bioRxivGenomicsPreprint
Re-configuration of Chromatin Structure During the Mitosis-G1 Phase Transition
Haoyue ZhangiD, Daniel J. EmersoniD, Thomas G. Gilgenast, Katelyn R. TitusiD, Yemin LaniD, Peng HuangiD, Di ZhangiD, Hongxin WangiD, Cheryl A. KelleriD, Belinda M. GiardineiD, Ross C. HardisoniD, Jennifer E. Phillips‐CreminsiD, Gerd A. BlobeliD
Abstract
Higher-order chromatin organization such as A/B compartments, TADs and chromatin loops are temporarily disrupted during mitosis. These structures are thought to organize aspects of gene regulation, and thus it is important to understand how they are re-established after mitosis. We examined the dynamics of chromosome reorganization by Hi-C at defined time points following exit from mitosis in highly purified, synchronous cell populations. We observed that A/B compartments are rapidly established and progressively gain in strength following mitotic exit. Contact domain formation occurs from the \"bottom-up\" with smaller sub-TADs forming initially, followed by convergence into multi-domain TAD structures. CTCF is strongly retained at a significant fraction of sites on mitotic chromosomes and immediately resumes full binding at ana/telophase, the earliest tested time point. In contrast, cohesin is completely evicted from mitotic chromosomes and resumes focal binding with delayed kinetics. The formation of CTCF/cohesin co-anchored structural loops follows the kinetics of cohesin positioning. Stripe-shaped contacts anchored by CTCF grow in length, consistent with a loop extrusion process after mitosis. Interactions between cis-regulatory elements can form rapidly, preceding CTCF/cohesin anchored structural loops. Strikingly, we identified a group of rapidly emerging transient contacts between cis-regulatory elements in ana/telophase, that are dissolved upon G1 entry, co-incident with the establishment of inner boundaries or nearby interfering loops. Our findings indicate that distinct but mutually influential forces drive post-mitotic chromatin re-configuration to shape compartments, contact domains, cis-element contacts, and CTCF/cohesin dependent loops.
- organism: human
- assay: Hi-C
- research focus: gene regulatory network inference
- research focus: spatial domain detection
- approach: statistical model
- Citations
- 6
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