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SRX2969622: GSM2690557: WT_g40; Caulobacter vibrioides NA1000; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 6.8M spots, 546.2M bases, 265.3Mb downloads

Submitted by: NCBI (GEO)
Study: A bacterial chromosome structuring protein binds overtwisted DNA to stimulate type II topoisomerases and enable DNA replication
show Abstracthide Abstract
When DNA is unwound during replication, it becomes overtwisted and forms positive supercoils in front of the translocating DNA polymerase. Unless removed or dissipated, this superhelical tension can impede replication elongation. Topoisomerases, including gyrase and topoisomerase IV in bacteria, are required to relax positive supercoils ahead of DNA polymerase, but may not be sufficient for replication. Here, we find that GapR, a chromosome structuring protein in Caulobacter crescentus, is required to complete DNA replication. GapR associates in vivo with positively supercoiled chromosomal DNA, and our biochemical and structural studies demonstrate that GapR forms a dimer-of-dimers that fully encircles overtwisted DNA. Further, we show that GapR stimulates gyrase and topo IV to relax positive supercoils, thereby enabling DNA replication. Analogous chromosome structuring proteins that locate to the overtwisted DNA in front of replication forks may be present in other organisms, similarly helping to recruit and stimulate topoisomerases during DNA replication. Overall design: Sequencing experiments from Caulobacter crescentus CB15N wild-type, GapR-3xFLAG, and GapR-depleted cells. (i) RNA-seq after GapR depletion, (ii) GapR-3xFLAG ChIP-seq, (iii) cell-cycle DNA-seq after GapR depletion.
Sample: WT_g40
SAMN07299091 • SRS2326180 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: PAIRED
Construction protocol: Libraries were constructed by end repairing DNA with T4 DNA polymerase (NEB), T4 PNK (NEB), and Klenow large fragment (NEB). 3' overhangs were added with Klenow (3'→5' exo-) (NEB). Y-shaped Illumina adapters were ligated onto the DNA, and libraries were amplified with either Phusion (NEB) or Kapa HiFi Polymerase (Kapa Biosystems). Libraries were size selected to be 250-600 bp.
Experiment attributes:
GEO Accession: GSM2690557
Links:
Runs: 1 run, 6.8M spots, 546.2M bases, 265.3Mb
Run# of Spots# of BasesSizePublished
SRR57721856,827,576546.2M265.3Mb2018-09-13

ID:
4232389

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