Published November 6, 2023 | Version v1
Journal article Open

The chromatin landscape of the euryarchaeon Haloferax volcanii

  • 1. Stanford University
  • 2. University of Chicago

Description

Background: 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, not all archaea possess histones and it is not clear if histones are a main packaging component for all that do. Despite increased interest in archaeal chromatin in recent years, its properties have been little studied using genomic tools.

Results: Here, we adapt the ATAC-seq assay to archaea 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, unlike most eukaryotes, modulation of transcriptional activity is not associated with changes in promoter accessibility. Applying orthogonal single-molecule footprinting methods, we quantify the absolute levels of physical protection of H. volcanii and find that Haloferax chromatin is similarly or only slightly more accessible, in aggregate, 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.

Conclusions: Our results provide the first comprehensive maps of chromatin accessibility and active transcription in Haloferax across conditions and thus a foundation for future functional studies of archaeal chromatin.

Data availability

The sequencing datasets generated for this study can be accessed from GEO accession GSE207470.

Previously published MNase-seq and control datasets for Haloferax were obtained from SRA accesions SRX188663, SRX188665, and SRX185902.

Previously published Sulfolobus ATAC-seq data was downloaded from SRA under project number PRJNA814106. The data processing and visualization code used can be found on GitHub and Zenodo.

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Additional details

Identifiers

DOI
10.1186/s13059-023-03095-5
Other
oai:uchicago.tind.io:9582

Funding

National Institutes of Health
P50HG007735
National Institutes of Health
RO1 HG008140
National Institutes of Health
U19AI057266
National Institutes of Health
UM1HG009442
National Institutes of Health
1UM1HG009436
National Institutes of Health
1DP2OD022870-01
National Institutes of Health
1U01HG009431
Rita Allen Foundation
Baxter Foundation
Faculty Scholar Grant
Human Frontiers Science Program
RGY006S
Chan Zuckerberg Initiative
2017-174468
Chan Zuckerberg Initiative
2018-182817

UChicago Information

Division(s)
Biological Sciences Division, Physical Sciences Division
Department(s)
Biochemistry and Molecular Biology, Chemistry
Center(s) or Institute(s)
Institute for Biophysical Dynamics