| Literature DB >> 31011212 |
Jonas Paulsen1, Tharvesh M Liyakat Ali1, Maxim Nekrasov2,3, Erwan Delbarre1, Marie-Odile Baudement1, Sebastian Kurscheid2, David Tremethick4, Philippe Collas5,6.
Abstract
Genomic information is selectively used to direct spatial and temporal gene expression during differentiation. Interactions between topologically associating domains (TADs) and between chromatin and the nuclear lamina organize and position chromosomes in the nucleus. However, how these genomic organizers together shape genome architecture is unclear. Here, using a dual-lineage differentiation system, we report long-range TAD-TAD interactions that form constitutive and variable TAD cliques. A differentiation-coupled relationship between TAD cliques and lamina-associated domains suggests that TAD cliques stabilize heterochromatin at the nuclear periphery. We also provide evidence of dynamic TAD cliques during mouse embryonic stem-cell differentiation and somatic cell reprogramming and of inter-TAD associations in single-cell high-resolution chromosome conformation capture (Hi-C) data. TAD cliques represent a level of four-dimensional genome conformation that reinforces the silencing of repressed developmental genes.Entities:
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Year: 2019 PMID: 31011212 DOI: 10.1038/s41588-019-0392-0
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330