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Expanded CUG repeats in DMPK transcripts adopt diverse hairpin conformations without influencing the structure of the flanking sequences

Myotonic dystrophy type 1 (DM1) is a complex neuromuscular disorder caused by expansion of a CTG repeat in the 3′-untranslated region (UTR) of the DMPK gene. Mutant DMPK transcripts form aberrant structures and anomalously associate with RNA-binding proteins (RBPs). As a first step toward better und...

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發表在:RNA
Main Authors: van Cruchten, Remco T.P., Wieringa, Bé, Wansink, Derick G.
格式: Artigo
語言:Inglês
出版: Cold Spring Harbor Laboratory Press 2019
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6426290/
https://ncbi.nlm.nih.gov/pubmed/30700578
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.068940.118
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