4.3 Article

The genome organization of Neurospora crassa at high resolution uncovers principles of fungal chromosome topology

Journal

G3-GENES GENOMES GENETICS
Volume 12, Issue 5, Pages -

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/g3journal/jkac053

Keywords

in situ Hi-C; Neurospora; genome organization; genome topology; chromatin

Funding

  1. University of Colorado Colorado Springs (UCCS) College of Letters, Arts, and Sciences
  2. UCCS Committee on Research and Creative Works internal seed grant
  3. Academic Research Enhancement Award (AREA) grant from the National Institutes of Health [1R15GM140396-01]

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The precise organization of the eukaryotic genome is crucial for its proper functioning, and disruptions to genome topology can lead to diseases. High-resolution Hi-C datasets provide valuable insights into the folding principles of individual genes. In this study, the genome topology of the fungal model organism Neurospora crassa is reported, providing valuable insights into higher organism genome topology.
The eukaryotic genome must be precisely organized for its proper function, as genome topology impacts transcriptional regulation, cell division, replication, and repair, among other essential processes. Disruptions to human genome topology can lead to diseases, including cancer. The advent of chromosome conformation capture with high-throughput sequencing (Hi-C) to assess genome organization has revolutionized the study of nuclear genome topology; Hi-C has elucidated numerous genomic structures, including chromosomal territories, active/silent chromatin compartments, Topologically Associated Domains, and chromatin loops. While low-resolution heatmaps can provide important insights into chromosomal level contacts, high-resolution Hi-C datasets are required to reveal folding principles of individual genes. Of particular interest are high-resolution chromosome conformation datasets of organisms modeling the human genome. Here, we report the genome topology of the fungal model organism Neurospora crassa at a high resolution. Our composite Hi-C dataset, which merges 2 independent datasets generated with restriction enzymes that monitor euchromatin (DpnII) and heterochromatin (MseI), along with our DpnII/MseI double digest dataset, provide exquisite detail for both the conformation of entire chromosomes and the folding of chromatin at the resolution of individual genes. Within constitutive heterochromatin, we observe strong yet stochastic internal contacts, while euchromatin enriched with either activating or repressive histone post-translational modifications associates with constitutive heterochromatic regions, suggesting intercompartment contacts form to regulate transcription. Consistent with this, a strain with compromised heterochromatin experiences numerous changes in gene expression. Our high-resolution Neurospora Hi-C datasets are outstanding resources to the fungal community and provide valuable insights into higher organism genome topology.

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