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Elife. 2015 Dec 9;4:e08881. doi: 10.7554/eLife.08881.

GGGGCC microsatellite RNA is neuritically localized, induces branching defects, and perturbs transport granule function.

Author information

1
Department of Biology, University of Pennsylvania, Philadelphia, United States.
2
Department of Neurology, University of Massachusetts Medical School, Worcester, United States.
3
Division of Neurology, Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, United States.
4
Department of Biology, Drexel University, Philadelphia, United States.

Abstract

Microsatellite expansions are the leading cause of numerous neurodegenerative disorders. Here we demonstrate that GGGGCC and CAG microsatellite repeat RNAs associated with C9orf72 in amyotrophic lateral sclerosis/frontotemporal dementia and with polyglutamine diseases, respectively, localize to neuritic granules that undergo active transport into distal neuritic segments. In cultured mammalian spinal cord neurons, the presence of neuritic GGGGCC repeat RNA correlates with neuronal branching defects, and the repeat RNA localizes to granules that label with fragile X mental retardation protein (FMRP), a transport granule component. Using a Drosophila GGGGCC expansion disease model, we characterize dendritic branching defects that are modulated by FMRP and Orb2. The human orthologs of these modifiers are misregulated in induced pluripotent stem cell-differentiated neurons (iPSNs) from GGGGCC expansion carriers. These data suggest that expanded repeat RNAs interact with the messenger RNA transport and translation machinery, causing transport granule dysfunction. This could be a novel mechanism contributing to the neuronal defects associated with C9orf72 and other microsatellite expansion diseases.

KEYWORDS:

ALS; D. melanogaster; FMRP; FTD; GGGGCC; c9orf72; cell biology; spinal cord neurons

PMID:
26650351
PMCID:
PMC4758954
DOI:
10.7554/eLife.08881
[Indexed for MEDLINE]
Free PMC Article

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