| Literature DB >> 33627639 |
Magdalena Derbis1, Emre Kul2, Daria Niewiadomska1, Michał Sekrecki1, Agnieszka Piasecka1, Katarzyna Taylor1, Renate K Hukema3,4, Oliver Stork2, Krzysztof Sobczak5.
Abstract
Fragile X-associated tremor/ataxia syndrome (FXTAS) is an incurable neurodegenerative disorder caused by expansion of CGG repeats in the FMR1 5'UTR. The RNA containing expanded CGG repeats (rCGGexp) causes cell damage by interaction with complementary DNA, forming R-loop structures, sequestration of nuclear proteins involved in RNA metabolism and initiation of translation of polyglycine-containing protein (FMRpolyG), which forms nuclear insoluble inclusions. Here we show the therapeutic potential of short antisense oligonucleotide steric blockers (ASOs) targeting directly the rCGGexp. In nuclei of FXTAS cells ASOs affect R-loop formation and correct miRNA biogenesis and alternative splicing, indicating that nuclear proteins are released from toxic sequestration. In cytoplasm, ASOs significantly decrease the biosynthesis and accumulation of FMRpolyG. Delivery of ASO into a brain of FXTAS mouse model reduces formation of inclusions, improves motor behavior and corrects gene expression profile with marginal signs of toxicity after a few weeks from a treatment.Entities:
Year: 2021 PMID: 33627639 DOI: 10.1038/s41467-021-21021-w
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919