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SRX7651648: GSM4290267: RpoABC_ChIP-Seq_∆citA(MB2529)_(AIYT-162); Caulobacter vibrioides NA1000; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 19.1M spots, 955.5M bases, 313.9Mb downloads

Submitted by: NCBI (GEO)
Study: Polymerase occupancy (ChIP-Seq) in WT and mutants of Caulobacter crescentus NA1000
show Abstracthide Abstract
Coordination of cell cycle progression with central metabolism is fundamental to all cell types and likely underlies differentiation into dispersal cells in bacteria. How central metabolism is monitored to regulate cell cycle functions is poorly understood. A forward genetic selection for cell cycle regulators in the polarized alpha-proteobacterium Caulobacter crescentus unearthed the uncharacterized CitA citrate synthase, a TCA (tricarboxylic acid) cycle enzyme, as unprecedented checkpoint regulator of the G1?S transition. We show that loss of the CitA protein provokes a (p)ppGpp alarmone-dependent G1-phase arrest without apparent metabolic or energy insufficiency. While S-phase entry is still conferred when CitA is rendered catalytically inactive, the paralogous CitB citrate synthase has no overt role other than sustaining TCA cycle activity when CitA is absent. With eukaryotic citrate synthase paralogs known to fulfill regulatory functions, our work extends the moonlighting paradigm to citrate synthase coordinating central (TCA) metabolism with development and perhaps antibiotic tolerance in bacteria. Overall design: Examination of polymerase whole genome binding/occupancy (ChIP-Seq) in WT Caulobacter crescentus and comparison with ?citA mutant or a strain producing the (p)ppGpp alarmone. 3 samples were analyzed in monoplicate
Sample: RpoABC_ChIP-Seq_∆citA(MB2529)_(AIYT-162)
SAMN13945460 • SRS6081104 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 4000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: SINGLE
Construction protocol: After resuspension of the cells in TES buffer (10 mM Tris-HCl pH 7.5, 1 mM EDTA, 100 mM NaCl) containing 10 mM of DTT, they were incubated in the presence of Ready-Lyse lysozyme solution (Epicentre, Madison, WI) for 10 minutes at 37°C, according to the manufacturer's instructions. Lysates were sonicated (Bioruptor® Pico) at 4°C using 15 bursts of 30 sec to shear DNA fragments to an average length of 0.3-0.5 kbp and cleared by centrifugation at 14,000 rpm for 2 min at 4°C. The volume of the lysates was then adjusted (relative to the protein concentration) to 1 ml using ChIP buffer (0.01% SDS, 1.1% Triton X-84 100, 1.2 mM EDTA, 16.7 mM Tris-HCl [pH 8.1], 167 mM NaCl) containing protease inhibitors (Roche) and pre-cleared with 80 μl of protein-G agarose (Roche, www.roche.com) and 100 μg BSA. The rest of the pre-cleared lysates was incubated overnight at 4°C with E. coli RNA polymerase antibody sampler kit (Cat 699907, Biolegend https://www.biolegend.com/fr-ch/products/e--coli-rna-polymerase-antibody-sampler-kit-15078) with the different antibodies mixed with a ratio of 1:1:1 (1:500 dilution). The immuno-complexes were captured after incubation with Protein-G agarose (pre-saturated with BSA) during a 2 h incubation at 4°C and they were washed subsequently with low salt washing buffer (0.1% SDS, 1% Triton X-100, 2 mM EDTA, 20 mM Tris-HCl pH 8.1, 150 mM NaCl), with high salt washing buffer (0.1% SDS, 1% Triton X-100, 2 mM EDTA, 20 mM Tris-HCl pH 8.1, 500 mM NaCl), with LiCl washing buffer (0.25 M LiCl, 1% NP-40, 1% deoxycholate, 1 mM EDTA, 10 mM Tris-HCl pH 8.1) and finally twice with TE buffer (10 mM Tris-HCl pH 8.1, 1 mM EDTA). The complexes were eluted from the Protein-G agarose beads with two times 250 μl elution buffer (SDS 1%, 0.1 M NaHCO3, freshly prepared) and then, incubated overnight with 300 mM NaCl at 65°C to reverse the crosslinks. The samples were then treated with 2 μg of Proteinase K for 2 h at 45°C in 40 mM EDTA and 40 mM Tris-HCl (pH 6.5). DNA was extracted using phenol:chloroform:isoamyl alcohol (25:24:1), ethanol-precipitated using 20 μg of glycogen as a carrier and resuspended in 50 μl of DNAse/RNAse free water. Immunoprecipitated chromatin was used to prepare sample libraries used for deep-sequencing at Fasteris SA (Geneva, Switzerland). ChIP-Seq libraries were prepared using the DNA Sample Prep Kit (Illumina) following manufacturer instructions. TruSeq ChIP Library Preparation Kit
Experiment attributes:
GEO Accession: GSM4290267
Links:
Runs: 1 run, 19.1M spots, 955.5M bases, 313.9Mb
Run# of Spots# of BasesSizePublished
SRR1099023719,110,680955.5M313.9Mb2020-03-19

ID:
9982510

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