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SRX11502884: GSM5462577: WT_TREAT_3; Salmonella enterica subsp. enterica serovar Typhimurium; RNA-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 7M spots, 1.4G bases, 870.9Mb downloads

Submitted by: NCBI (GEO)
Study: Transcriptional Sequencing of Salmonella enterica serovar Typhimurium wild typle and DsrA-deletion mutant Survival unfer LB or H2O2 conditions
show Abstracthide Abstract
To elucidated the regulatory effect of DsrA on the oxidative resistance in Salmonella enterica serovar Typhimurium. RNA sample of wild-type and DsrA-deletion strain that grown in LB medium or H2O2 stress were extracted. Three biological replicates were carried out per sample. RNA sample was sequenced with Illumina HiSeq 4000 System. DESeq2 method was used to calculate the differentially expressed genes. qRT–PCR and gene mutation were used to validate RNA-seq result. Overall design: wild-type in LB (WT_CK), wild-type in H2O2(WT_TREAT), dsrA mutant in LB(MT_CK), dsrA in H2O2 (MT_TREAT) Three biological repetitions of each samle, totally 12 samples were conducted RNA sequncing.
Library:
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA was extracted using TRIzol Reagent (Invitrogen, CAS 15596026) according to the manual.RNA quality and integrity was verified by electrophoretic analysis and UV spectroscopy using NanoDrop and Agilent 2100 instruments. The RNA integrity number for all samples were between 8.2 and 9.7. The Strand-specific transcriptome library construction and RNA sequencing was done as follow. Briefly, 1 µg total RNA was digested with DNase I (Thermo Scientific) and treated with Ribo-Zero Magnetic Gold Kit (Epicenter) to deplete rRNA. The protocol of TruSeq RNA Sample Prep Kit v2 (Illumina) was used to construct the libraries. The RNA was fragmented into small pieces and first-strand cDNA was generated using Super Script II (Invitrogen). The products were purified and used in a Second Strand Master Mix containing dATP, dGTP, dCTP and dUTP. The purified fragmented cDNA was end-repaired and purified and A-tailed and adapters were attached. The purified product was digested with uracil-N-glycosylase to remove the dUTP containing second strand cDNA, followed by several rounds of PCR amplification to enrich the cDNA fragments. The PCR products were purified and the libraries were assessed using the Agilent 2100 Bioanalyzer and qPCR.
Experiment attributes:
GEO Accession: GSM5462577
Links:
Runs: 1 run, 7M spots, 1.4G bases, 870.9Mb
Run# of Spots# of BasesSizePublished
SRR151963226,996,0441.4G870.9Mb2022-02-15

ID:
15414751

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