Spinocerebellar ataxia type 10 (SCA10), an autosomal dominant cerebellar ataxia, is caused by a large expansion mutation of intronic ATTCT pentanucleotide repeat in the ATXN10 gene. Our studies have suggested that toxic RNA rather than altered function of the protein product of ATXN10 is the likely cause of SCA10. We showed that the untranslated RNA transcript of the expanded repeat is accumulated in intracellular foci and interacts with heterogeneous nuclear ribonucleoprotein K (hnRNP K). Preliminary data from cell culture and transgenic mouse models suggested that expression of (AUUCU) 500 repeats causes deleterious downstream events similar to those seen in cells and a brain of SCA10 patient. Knockdown of hnRNP K recapitulates some of these events in cell culture. The goal of this application is to demonstrate that the sequestration of hnRNP K plays a key role in SCA10 pathogenesis and to determine the relative contribution of this mechanism to the entire pathogenicity in SCA10. Our central hypothesis is that the major pathogenic mechanism of SCA10 is an RNA gain-of-function that causes functional loss of hnRNP K. To examine this hypothesis we propose: ? Aim 1: Demonstrate binding of the expanded AUUCU repeat RNA to hnRNP K. We will perform unbiased searches of interacting proteins by pull-down/mass spectroscopy studies and in-silico bioinformatics, followed by co-immunoprecipitation, electromobility shift assay and high-throughput crosslinking studies. ? Aim 2: Obtain evidence that hnRNP K sequestration causes neuronal dysfunction and cell death. We will recapitulate downstream changes found in the SCA10 brain and SCA10 models, such as activation of apoptotic pathways and abnormal alternative splicing of a variety of transcripts, by knockdown of hnRNP K in wild-type mice and cell cultures including neural cells derived from induced pluripotent stem (iPS) cells. ? Aim 3: Determine the relative contribution of hnRNP K to the SCA10 pathogenicity by examining the degree of rescue achieved by over-expression of hnRNP K in cell culture and transgenic mouse models. These studies will firmly establish the pathogenic role of hnRNP K and provide a therapeutic target.

Public Health Relevance

SCA10 is a rare but one of the prototypes of disorders caused by toxic RNA. Toxic RNA is an emerging theme in a variety of disorders. This study will focus on hnRNP K, a protein with multiple essential functions for viability of cells and an interest to a wie variety of biomedical researchers. Our data on functional deficiency of hnRNP K will be important for understanding the mechanism of SCA10 and other disorders.

National Institute of Health (NIH)
National Institute of Neurological Disorders and Stroke (NINDS)
Research Project (R01)
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Cell Death in Neurodegeneration Study Section (CDIN)
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Gwinn, Katrina
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Methodist Hospital Research Institute
United States
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Moscovich, Mariana; Munhoz, Renato Puppi; Moro, Adriana et al. (2018) Olfactory Function in SCA10. Cerebellum :
Ashizawa, Ana Tari; Holt, Jenny; Faust, Kelsey et al. (2018) Intravenously Administered Novel Liposomes, DCL64, Deliver Oligonucleotides to Cerebellar Purkinje Cells. Cerebellum :
Sznajder, ?ukasz J; Thomas, James D; Carrell, Ellie M et al. (2018) Intron retention induced by microsatellite expansions as a disease biomarker. Proc Natl Acad Sci U S A 115:4234-4239
Zhang, Linwei; McFarland, Karen N; Subramony, S H et al. (2017) SPG7 and Impaired Emotional Communication. Cerebellum 16:595-598
Schüle, Birgitt; McFarland, Karen N; Lee, Kelsey et al. (2017) Parkinson's disease associated with pure ATXN10 repeat expansion. NPJ Parkinsons Dis 3:27
Zhang, Nan; Ashizawa, Tetsuo (2017) RNA toxicity and foci formation in microsatellite expansion diseases. Curr Opin Genet Dev 44:17-29
Moro, Adriana; Munhoz, Renato P; Moscovich, Mariana et al. (2017) Nonmotor Symptoms in Patients with Spinocerebellar Ataxia Type 10. Cerebellum 16:938-944
Ashizawa, Tetsuo; Xia, Guangbin (2016) Ataxia. Continuum (Minneap Minn) 22:1208-26
Teive, Hélio A G; Ashizawa, Tetsuo (2015) Primary and secondary ataxias. Curr Opin Neurol 28:413-22
Teive, Hélio A G; Moro, Adriana; Moscovich, Mariana et al. (2015) Ataxia-telangiectasia - A historical review and a proposal for a new designation: ATM syndrome. J Neurol Sci 355:3-6

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