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In vivo discovery of a peptide that prevents CUG–RNA hairpin formation and reverses RNA toxicity in myotonic dystrophy models

Myotonic dystrophy type 1 (DM1) is caused by the expansion of noncoding CTG repeats in the dystrophia myotonica-protein kinase gene. Mutant transcripts form CUG hairpins that sequester RNA-binding factors into nuclear foci, including Muscleblind-like-1 protein (MBNL1), which regulate alternative spl...

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Detalhes bibliográficos
Main Authors: García-López, Amparo, Llamusí, Beatriz, Orzáez, Mar, Pérez-Payá, Enrique, Artero, Ruben D.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3141925/
https://ncbi.nlm.nih.gov/pubmed/21730182
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1018213108
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