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A fly model for the CCUG-repeat expansion of myotonic dystrophy type 2 reveals a novel interaction with MBNL1

Expanded non-coding RNA repeats of CUG and CCUG are the underlying genetic causes for myotonic dystrophy type 1 (DM1) and type 2 (DM2), respectively. A gain-of-function of these pathogenic repeat expansions is mediated at least in part by their abnormal interactions with RNA-binding proteins such as...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Yu, Zhenming, Goodman, Lindsey D., Shieh, Shin-Yi, Min, Michelle, Teng, Xiuyin, Zhu, Yongqing, Bonini, Nancy M.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2015
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6281364/
https://ncbi.nlm.nih.gov/pubmed/25305073
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu507
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