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SRX8114665: GSM4476155: ChIP-Seq_TrcR_WTRm1021_S.meliloti_PYERif100; Sinorhizobium meliloti 2011; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 7.2M spots, 359.7M bases, 163.5Mb downloads

Submitted by: NCBI (GEO)
Study: The DUF1013 protein TrcR tracks with RNA polymerase to control bacterial cell cycle and protection against antibiotics (ChIP-seq dataset)
show Abstracthide Abstract
The regulatory roles of proteins associating with DNA-dependent RNA polymerase (RNAP) during transcription elongation are poorly characterized in bacteria. A forward genetic selection for Caulobacter crescentus cell cycle mutants revealed the uncharacterized DUF1013 protein (TrcR, transcriptional cell cycle regulator). TrcR associates with promoters and coding sequences (CDSs) and tracks with active RNAP. Loss of TrcR causes a cell division cycle and growth defect and an insufficiency in the essential cell cycle regulator CtrA. TrcR also protects cells from the quinolone antibiotic nalidixic acid that induces a multi-drug efflux pump and from the RNAP inhibitor rifampicin (Rif) that prevents transcription elongation. TrcR interacts biochemically and genetically with RNAP and no longer associates with chromatin when RNAP is inhibited with Rif. We show that these TrcR functions and its RNAP-dependent chromatin recruitment are conserved in symbiotic Sinorhizobium sp. and pathogenic Brucella sp., indicating that TrcR represents a new antibiotic target. Overall design: Examination of TrcR, RpoD and RNAP holoenzyme whole genome binding/occupancy (ChIP-Seq) in WT Caulobacter crescentus and mutants in PYE and following Rifampicin and Nalidixic Acid treatments and TrcR whole genome occupancy/binding in WT Sinorhizobium meliloti before and after Rifampicin treatment.
Sample: ChIP-Seq_TrcR_WTRm1021_S.meliloti_PYERif100
SAMN14596592 • SRS6479739 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 4000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: SINGLE
Construction protocol: Cells were lysed in a Ready-Lyse lysozyme solution (Epicentre Technologies) according to manufacturer's instructions and lysates were sonicated (Bioruptor® Pico) in an ice-water bath for 15 cycles 30 seconds ON and 30 seconds OFF, to shear DNA fragments to an average length of 0.3-0.5 kbp and cleared by centrifugation at 14,000 g for 2 minutes 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-100, 1.2 mM EDTA, 16.7 mM Tris-HCl (pH 8.1), 167 mM NaCl plus protease inhibitors (Roche, Switzerland) and pre-cleared with 80 μL of protein-A (rabbit antibodies) or –G (mouse antibodies) agarose (Roche) and 100 μg BSA. Ten percent of the supernatant was removed and used as total chromatin input DNA as described before (Delaby et al., 2019).Two microliters of polyclonal antibodies to TrcR, or of a mix of RNA polymerase from a monoclonal antibody sampler kit (ratio 1:1:1:1, Biolegend), or of monoclonal antibodies to σ70 (BioLegend, Mouse IgG2b) were added to the remains of the supernatant, incubated overnight at 4 °C with 80 μL of protein-A or -G agarose beads pre-saturated with BSA, washed once with low salt buffer (0.1% SDS, 1% Triton X-100, 2 mM EDTA, 20 mM Tris-HCl (pH 8.1) and 150 mM NaCl), high salt buffer (0.1% SDS, 1% Triton X-100, 2 mM EDTA, 20 mM Tris-HCl (pH 8.1) and 500 mM NaCl) and LiCl buffer (0.25 M LiCl, 1% NP-40, 1% sodium deoxycholate, 1 mM EDTA and 10 mM Tris-HCl (pH 8.1)), and twice with TE buffer (10 mM Tris-HCl (pH 8.1) and 1 mM EDTA). The protein DNA complexes were eluted in 500 μL freshly prepared elution buffer (1% SDS and 0.1 M NaHCO3), supplemented with NaCl to a final concentration of 300 mM and incubated overnight at 65 °C to reverse the crosslinks. The samples were 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 carrier and resuspended in 100 μL of 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's instructions.
Experiment attributes:
GEO Accession: GSM4476155
Links:
Runs: 1 run, 7.2M spots, 359.7M bases, 163.5Mb
Run# of Spots# of BasesSizePublished
SRR115445677,194,663359.7M163.5Mb2021-02-03

ID:
10564546

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