Author:
Meng Luming,Sheong Fu Kit,Luo Qiong
Abstract
SUMMARYTopologically associating domains (TADs) are critical for gene regulation. Current views attribute TAD formation to cohesin-mediated extrusion and ignore the role of physical properties ofin vivochromatin. Here, we demonstrate that the two universal properties: chromatin fluidlike behavior and heterogeneity in DNA-packing density along chromatin, can drive TAD formation. We use DNA-accessibility data to parameterize DNA-packing density along chromatin and simulate stochastic folding of the heterogeneous chromatin in nucleus to yield a conformation ensemble. Such an ensemble can be cross-validated by Hi-C and FISH data. Furthermore, the stochastic folding model allowsde novoprediction of the establishment and disappearance of key TADs during early T cell differentiation. Together, our work demonstrates that the intrinsic stochastic folding of fluidlike chromatin leads to the prevalence of TAD-like domains in single cells and their cell-to-cell variation, while the heterogeneity in DNA-packing density along chromatin mediates the emergence of TADs at ensemble-averaged level.In briefA study based on polymer simulation reveals that the two universal physical properties ofin vivochromatin fiber: chromatin fluidlike behavior and heterogeneity in DNA-packing density along chromatin play a vital role in TAD formation.HighlightsIntrinsic stochastic folding of fluidlike chromatin in nuclear space underlies the prevalence of TAD-like domains in single cells and their cell-to-cell variationHeterogeneity in DNA-packing density along chromatin causes the emergence of TADs at ensemble-averaged levelThe disappearance and establishment of key TADs during early T cell differentiation can occur through a stochastic folding process alone, without the need of any cohesin-mediated chromatin extrusionThe stochastic folding model applies to diverse cell types and is thus able tode novopredict the dynamics of genome organization over time
Publisher
Cold Spring Harbor Laboratory