Single-allele chromatin interactions identify regulatory hubs in dynamic compartmentalized domains
Program in Systems Biology, Department of Biochemistry and Molecular Pharmacology
Amino Acids, Peptides, and Proteins | Cells | Computational Biology | Genetic Phenomena | Molecular Biology | Structural Biology | Systems Biology
The promoters of mammalian genes are commonly regulated by multiple distal enhancers, which physically interact within discrete chromatin domains. How such domains form and how the regulatory elements within them interact in single cells is not understood. To address this we developed Tri-C, a new chromosome conformation capture (3C) approach, to characterize concurrent chromatin interactions at individual alleles. Analysis by Tri-C identifies heterogeneous patterns of single-allele interactions between CTCF boundary elements, indicating that the formation of chromatin domains likely results from a dynamic process. Within these domains, we observe specific higher-order structures that involve simultaneous interactions between multiple enhancers and promoters. Such regulatory hubs provide a structural basis for understanding how multiple cis-regulatory elements act together to establish robust regulation of gene expression.
DOI of Published Version
Nat Genet. 2018 Dec;50(12):1744-1751. doi: 10.1038/s41588-018-0253-2. Epub 2018 Oct 29. Link to article on publisher's site
Oudelaar AM, Davies JO, Hanssen LL, Telenius JM, Schwessinger R, Liu Y, Brown JM, Downes DJ, Chiariello AM, Bianco S, Nicodemi M, Buckle VJ, Dekker J, Higgs DR, Hughes JR. (2018). Single-allele chromatin interactions identify regulatory hubs in dynamic compartmentalized domains. Program in Systems Biology Publications and Presentations. https://doi.org/10.1038/s41588-018-0253-2. Retrieved from https://escholarship.umassmed.edu/sysbio_pubs/152