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Sample GSM7124048 Query DataSets for GSM7124048
Status Public on Feb 15, 2024
Title Mut 0hr replicate 1
Sample type SRA
 
Source name UOK262
Organism Homo sapiens
Characteristics cell line: UOK262
cell type: renal cell carcinoma
genotype: Mutant
treatment: 4-thiouridine
time: 0 hr
Treatment protocol Metabolic labeling to determine RNA half-life followed the method of Herzog et al. Cells were seeded the day before the experiment at approx. 50% confluency. The morning of the experiment, media was removed and replaced with cell media supplemented with 100 µM 4-thiouridine to begin the “pulse”. 4SU-containing media was exchanged every 8 hr during the 24 hr “pulse” period to increase the efficiency of labeling. Following 24 hr labeling, the “pulse” media was removed. Cells were washed 2X with PBS. Cell culture growth medium containing 10 mM uridine (i.e., 100X excess over 4SU) was added to the cells to begin the “chase”.
Extracted molecule total RNA
Extraction protocol At select time points of interest, “chase” media was removed, and cells were lysed in using Trizol Reagent according to the manufacture’s protocol with the following modifications: RNA isolation was performed in the dark and DTT was added to the aqueous phase to keep samples under reducing conditions.
Library preparation was performed using QuantSeq 3' mRNA library prep kit for Illumina using the manufacturer’s protocol and recommended maximum input amount
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 3000
 
Data processing Read quality analysis was performed with FastQC. Following the recommendation of Herzog et al., read 2 was discarded. Demultiplexed fastq files were applied to the SLAMDUNK pipeline (v/0.4.2) and mapped against hg38. The optional --multimappers flag was enabled. Following the pipeline, the output count file was collapsed used the included SLAMDUNK Alleyoop collapse module. Curve fitting was performed according to a first-order decay reaction in R (v3.6.3)
SLAMDUNK pipeline (v 0.4.2)
Assembly: hg38
Supplementary files format and content: tsv count file
 
Submission date Mar 30, 2023
Last update date Feb 15, 2024
Contact name Pedro J Batista
E-mail(s) pedro.batista@nih.gov
Phone 3014356294
Organization name National Institutes of Health
Department National Cancer Institute
Lab Cell Biology
Street address 37 Convent Street Bldg 37
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platform ID GPL21290
Series (2)
GSE228559 Rewiring of RNA methylation by the oncometabolite fumarate in renal cell carcinoma [SLAM-seq]
GSE228565 Rewiring of RNA methylation by the oncometabolite fumarate in renal cell carcinoma
Relations
BioSample SAMN33986893
SRA SRX19819990

Supplementary file Size Download File type/resource
GSM7124048_Mut_0hrA_S4_L008_R1_001.fastq_slamdunk_mapped_filtered_tcount_collapsed.csv.gz 472.9 Kb (ftp)(http) CSV
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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