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SRX22858149: GSM7966620: HEK293T ΔYB-1ΔYB-3 + YB-3, Ribo-Seq, rep3; Homo sapiens; OTHER
2 ILLUMINA (Illumina HiSeq 2000) runs: 63.2M spots, 3.3G bases, 1.1Gb downloads

External Id: GSM7966620_r1
Submitted by: Institute of Protein Research
Study: Changes in transcriptome and translatome upon YB-1 or YB-3 expression in double knockout HEK293T ?YB-1?YB-3 cells
show Abstracthide Abstract
In this study, we generated transcriptome profiles from HEK293T, HEK293T ?YB-1?YB-3, and HEK293T ?YB-1?YB-3 with the restored expression of YB-1 and/or YB-3. The data are used to explore YB-1 and YB-3 influence on transcriptome and translatome and their functional interchangeability in transcription and translation. Overall design: We established double knockout HEK293T ?YB-1?YB-3 cells with the CRISPR/Cas approach. Next, we obtained derivatives of the double knockout HEK293T?YB-1?YB-3 cells stably expressing full-length YB-1 and/or YB-3 mRNA. RNA-Seq and Ribo-Seq data obtained from HEK293T, HEK293T ?YB-1?YB-3, and HEK293T ?YB-1?YB-3 with restored YB-1 and/or YB-3 expression in normal conditions.
Sample: HEK293T ΔYB-1ΔYB-3 + YB-3, Ribo-Seq, rep3
SAMN38765412 • SRS19833684 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: GSM7966620
Instrument: Illumina HiSeq 2000
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: SINGLE
Construction protocol: Cells were chilled on ice and washed with PBS + cycloheximide (100 µg/ml), lysed with buffer containing 20 mM Tris-HCl (pH 7.4), 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide (Sigma-Aldrich), 25 U/ml TURBO DNase (Ambion). The lysate was divided into two parts for Ribo-Seq and RNA-Seq library preparation. Nuclease footprinting and ribosome recovery for Ribo-Seq library preparation were performed according to (McGlincy 2017, PMID: 28579404). The adapter for Ribo-Seq had a UMI-sequence (5 random nucleotides) for deduplication. Total RNA for RNA-Seq library preparation was isolated using TRIzol LS Reagent (Thermo Fisher Scientific). The rRNA depletion was performed using a RiboMinus™ Eukaryote Kit v2 (Thermo Fisher Scientific) according to the manufacturer's recommendations. RNA-Seq libraries were constructed using a NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). Ribo-Seq libraries were obtained according to (McGlincy 2017, PMID: 28579404) using CircLigase II (Lucigen), custom adapter with UMI-sequence (5 random nucleotides), and NEBNext Multiplex Oligos for Illumina Index Primers Set (NEB).
Runs: 2 runs, 63.2M spots, 3.3G bases, 1.1Gb
Run# of Spots# of BasesSizePublished
SRR27177549364,21054.6M21.5Mb2024-01-19
SRR2717755062,804,5353.2G1.1Gb2024-01-19

ID:
30907591

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