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Series GSE45689 Query DataSets for GSE45689
Status Public on Feb 20, 2014
Title Comparison of the expression profiles of the Clostridium difficile 630E strain and a spoIIID mutant after 15h of growth
Organism Clostridioides difficile
Experiment type Expression profiling by array
Summary Compartment-specific control of gene expression during Bacillus subtilis sporulation is governed by a cascade of four sigma factors, sigmaF and sigmaG in the forespore and sigmaE and sigmaK in the mother cell. In this work, we combined transcriptional analyses and transcriptional start site mapping to define the sigmaF, sigmaE, sigmaG and sigmaK regulons in Clostridium difficile. A total of about 225 genes were under the control of these sigma factors: 25 in the sigmaF regulon, 97 sigmaE-dependent genes, 50 sigmaG-governed genes and 56 genes specifically controlled by sigmaK. A significant fraction of genes in each regulon are of unknown function and we can propose new candidates for spore coat proteins synthesized under the control of sigmaE and sigmaK among proteins previously detected in the spore proteome (Lawley et al., 2009 (PMID 19542279)). Global analysis of developmental gene expression under the control of these sigma factors indicate deviations from the B. subtilis model regarding the communication between mother cell and forespore in C. difficile. We show that the expression of the sigmaE regulon in the mother cell is not strictly under the control of sigmaF despite the fact that the forespore product SpoIIR is required for the processing of pro-sigmaE. In addition, the sigmaK regulon is not controlled by sigmaG in C. difficile in connection with the lack of pro-sigmaK processing in this bacterium. However, a control of the forespore on sigmaK targets is maintained through a sigmaF-dependent regulation of sigmaK-controlled genes, a process that bypasses sigmaG. We also performed a transcriptome experiment of the spoIIID mutant compared to the 630E strain and showed that SpoIIID represses the expression of SigE target genes and activates the expression of sigK.
 
Overall design Transcriptional profiling of the C. difficile 630E strain vs. a spoIIID mutant after 15h of growth in MS. Two-condition experiment: 630E strain 15h vs. spoIIID mutant 15h. 2 biological replicates for each condition.
 
Contributor(s) Saujet L, Monot M
Citation(s) 24098137
Submission date Apr 01, 2013
Last update date Feb 21, 2014
Contact name Monot Marc
E-mail(s) [email protected]
Phone +33145688390
Organization name Institut Pasteur
Department Genomes and Genetics
Lab Biomics
Street address 25, rue du docteur roux
City Paris
ZIP/Postal code 75015
Country France
 
Platforms (1)
GPL10556 Agilent-020954 Clostridium difficile Expression 15.7k array
Samples (2)
GSM1111964 CD630_WT1-cy3_SpoIIID1-cy5
GSM1111965 CD630_WT2-cy5_spoIIID2-cy3
This SubSeries is part of SuperSeries:
GSE43202 Comparison of the expression profiles of the 630E JIR8094 strain and sporulation sigma factor mutants (sigE, sigF, sigG, sigK, spoIIID) in MS
Relations
BioProject PRJNA195612

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE45689_RAW.tar 2.4 Mb (http)(custom) TAR (of GPR)
GSE45689_readme.txt 552 b (ftp)(http) TXT
GSE45689_spoIIID-WT_Result_files.xls.gz 398.1 Kb (ftp)(http) XLS
Processed data included within Sample table
Processed data are available on Series record

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