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Series GSE77325 Query DataSets for GSE77325
Status Public on Feb 06, 2016
Title Gene expression analysis of E. coli strains provides insights into the role of gene regulation in diversification
Organism Escherichia coli
Experiment type Expression profiling by high throughput sequencing
Summary Escherichia coli spans a genetic continuum from enteric strains to several phylogenetically distinct, atypical lineages that are rare in humans, but more common in extra-intestinal environments. To investigate the link between gene regulation, phylogeny and diversification in this species, we analyzed global gene expression profiles of four strains representing distinct evolutionary lineages, including a well-studied laboratory strain, a typical commensal (enteric) strain and two environmental strains. RNA-Seq was employed to compare the whole transcriptomes of strains grown under batch, chemostat and starvation conditions. Highly differentially expressed genes showed a significantly lower nucleotide sequence identity compared with other genes, indicating that gene regulation and coding sequence conservation are directly connected. Overall, distances between the strains based on gene expression profiles were largely dependent on the culture condition and did not reflect phylogenetic relatedness. Expression differences of commonly shared genes (all four strains) and E. coli core genes were consistently smaller between strains characterized by more similar primary habitats. For instance, environmental strains exhibited increased expression of stress defense genes under carbon-limited growth and entered a more pronounced survival-like phenotype during starvation compared with other strains, which stayed more alert for substrate scavenging and catabolism during no-growth conditions. Since those environmental strains show similar genetic distance to each other and to the other two strains, these findings cannot be simply attributed to genetic relatedness but suggest physiological adaptations. Our study provides new insights into ecologically relevant gene-expression and underscores the role of (differential) gene regulation for the diversification of the model bacterial species.
 
Overall design Four E.coli strains, laboratory strain K12 (MG1655), a commensal model strain (IAI1), a soil-isolated strain (TW11588-Clade IV), and a freshwater-isolated strain (TW09308—Clade V) were used. Each strain was grown on a minimal growth medium (Ihssen and Egli, 2004) in three treatment modes: chemostat, batch, and starvation. Cells from batch culture were collected when reaching steady-state. For starvation, the medium flow was stopped during steady-state and bacteria were collected after 4 h.
 
Contributor(s) Vital M, Chai B, Østman B, Cole JR, Konstantinidis KT, Tiedje JM
Citation(s) 25343512
Submission date Jan 28, 2016
Last update date May 15, 2019
Contact name Benli Chai
E-mail(s) chaibenl@msu.edu
Phone 517-353-3842
Organization name Michigan State University
Department Center for Microbial Ecology
Street address 567 Wilson Road Rm 2225 A
City East Lansing
State/province Michigan
ZIP/Postal code 48824
Country USA
 
Platforms (1)
GPL14548 Illumina HiSeq 2000 (Escherichia coli)
Samples (24)
GSM2049254 MG1655 transcriptome from chemostat growth_1
GSM2049255 MG1655 transcriptome from batch growth_1
GSM2049256 MG1655 transcriptome from starvation growth_1
Relations
BioProject PRJNA310115
SRA SRP069023

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Supplementary file Size Download File type/resource
GSE77325_Gene_annotations.txt.gz 157.4 Kb (ftp)(http) TXT
GSE77325_normalized_count.txt.gz 756.6 Kb (ftp)(http) TXT
GSE77325_panGeneMap.txt.gz 197.8 Kb (ftp)(http) TXT
GSE77325_raw_count.txt.gz 186.2 Kb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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