NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2044420 Query DataSets for GSM2044420
Status Public on Dec 06, 2017
Title Healthy_DMSO_R2
Sample type SRA
 
Source name Healthy endothelial cells_DMSO
Organism Homo sapiens
Characteristics cell type: Human aortic endothelial cell
disease state: healthy
passages: 5-9
Treatment protocol Cells were stimulated with DMSO, SAHA (2 μM) or C646 (10 μM) for 12 hours. EP300 knock-down was generated using ON-TARGETplus Human EP300 (2033) siRNA – SMARTpool (L-003486-00-0005, Dharmacon). Cells were cultured in Opti-MEM® (Life Technologies) media with Lipofectamine® RNAiMAX Reagent (13778-075, Life Technologies) with either non-target (ON-TARGETplus Non-targeting Pool, D-001810-10-05, Dharmacon) or 25 nM EP300 siRNA for four hours. Media was replaced with EBM-2 and RNA was harvested after 48 hours.
Growth protocol Human aortic endothelial cells (HAEC) from diabetic (CC-2919) and non-diabetic (CC-2535) individuals were maintained in endothelial cell basal growth media-2 (EBM-2, Lonza) with additional EBM-2 growth factors and supplements and with 10% heat-inactivated fetal bovine serum (Gibco). HAECs used in this study were between 5-9 passages.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted in TRIzol (Invitrogen) and purified using the Direct-zolTM RNA MiniPrep kit (cat. no: R2052, Zymo Research) according to the manufacturers instructions. RNA was quantified on the MultiNA bioanalyzer (Shimadzu).
NEBNext® Poly(A) mRNA Magnetic Isolation Module was used to enrich mRNA from 1 μg of total RNA. The NEBNext® Ultra™ Directional RNA Library Prep Kit for Illumina® was used to generate barcodes. Libraries were quantified on the MultiNA bioanalyzer (Shimadzu) and pooled to equimolar ratios for sequencing. Cluster generation was performed at a concentration of 12 pM (TruSeq SR Cluster Kit v4-cBot-HS) and the flow cell was run on Illumina HiSeq2500 generating 50 nt reads.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Data processing Fastq files were aligned to the hg19 human genome (ensembl GRCh37 release 75) using STAR
The tool featureCounts was used to generate a matrix of read counts per gene
edgeR software was then used to determine differential gene expression
Genome_build: hg19
Supplementary_files_format_and_content: Matrix (text file) of raw reads for each gene (ensembl GRCh37 release 75) for all samples
 
Submission date Jan 21, 2016
Last update date May 15, 2019
Contact name Assam El-Osta
Organization name Baker Heart and Diabetes Institute
Lab Human Epigenetics
Street address 75 Commercial Road
City Melbourne
ZIP/Postal code 3004
Country Australia
 
Platform ID GPL16791
Series (1)
GSE77108 HDAC inhibitor SAHA reverses inflammatory gene expression in diabetic endothelial cells
Relations
BioSample SAMN04432988
SRA SRX1540340

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap