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Status |
Public on Jul 25, 2022 |
Title |
RBMS3_ACTD_3hr_REP1 |
Sample type |
SRA |
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Source name |
RBMS3_ACTD_3hr
|
Organism |
Homo sapiens |
Characteristics |
cell line background: HMLE cell type: Immortalized mammary epithelial cells genotype/variation: RbMS3 expression treament: treated with ACTD at 180 minutes
|
Treatment protocol |
the HMLE/LacZ and HMLE/RBMS3 cells were treated with 10 µg/mL of Actinomycin D for 4 different time points (0, 90, 180 and 360 mins).
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Growth protocol |
HMLE cells were cultured in 1:1 Dulbecco's Modified Eagle's Medium (DMEM)/HAMF12 medium (Invitrogen) complemented with 10% FBS (Cambrex), 100 U/ml penicillin-streptomycin (Invitrogen), 2 mM L glutamine (Invitrogen), 10 ng/ml human epidermal growth factor (EGF) (PromoCell), 0.5 µg/ml hydrocortisone (Sigma) and 10 µg/ml insulin (Sigma)
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Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with the RNeasy Plus mini kit (Qiagen) Library preparation using Lexogen's QuantSeq 3'mRNA-seq method. 75bp single reads with dual indexing.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Description |
RBMS3_ACTD_3hr_REP1_S46_L002
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Data processing |
FASTQ files trimmed using Trim Galore (v0.6.6) with default parameters, except: --three_prime_clip_R1 12 Trimmed FASTQ files were quantified using Salmon (v1.4.0) with default parameters, except: --validateMappings -l A Transcripts were mapped to genes using biomaRT (v2.48.1) and tximport (v1.20.0) Normalized gene counts were computed using DESeq2 (v1.32.0) counts(normalized=TRUE) Differential expression was computed using DESeq2 (v1.32.0) DESeq() Genome_build: Gencode v36 Supplementary_files_format_and_content: tab-delimited quant.sf text files generated by Salmon for each sample Supplementary_files_format_and_content: comma-delimited text file of normalized gene counts for all samples
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Submission date |
Jul 30, 2021 |
Last update date |
Jul 25, 2022 |
Contact name |
Guojun Wu |
Organization name |
Karmanos Cancer Institute
|
Department |
Oncology
|
Street address |
4100 John R
|
City |
Detroit |
State/province |
MI |
ZIP/Postal code |
48201 |
Country |
USA |
|
|
Platform ID |
GPL24676 |
Series (1) |
GSE181237 |
RNA binding protein RBMS3 is a common effector of EMT program that promotes Triple-Negative Breast Cancer Progression by Regulation of PRRX1 mRNA Stability |
|
Relations |
BioSample |
SAMN20507179 |
SRA |
SRX11613678 |