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Status |
Public on Feb 16, 2022 |
Title |
RNA-Seq transcriptome profiling of human iPS cell-derived cardiomyocytes (hiPSC-CMs) following overexpression (OE) of estrogen-related receptor gamma (ERRg) |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Transcriptional regulatory circuits that drive cardiomyocyte maturation are poorly understood. Human iPS cell-derived cardiomyocytes (hiPSC-CMs) have been shown to have fetal cardiomyocyte features in terms of metabolic gene expression profiles. Here we found that in hiPSC-CMs, overexpression of estrogen-related receptor gamma (ERRg) is sufficient to drive cardiomyocyte metabolic maturation programs including the induction of a number of oxidative mitochondrial metabolic genes.
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Overall design |
Examination of how gene expression levels are changed by OE ERRg compared to OE GFP in hiPSC-CMs in triplicate.
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Contributor(s) |
Sakamoto T, Batmanov K, Kelly DP |
Citation(s) |
35418170 |
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Submission date |
Feb 02, 2021 |
Last update date |
May 05, 2022 |
Contact name |
Tomoya Sakamoto |
Organization name |
University of Pennsylvania
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Department |
Cardiovascular Institute
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Lab |
Daniel Kelly lab
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Street address |
Smilow Center for Translational Research 11th FL (Room 11-172) 3400 Civic Center Blvd Bldg 421
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City |
Philadelphia |
State/province |
PA |
ZIP/Postal code |
19104 |
Country |
USA |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE166064 |
The Nuclear Receptor ERR Cooperates with the Cardiogenic Factor GATA4 to Orchestrate Transcriptional Control of Cardiac Maturation |
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Relations |
BioProject |
PRJNA698780 |
SRA |
SRP304240 |