NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE79880 Query DataSets for GSE79880
Status Public on Nov 28, 2016
Title Conserved local hypomethylation control during the bacterial cell cycle and by superimposed environmental cues
Organisms Sinorhizobium meliloti; Vibrio cholerae O1 biovar El Tor; Caulobacter vibrioides; Escherichia coli str. K-12 substr. MG1655; Caulobacter vibrioides NA1000
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Methylation profiling by high throughput sequencing
Summary Heritable DNA methylation imprints occur in most genomes and underlie genetic variability in humans. The mechanism and consequences of establishing and propagating local hypomethylation through consecutive rounds of DNA replication and intermittent cell division cycles are poorly understood. Our genome-wide and site-specific methyl-N6-adenine (m6A-) analyses reveal a conserved local hypomethylation mechanism in two α-proteobacterial model systems. We show that MucR, a DNA-binding protein that uses an ancestral zinc-finger fold to control expression of virulence and cell cycle genes, competes with the cell cycle-regulated adenine-methyltransferase CcrM for target sites in S-phase, but not in G1-phase. Constitutive expression of CcrM or heterologous methylases during the cell cycle homogenizes m6A patterns even when MucR is present and controls transcription. We also find that environmental responses can impose methylation remodelling at certain sites, while the conserved cell cycle circuitry imposes systemic constraints on when local hypomethylation is instated.
 
Overall design 4 ChIPseq samples in synchronized C. crescentus cells, SMRT methylation profiles of Wild type and ∆mucR1 ∆mucR2 cells, 6 RECseq samples in Wildtype C. crescentus, E. coli, S. meliloti, V. cholera El Tor and in mucR1 mutants of C. crescentus and S. meliloti.
 
Contributor(s) Ardissone S, Redder P, Russo G, Frandi A, Fumeaux C, Patrignani A, Schlapbach R, Viollier PH
Citation(s) 27997543
Submission date Apr 04, 2016
Last update date May 15, 2019
Contact name Antonio Frandi
E-mail(s) [email protected]
Organization name University of Geneva
Department Microbiology and Molecular Medicine
Lab Patrick Viollier Lab
Street address rue michel servet 1
City Geneva
ZIP/Postal code 1211
Country Switzerland
 
Platforms (7)
GPL18006 Illumina HiSeq 2500 (Caulobacter vibrioides)
GPL18956 Illumina HiSeq 2500 (Escherichia coli str. K-12 substr. MG1655)
GPL21317 Illumina HiSeq 2500 (Caulobacter crescentus NA1000)
Samples (16)
GSM2107771 MucR1_ChIP_exo_T10
GSM2107772 MucR1_ChIP_exo_T40
GSM2107773 MucR1_ChIP_exo_T70
Relations
BioProject PRJNA317321
SRA SRP072878

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
GSE79880_RAW.tar 197.5 Mb (http)(custom) TAR (of CSV, GFF, 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