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Sample GSM4211200 Query DataSets for GSM4211200
Status Public on Mar 20, 2020
Title ΔelyC rep1_37°C
Sample type SRA
 
Source name ΔelyC_37°C
Organism Escherichia coli
Characteristics genotype/variation: elyC::frt (EM9)
treatment: Grown at 37°C, harvested at OD600nm 0.3-0.35
Treatment protocol The pellets were washed once with cold TES buffer (100 mM NaCl, 1 mM EDTA, 10 mM Tris hydrochloride [pH 7.4]), recentrifuged, and cells snap-frozen in liquid nitrogen and stored at −85 °C.
Growth protocol The pre-cultures were grown in LB medium at 37°C. Triplicate cultures of the wild-type and ∆elyC mutant strains were grown in 250 ml LB 1% NaCl liquid media, 250 rpm, at 21°C and 37°C to early-log phase (OD600 of 0.30 to 0.35). The samples were immediately centrifuged (6000 g) at 4 °C for 5 min.
Extracted molecule total RNA
Extraction protocol Total RNA was purified using the RNeasy Mini Kit (QIAGEN) with the RNAprotect Bacteria reagent (QIAGEN) according to the manufacturer’s protocol. DNA was removed using RNase-Free DNase set from QIAGEN. The RNA was finally resuspended in RNase-Free Water (QIAGEN) and RNA concentration was quantified using the NanoDrop ND-1000 at 260 nm. RNA Ribosome Integrity Numbers (RIN) and purity of the RNA samples were assessed using the Agilent Bioanalyzer 2100 and RNA 6000 Pico Kit. The RIN numbers for all the twelve samples were 9.3 to 10. The rRNA depletion was performed using the Ribo-Zero Magnetic Gold Kit for Gram-negative Bacteria (Illumina).
RNAseq libraries were prepared using KAPA RNA stranded Kit (Roche-Nimblegen). Libraries were assessed and quantified by BioAnalyzer using the High Sensitivity DNA Kit (Agilent). Sequencing was performed on an Illumina HiSeq2000 machine, in 75-nucleotide paired-end mode.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description 37c_em9_1
HI.2835.005.Index_16.IK_37C-EM9-1
Data processing Poor quality reads were trimmed out with Trimmomatic software. The quality of the reads, before and after trimming, was assessed with FASTQC version 0. 11. 5.
The reads were aligned to the E. coli sub-strain MG1655 reference genome (GCA000801205.1) with Bowtie2 version 2. 2. 9. The reference genome used for the alignment, and the GTF annotation file used for counting the number of reads aligned to each feature, were downloaded from Ensembl (release 27). The aligned data saved as BAM files. The raw alignment read counts for each gene were calculated using featureCounts 1.5.1.
Normalization and differential expression (fold change /Log2 fold change) of genes from the raw alignment counts were determined with a significant p-values (< 0.05) using the DESeq 2. 1. 14.0 in the R program.
Genome_build: GCA000801205.1
Supplementary_files_format_and_content: The output from DESeq2, including the raw counts, normalized relative to the total number of reads. Differentially expressed genes were determined with a p-value (< 0.05), and as part of the multiple comparison testing, significant Benjamini-Hochberg adjusted p-values (p-adj) < 0.05 (5% false discovery rate) were considered. In addition to the counts normalized relative to the library size, the genome-wide occupancy (quantitation) was also computed into density units of fragments per kilobase of exon model per million reads mapped (FPKM).
 
Submission date Dec 09, 2019
Last update date Mar 20, 2020
Contact name Fardin Ghobakhlou
Organization name University of Montreal
Department Microbiology , Infectiology and Immunology
Lab Dr. Paradis-Bleau
Street address Pavillon Roger-Gaudry, S-640 2900 Boulevard Edouard-Montpetit, Montréal, QC
City Montreal
State/province QC
ZIP/Postal code H3T 1J4
Country Canada
 
Platform ID GPL14548
Series (1)
GSE141694 Phenotypic and transcriptomic characterization of ElyC-defective Escherichia coli cells reveal the importance of ElyC in cell envelope biosynthesis at optimal and sub-optimal temperatures
Relations
BioSample SAMN13514091
SRA SRX7291204

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

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