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Series GSE81584 Query DataSets for GSE81584
Status Public on May 01, 2017
Title Mfd alters global transcription patterns in undamaged Escherichia coli cells
Organism Escherichia coli
Experiment type Expression profiling by high throughput sequencing
Summary We uncovered evidence for an expanded role of transcription-coupled repair factor Mfd in Escherichia coli. In mfd knockout cells, expression of 75 genes was significantly increased while that of 18 genes was diminished. GO term analysis revealed that the affected genes were disproportionately from certain functional groups. RNA levels in the knockout deviated from wild type beginning at transcription start sites, arguing against premature termination as the cause. RNA-seq analysis in cells overexpressing Mfd revealed dramatic deviation of gene expression in the chromosome terminus region. Taken together, our data support a novel role for Mfd in transcription regulation.
 
Overall design Examination of E coli mfd knockdown and Mfd-overexpressing cells compared to wildtype E. coli controls
 
Contributor(s) Krasich R, Kreuzer KN
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date May 18, 2016
Last update date May 15, 2019
Contact name Rachel Krasich
Organization name NIEHS
Street address 111 TW Alexander Dr
City Research Triangle Park
State/province NC
ZIP/Postal code 27709
Country USA
 
Platforms (1)
GPL14548 Illumina HiSeq 2000 (Escherichia coli)
Samples (10)
GSM2157648 MG1655_1
GSM2157649 MG1655_2
GSM2157650 MG1655_3
Relations
BioProject PRJNA322690
SRA SRP075662

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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE81584_ANOVA_analysis_of_mfd-_cell_lines.xlsx 651.7 Kb (ftp)(http) XLSX
GSE81584_Mfd_overexpress_RPKM_values.txt.gz 185.8 Kb (ftp)(http) TXT
GSE81584_mfd-_bin100_counts.xlsx 5.1 Mb (ftp)(http) XLSX
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Raw data are available in SRA
Processed data are available on Series record

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