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Status |
Public on Jun 28, 2012 |
Title |
Antisense oligonucleotides targeting nuclear RNA for in vivo correction of myotonic dystrophy |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
This study examined the effects of antisense oligonucleotides (ASOs) on the muscle transcriptome in a transgenic mouse model of myotonic dystrophy. Two ASOs were tested in HSALR transgenic mice. Both of the ASOs targeted mRNA from a human skeletal actin (hACTA1) transgene. This transgene contains an expanded CTG repeat in the 3’ untranslated region (UTR) (Mankodi et al “Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat” Science 2000; 289:1769-72). ASO 445235 targeted the hACTA1 transcript in the 3’ UTR, downstream from the expanded repeat. ASO 190401 targeted the hACTA1 transcript in the coding region. The HSALR mice received 4 weeks of biweekly subcutaneous injections of vehicle (saline), ASO 190401, or ASO 445236 (n = 4 per group), at a dose of 25 mg/kg per injection. Wild-type mice of the same strain background received saline injections (n = 4). One week after the final injection, quadriceps muscle was harvested for RNA analysis.
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Overall design |
Four conditions, four arrays per condition, to compare WT and HSALR trangenic mice without treatment (saline) and to examine the effect of two oligos (vs. saline) in the HSALR transgenic mice.
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Contributor(s) |
Thornton CA |
Citation(s) |
22859208 |
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Submission date |
Jun 27, 2012 |
Last update date |
Jun 14, 2018 |
Contact name |
Stephen Welle |
E-mail(s) |
[email protected]
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Organization name |
University of Rochester
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Street address |
601 Elmwood Avenue
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City |
Rochester |
State/province |
NY |
ZIP/Postal code |
14642 |
Country |
USA |
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Platforms (1) |
GPL6885 |
Illumina MouseRef-8 v2.0 expression beadchip |
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Samples (16)
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Relations |
BioProject |
PRJNA169527 |