RNA interference targeting CUG repeats in a mouse model of myotonic dystrophy

Mol Ther. 2013 Feb;21(2):380-7. doi: 10.1038/mt.2012.222. Epub 2012 Nov 27.

Abstract

Myotonic dystrophy type 1 (DM1) is an RNA dominant disease caused by expression of DM protein kinase (DMPK) transcripts that contain an expanded CUG repeat (CUG(exp)). The toxic mRNA localizes to nuclear foci and sequesters proteins involved in the regulation of alternative splicing, such as, muscleblind-like 1 (MBNL1). Here, we used synthetic short interfering RNAs (siRNAs) to target CUG repeats and test the concept that inhibiting the expression of CUG(exp) RNA can mitigate features of DM1 in transgenic mice. Intramuscular injection and electroporation of siRNA resulted in ~70-80% downregulation of CUG(exp) transcripts. A limited survey of endogenous mouse transcripts that contain nonexpanded CUG or CAG repeats showed that most were not affected, though Txlnb containing (CUG)(9) was significantly reduced. By this strategy, the number and intensity of CUG(exp) nuclear foci were reduced and splicing of MBNL1-dependent exons was improved. These data suggest that the expanded CUG repeats are a potential target for allele-selective RNA interference.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing / genetics
  • Amino Acid Sequence
  • Animals
  • Cell Line, Tumor
  • Cell Nucleus / chemistry
  • Cell Nucleus / genetics
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Disease Models, Animal
  • Electromyography
  • Exons
  • Fluorescent Antibody Technique
  • Humans
  • In Situ Hybridization, Fluorescence
  • Mice
  • Mice, Transgenic
  • Microscopy, Fluorescence
  • Molecular Sequence Data
  • Myotonic Dystrophy / genetics*
  • Myotonic Dystrophy / pathology
  • Myotonic Dystrophy / therapy*
  • Myotonin-Protein Kinase
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • RNA Interference*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism
  • Trinucleotide Repeat Expansion*

Substances

  • DMPK protein, human
  • DMPK protein, mouse
  • DNA-Binding Proteins
  • Mbnl1 protein, mouse
  • RNA, Messenger
  • RNA, Small Interfering
  • RNA-Binding Proteins
  • Myotonin-Protein Kinase
  • Protein Serine-Threonine Kinases