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Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS
- Ravenscroft, Thomas A;
- Baker, Matt C;
- Rutherford, Nicola J;
- Neumann, Manuela;
- Mackenzie, Ian R;
- Josephs, Keith A;
- Boeve, Bradley F;
- Petersen, Ronald;
- Halliday, Glenda M;
- Kril, Jillian;
- van Swieten, John C;
- Seeley, William W;
- Dickson, Dennis W;
- Rademakers, Rosa
Published Web Location
https://doi.org/10.1016/j.neurobiolaging.2013.04.004Abstract
The nuclear protein fused in sarcoma (FUS) is found in cytoplasmic inclusions in a subset of patients with the neurodegenerative disorder frontotemporal lobar degeneration (FTLD-FUS). FUS contains a methylated arginine-glycine-glycine domain that is required for transport into the nucleus. Recent findings have shown that this domain is hypomethylated in patients with FTLD-FUS. To determine whether the cause of hypomethylation is the result of mutations in protein N-arginine methyltransferases (PRMTs), we selected 3 candidate genes (PRMT1, PRMT3, and PRMT8) and performed complete sequencing analysis and real-time polymerase chain reaction mRNA expression analysis in 20 FTLD-FUS cases. No mutations or statistically significant changes in expression were observed in our patient samples, suggesting that defects in PRMTs are not the cause of FTLD-FUS.
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