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Series GSE164061 Query DataSets for GSE164061
Status Public on Oct 11, 2022
Title Lamin A/C-dependent chromatin architecture safeguards naïve pluripotency to prevent aberrant cardiovascular cell fate and function[RNA-seq_ESC]
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Tight control of cell fate choices is crucial for normal development. Here we show that lamin A/C plays a key role in chromatin organization in embryonic stem cells (ESCs), which safeguards naïve pluripotency and ensures proper cell fate choices during cardiogenesis. We find major changes in chromatin compaction and localization of cardiac genes already in Lmna−/−ESCs resulting in precocious activation of a transcriptional program promoting cardiomyocyte versus endothelial cell fate, accompanied by premature cardiomyocyte differentiation, cell cycle withdrawal, and abnormal contractility. Gata4 is activated by lamin A/C loss and Gata4 silencing or haploinsufficiency rescues the aberrant cardiovascular cell fate choices induced by lamin A/C deficiency. Importantly, we observe divergent functions of lamin A/C in naïve pluripotent stem cells and cardiomyocytes, which has distinct contributions to the transcriptional alterations of patients with LMNA-associated cardiomyopathy. Thus, disruption of lamin A/C-dependent chromatin architecture in ESCs is a primary event in LMNA loss-of-function cardiomyopathy.
 
Overall design Conrol and Lmna KO E14 Tg(Nkx2-5-EmGFP) mESCs were maintained on mitomycin treated mouse embryonic fibroblasts (MEF) in DMEM high glucose supplemented with 15% fetal bovine serum, 2 mM L-glutamine, 0.1 mM 2-mercaptoethanol, 0.1 mM non-essential amino acids, 1 mM sodium pyruvate, 4.5 mg/ml D-glucose, 1% penicillin-streptomycin and 1000 U/ml leukemia inhibitory factor and collected for RNA-seq.
 
Contributor(s) Wang Y, Cordero J, Elsherbiny A, Kessler L, Dobreva G
Citation(s) 36333314
Submission date Dec 30, 2020
Last update date Jan 10, 2023
Contact name Gergana Dobreva
E-mail(s) [email protected]
Organization name Medical Faculty Mannheim/University of Heidelberg
Department Cardiovascular Genomics and Epigenomics
Lab AG Dobreva
Street address Ludolf-Krehl-Str. 7-11
City Mannheim
State/province Baden Württemberg
ZIP/Postal code 68167
Country Germany
 
Platforms (1)
GPL23479 BGISEQ-500 (Mus musculus)
Samples (6)
GSM4995991 ESC_LMNA_ctr_RNA_seq_Rep1
GSM4995992 ESC_LMNA_ctr_RNA_seq_Rep2
GSM4995993 ESC_LMNA_ctr_RNA_seq_Rep3
This SubSeries is part of SuperSeries:
GSE164069 Lamin A/C-dependent chromatin architecture safeguards naïve pluripotency to prevent aberrant cardiovascular cell fate and function
Relations
BioProject PRJNA688725
SRA SRP299826

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE164061_ES_LMNA_RNA_seq_differential_expression_Deseq2.xlsx 11.0 Mb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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