Type II topoisomerases shape multi-scale 3D chromatin folding in regions of positive supercoils
Year: 2024
Type: article
Abstract: Type II topoisomerases (TOP2s) resolve torsional stress accumulated during various cellular processes and are enriched at chromatin loop anchors and topologically associated domain (TAD) boundaries, where, when trapped, can lead to genomic instability promoting the formation of oncogenic fusions. Whether TOP2s relieve topological constraints at these positions and/or participate in 3D chromosome folding remains unclear. Here, we combine 3D genomics, imaging, and GapRUN, a method for the genome-wide profiling of positive supercoiling, to assess the role of TOP2s in shaping chromosome organization in human cells. Acute TOP2 depletion led to the emergence of new, large-scale contacts at the boundaries between active, positively supercoiled, and lamina-associated domains. TOP2-dependent changes at the higher-order chromatin folding were accompanied by remodeling of chromatin-nuclear lamina interactions and of gene expression, while at the chromatin loop level, TOP2 depletion predominantly remodeled transcriptionally anchored, positively supercoiled loops. We propose that TOP2s act as a fine regulator of chromosome folding at multiple scales.
Source: Molecular Cell
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $9,350
Awards: SPP 2202: 3DGenomarchitektur in Entwicklung und Krankheit, G2121096491, Erforschung des Beitrags von RNAPolymerasen zur 3DGenomarchitektur von Säugetieren, SFB 1361: Regulation von DNAReparatur und Genomstabilität, G3375785483, G5302157289, G5860385120, Untersuchung der Rolle menschlicher Topoisomerasen bei der Aufrechterhaltung der Chromosomentopologie und der Verhinderung genomischer Instabilität
OpenAlex ID: W4403926089
