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Status |
Public on Jan 31, 2012 |
Title |
Genome-wide analysis of gene expression changes in miR-214 KO mouse hearts and skeletal muscle |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
Early reperfusion of ischemic cardiac tissue remains the most effective intervention for improving clinical outcome following myocardial infarction. However, abrupt increases in intracellular Ca2+ during myocardial reperfusion cause cardiomyocyte death and consequent loss of cardiac function, referred to as ischemia/reperfusion (IR) injury. Cardiac IR is accompanied by dynamic changes in expression of microRNAs (miRNAs), which inhibit specific mRNA targets. miR-214 is up-regulated during ischemic injury and heart failure in mice and humans, but its potential role in these processes is unknown. We show that genetic deletion of miR-214 in mice causes loss of cardiac contractility, increased apoptosis, and excessive fibrosis in response to IR injury.
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Overall design |
The microarray contains 6 samples, each containing cDNA pooled from 3 mice per group. There are no replicates. The array was designed to make 3 different pairwise comparisons between the following: P14 WT and miR-214 KO hearts; adult WT and miR-214 KO skeletal muscle; adult WT and miR-214 KO hearts
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Contributor(s) |
Aurora AB, Olson EN |
Citation(s) |
22426211 |
Submission date |
Jan 30, 2012 |
Last update date |
Sep 23, 2019 |
Contact name |
Arin B Aurora |
E-mail(s) |
arinaurora@gmail.com
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Organization name |
UT Southwestern Medical Center
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Department |
Molecular Biology
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Lab |
Eric N. Olson
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Street address |
6000 Harry Hines Blvd
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City |
Dallas |
State/province |
TX |
ZIP/Postal code |
75235 |
Country |
USA |
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Platforms (1) |
GPL6887 |
Illumina MouseWG-6 v2.0 expression beadchip |
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Samples (6)
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Relations |
BioProject |
PRJNA152583 |