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Status |
Public on Nov 05, 2020 |
Title |
Transcriptome analysis of the TA muscles from WT and Dmd Exon 51 Knockout mice |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Duchenne muscular dystrophy (DMD) is a fatal muscle disorder characterized by cycles of degeneration and regeneration of multinucleated myofibers and pathological activation of a variety of other associated cell types. Here, we describe the creation of a new mouse model of DMD caused by deletion of exon 51 of the dystrophin gene, which represents a prevalent mutation in humans. To understand the transcriptional abnormalities and heterogeneity associated with the nuclei of myofibers, as well as other mononucleated cell types that contribute to DMD disease pathogenesis, we performed single nucleus transcriptomics of skeletal muscle of mice with exon 51 deletion. Our results reveal distinctive and previously unrecognized myonuclear subtypes within dystrophic myofibers and uncover degenerative and regenerative transcriptional pathways underlying DMD pathogenesis. Our findings provide new insights into the molecular underpinnings of DMD, controlled by the transcriptional activity of different types of muscle and nonmuscle nuclei.
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Overall design |
RNA was isolated from TA muscles of 1 month old WT or DMD ∆Ex51 mice. Stranded mRNA-seq was performed to profile gene expression changes upon exon 51 deletion.
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Contributor(s) |
Chemello F, Wang Z, Olson EN |
Citation(s) |
33148801 |
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Submission date |
Aug 19, 2020 |
Last update date |
Nov 05, 2020 |
Contact name |
Zhaoning Wang |
E-mail(s) |
zhw063@health.ucsd.edu
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Organization name |
UC San Diego
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Department |
Cellular and Molecular Medicine
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Lab |
Bing Ren Lab
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Street address |
9500 Gilman Drive
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City |
La Jolla |
State/province |
California |
ZIP/Postal code |
92093 |
Country |
USA |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE156498 |
Degenerative and Regenerative Pathways Underlying Duchenne Muscular Dystrophy Revealed by Single-nucleus RNA sequencing |
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Relations |
BioProject |
PRJNA658118 |
SRA |
SRP278118 |