Single-cell absolute contact probability detection reveals that chromosomes are organized by multiple, low-frequency yet specific interactions
D. I. I. Cattoni, A. M. Cardozo Gizzi, M. Georgieva, M. Di Stefano, A. Valeri, D. Chamousset, C. Houbron, S. Dejardin, J.-B. Fiche, I. Gonzalez, J.-M. Chang, T. Sexton, M. A. Marti-Renom, F. Bantignies, G. Cavalli, M. Nollmann
Abstract
At the kilo- to mega-base pair scales, eukaryotic genomes are partitioned into self-interacting modules or topologically associated domains (TADs) that associate to form nuclear compartments. Here, we combined high-content super-resolution microscopies with state-of-the-art DNA labeling methods to reveal the variability in the multiscale organization of the Drosophila genome. We found that association frequencies within TADs and between TAD borders are below ~10%, independently of TAD size, epigenetic state, or cell type. Critically, despite this large heterogeneity, we were able to visualize nanometer-sized epigenetic domains at the single-cell level. In addition, absolute contact frequencies within and between TADs were to a large extent defined by genomic distance, higher-order chromosome architecture, and epigenetic identity. We propose that TADs and compartments are organized by multiple, small frequency, yet specific interactions that are regulated by epigenetics and transcriptional state.
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