NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE72472 Query DataSets for GSE72472
Status Public on Mar 23, 2016
Title Characterization of the TcpP Regulon Vibrio cholerae El Tor
Organism Vibrio cholerae O1 str. C6706
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary The transcriptional factor ToxR initiates a virulence regulatory cascade required for V. cholerae to express critical host colonization factors and cause disease. Genome-wide expression studies suggest that ToxR regulates many genes important for V. cholerae pathogenesis, yet our knowledge of the direct regulon controlled by ToxR is limited to just four genes. Here, we determine ToxR’s genome-wide DNA-binding profile and show that ToxR is a global regulator of both progenitor genome-encoded genes and horizontally acquired islands encoding the majority of V. cholerae’s major virulence factors. Our results suggest that ToxR has gained regulatory control over important acquired elements that not only drive V. cholerae pathogenesis but that also define the major transitions of V. cholerae pandemic lineages. We demonstrate that ToxR shares nearly half its regulon with the histone-like nucleoid structuring protein H-NS, and antagonizes H-NS for control of critical colonization functions. This regulatory interaction is the major role of ToxR in V. cholerae colonization since deletion of H-NS abrogates the need of ToxR in V. cholerae host colonization. By comparing the genome-wide binding profiles of ToxR and other critical virulence regulators, we show that despite similar predicted DNA binding requirements, ToxR is unique in its global control of progenitor-encoded and acquired genes. Our results suggest that, like H-NS, factors in addition to linear DNA sequence drive selection of ToxR binding sites.
 
Overall design We used ChIP-seq to identify TcpP binding sites across the genome to determine the direct regulon of TcpP
 
Contributor(s) Kazi MI, Davies BW
Citation(s) 27070545
Submission date Aug 27, 2015
Last update date May 15, 2019
Contact name Bryan Davies
E-mail(s) [email protected]
Organization name University of Texas at Austin
Street address 2506 Speedway
City Austin
State/province TX
ZIP/Postal code 78712
Country USA
 
Platforms (1)
GPL15333 Illumina HiSeq 2000 (Vibrio cholerae O1 str. C6706)
Samples (3)
GSM1863018 TcpP ChIP control
GSM2079442 TcpP ChIP A
GSM2079443 TcpP ChIP B
This SubSeries is part of SuperSeries:
GSE72474 ToxR Antagonizes H-NS Regulation of Horizontally Acquired Genes to Drive Host Colonization.
Relations
BioProject PRJNA294112
SRA SRP062921

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
GSE72472_RAW.tar 10.0 Kb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap