repeats induces ubiquitin proteasome system impairment in models of fragile X-associated tremor ataxia syndrome.

Abstract

Fragile X-associated tremor ataxia syndrome (FXTAS) is a neurodegenerative disorder caused by a CGG trinucleotide repeat expansion in the 5' UTR of the Fragile X gene, FMR1. FXTAS is thought to arise primarily from an RNA gain-of-function toxicity mechanism. However, recent studies demonstrate that the repeat also elicits production of a toxic polyglycine protein, FMRpolyG, via repeat-associated non-AUG (RAN)-initiated translation. Pathologically, FXTAS is characterized by ubiquitin-positive intranuclear neuronal inclusions, raising the possibility that failure of protein quality control pathways could contribute to disease pathogenesis. To test this hypothesis, we used Drosophila- and cell-based models of CGG-repeat-associated toxicity. In Drosophila, ubiquitin proteasome system (UPS) impairment led to enhancement of CGG-repeat-induced degeneration, whereas overexpression of the chaperone protein HSP70 suppressed this toxicity. In transfected mammalian cells, CGG repeat expression triggered accumulation of a UPS reporter in a length-dependent fashion. To delineate the contributions from CGG repeats as RNA from RAN translation-associated toxicity, we enhanced or impaired the production of FMRpolyG in these models. Driving expression of FMRpolyG enhanced induction of UPS impairment in cell models, while prevention of RAN translation attenuated UPS impairment in cells and suppressed the genetic interaction with UPS manipulation in Drosophila. Taken together, these findings suggest that CGG repeats induce UPS impairment at least in part through activation of RAN translation.

• Authors: Seok Yoon Oh, Fang He, Amy Krans, Michelle Frazer, J Paul Taylor, Henry L Paulson, Peter K Todd
• Journal: Human molecular genetics (Hum Mol Genet) Vol. 24 Issue 15 Pg. 4317-26 (Aug 01 2015) ISSN: 1460-2083 [Electronic] England
• PMID: 25954027 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
• Copyright: Published by Oxford University Press 2015. This work is written by (a) US Government employee(s) and is in the public domain in the US.

Chemical References

• Drosophila Proteins
• FMR1 protein, Drosophila
• FMR1 protein, human
• Ubiquitin
• Fragile X Mental Retardation Protein
• Proteasome Endopeptidase Complex

Topics

• Animals
• Animals, Genetically Modified
• Ataxia (genetics, pathology)
• Disease Models, Animal
• Drosophila Proteins (genetics)
• Drosophila melanogaster
• Fragile X Mental Retardation Protein (genetics)
• Fragile X Syndrome (genetics, pathology)
• Humans
• Mice
• Neurodegenerative Diseases
• Proteasome Endopeptidase Complex (genetics, metabolism)
• Tremor (genetics, pathology)
• Trinucleotide Repeat Expansion (genetics)
• Ubiquitin (genetics, metabolism)