Consecutive low-frequency shifts in A/T content denote nucleosome positions across microeukaryotes

Nucleosomes are the basic repeating unit, each spanning ≈150bp, that structures DNA in the nucleus and their positions have major consequences on gene activity. Here, through analyzing DNA signatures across 1117 microeukaryote genomes, we discovered ≈150bp shifts in A/T content associated with nucleosome organization. Often consecutively arrayed across the genome, A/T peaks were enriched surrounding transcriptional start sites in specific clades. Most nucleosomes (both <i>in vitro</i> and <i>in vivo</i>) across eukaryotes aligned with A/T peaks, even in the presence of DNA modifications. Using artificial intelligence-based approaches, we describe DNA features associated with nucleosomes and construct a deep learning (DL) model for improved nucleosome occupancy prediction. Using this model, we found that ≈70% of "random" transfer DNA inserts from an <i>in vivo</i> fungal RB-TDNAseq library avoided DL predicted nucleosome-bound regions. This study reveals a eukaryote-wide strategy for generating cassettes of nucleosome-favorable DNAs that has a profound impact on nucleosome organization.

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Publication Details

Journal
iScience
Published
2025-04-18
DOI
https://doi.org/10.1016/j.isci.2025.112472
Citations
3
Primary Topic
Genomics and Phylogenetic Studies
Type
article
Field-Weighted Citation Impact
2.42

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article

Consecutive low-frequency shifts in A/T content denote nucleosome positions across microeukaryotes

Igor V. Grigoriev, Stephen J. Mondo, M. Catherine Aime, Anna Lipzen et al.
3 citations
iScience
Genomics and Phylogenetic Studies
2.42
article

Consecutive low-frequency shifts in A/T content denote nucleosome positions across microeukaryotes

Igor V. Grigoriev, Stephen J. Mondo, M. Catherine Aime, Anna Lipzen, Ronan C. O’Malley, Lei Shu, Doina Ciobanu, Alan Kuo, Aditi Sharma, Robert Riley, Jon Magnuson, William Andreopoulos, Jasmyn Pangilinan, Kurt LaButti, Guifen He, Asaf Salamov, John Gladden, Hugh Salamon
article en
3 citations

Abstract

Nucleosomes are the basic repeating unit, each spanning ≈150bp, that structures DNA in the nucleus and their positions have major consequences on gene activity. Here, through analyzing DNA signatures across 1117 microeukaryote genomes, we discovered ≈150bp shifts in A/T content associated with nucleosome organization. Often consecutively arrayed across the genome, A/T peaks were enriched surrounding transcriptional start sites in specific clades. Most nucleosomes (both <i>in vitro</i> and <i>in vivo</i>) across eukaryotes aligned with A/T peaks, even in the presence of DNA modifications. Using artificial intelligence-based approaches, we describe DNA features associated with nucleosomes and construct a deep learning (DL) model for improved nucleosome occupancy prediction. Using this model, we found that ≈70% of "random" transfer DNA inserts from an <i>in vivo</i> fungal RB-TDNAseq library avoided DL predicted nucleosome-bound regions. This study reveals a eukaryote-wide strategy for generating cassettes of nucleosome-favorable DNAs that has a profound impact on nucleosome organization.

iScienceVol. 28(5)
Shenyang Agricultural University (CN), Pacific Northwest National Laboratory (US), Lawrence Berkeley National Laboratory (US), Joint Genome Institute (US), Purdue University West Lafayette (US), Ministry of Education and Child Care (CA), Joint BioEnergy Institute (US), Colorado State University (US), University of California, Berkeley (US)
Biological and Environmental Research
Openalex Percentile: Top 12%
Genomics and Phylogenetic Studies
2.42
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