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Series GSE245270 Query DataSets for GSE245270
Status Public on Oct 17, 2023
Title β2-adrenergic receptor transcriptional response in HEK293 wild type, β-arrestin1/2 KO and Gαs KO cells upon isoproterenol stimulation.
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary The role of nuclear signaling by β2-adrenergic receptor (β2AR) through β-arrestins in the absence of a functional Gαs protein has not been evaluated. This has prevented a comprehensive understanding of the relative contribution of Gαs and β-arrestins to the overall β2AR signaling, thereby limiting our appreciation of how β-arrestin- or Gαs-biased ligands may affect their therapeutic outcomes. To explore the role of Gαs and β-arrestin in nuclear transcriptional programs in a global unbiased approach, we performed RNA sequencing studies in cells lacking either of these two signaling arms downstream from β2AR, followed by detailed bioinformatics analysis of gene expression signatures. We noticed multiple genes whose individual expression levels were distinct in β-arrestin1/2 and Gαs KO cells. Rather than focusing on the individual gene level, we performed a detailed analysis of gene signatures taking advantage of large datasets that were recently compiled as part of the Molecular Signatures Database (MSigDB). This approach supported that β-arrestins are not required for the activation of PKA gene signatures, including prior datasets of forskolin and CREB1 targets, while Gαs is essential. β2AR activation also led to significant changes in multiple MAPK signatures, which clearly support the activation of MAPK nuclear transcriptional programs by these receptors. Although individual variations do exist reflecting the complexities of β-arrestin- and Gαs-mediated signaling events, stimulation of these MAPK regulated gene signatures was not significantly reduced in β-arrestin1/2 KO cells but abolished in Gαs KO cells.
 
Overall design HEK293 wild type, β-arrestin1/2 KO and Gαs KO cells transiently overexpressing wild type β2-adrenergic receptor were stimulated with isoproterenol or vehicle for 1 h in triplicates. We performed differential gene expression analysis using data obtained from RNAseq. We also obtained enrichment profiles for gene sets related to PKA and MAPK pathways.
 
Contributor(s) Burghi V, Officer A, Wu X, Gutkind JS
Citation(s) 37774973
Submission date Oct 12, 2023
Last update date Jul 05, 2024
Contact name Valeria Burghi
E-mail(s) valeburghi@gmail.com
Organization name University of California San Diego
Department Pharmacology
Street address 3855 Health Sciences Drive, Room 2345
City La Jolla
ZIP/Postal code 92093
Country USA
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (18)
GSM7840043 HEK293 cells, wild type, basal, biol rep 1
GSM7840044 HEK293 cells, wild type, basal, biol rep 2
GSM7840045 HEK293 cells, wild type, basal, biol rep 3
Relations
BioProject PRJNA1027499

Download family Format
SOFT formatted family file(s) SOFTHelp
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Supplementary file Size Download File type/resource
GSE245270_all_salmon_counts_-_all_samples.csv.gz 5.3 Mb (ftp)(http) CSV
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Raw data are available in SRA

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