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SRX16020051: GSM6288269: L1666-Haloferax_volcanii_stationary_ATAC_1pFA_rep1; Haloferax volcanii DS2; ATAC-seq
1 ILLUMINA (NextSeq 550) run: 1.8M spots, 140.4M bases, 53.6Mb downloads

External Id: GSM6288269_r1
Submitted by: Genetics, Stanford University
Study: The chromatin landscape of the euryarchaeon Haloferax volcanii
show Abstracthide Abstract
Archaea, together with Bacteria, represent the two main divisions of life on Earth, with many of the defining characteristics of the more complex eukaryotes tracing their origin to evolutionary innovations first made in their archaeal ancestors. One of the most notable such features is nucleosomal chromatin, although archaeal histones and chromatin differ significantly from those of eukaryotes. Despite increased interest in archaeal histones in recent years, the properties of archaeal chromatin have been little studied using genomic tools. Here, we adapt the ATAC-seq assay to the archaeal context and use it to map the accessible landscape of the genome of the euryarchaeote Haloferax volcanii. We integrate the resulting datasets with genome-wide maps of active transcription and single-stranded DNA (ssDNA), and find that while H. volcanii promoters exist in a preferentially accessible state, modulation of transcriptional activity is not associated with changes in promoter accessibility, unlike the typical situation in eukaryotes. Applying orthogonal single-molecule footprinting methods, we quantify the absolute levels of physical protection of H. volcanii, and find that archaeal nucleosomal chromatin is at its baseline comparably to slightly more open than that of eukaryotes. We also evaluate the degree of coordination of transcription within archaeal operons and make the unexpected observation that some CRISPR arrays are associated with highly prevalent ssDNA structures. These results provide a foundation for the future functional studies of archaeal chromatin. Overall design: KAS, ATAC-seq, NOME-seq, dSMF
Sample: L1666-Haloferax_volcanii_stationary_ATAC_1pFA_rep1
SAMN29500493 • SRS13700295 • All experiments • All runs
Library:
Name: GSM6288269
Instrument: NextSeq 550
Strategy: ATAC-seq
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: Cells were fixed by adding 37% formaldehyde (Sigma) at a final concentration of 1% and incubating for 15 minutes at room temperature. Formaldehyde was then quenched using 2.5 M Glycine at a final concentration of 0.25 M. Cells were subsequently centrifuged at 10,000 g for 2 minutes, washed once in 1x PBS, and centrifuged again at 10,000 g for 2 minutes. Transposition was carried out as above for 15 minutes. The reaction was stopped with the addition of 150 uL IP Elution Buffer (1% SDS, 0.1M NaHCO3) and 2 uL Proteinase K (Promega, Cat # MC5005), then incubated at 65C overnight to reverse crosslinks. DNA was isolated by adding and equal volume of 25:24:1 phenol:chloroform:isoamyl solution, vortexing and centrifuging for 3 minutes at 14,000 rpm, then purifying the top aqueous phase using the MinElute PCR Purification Kit, eluting in 10 uL EB buffer. Transposed DNA was isolated using the MinElute PCR Purification Kit (Qiagen Cat# 28004/28006), and PCR amplified for 10 cycles using the usual ATAC-seq settings. Libraries were purified using the MinElute kit, then sequenced on a Illumina NextSeq 550 instrument as 2x36mers.
Runs: 1 run, 1.8M spots, 140.4M bases, 53.6Mb
Run# of Spots# of BasesSizePublished
SRR199778891,846,807140.4M53.6Mb2022-10-01

ID:
22696447

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