Publication

Comprehensive mapping of long-range interactions reveals folding principles of the human genome.

current
   March 28th, 2019 at 3:01pm

Overview


Abstract

We describe Hi-C, a method that probes the three-dimensional architecture of whole genomes by coupling proximity-based ligation with massively parallel sequencing. We constructed spatial proximity maps of the human genome with Hi-C at a resolution of 1 megabase. These maps confirm the presence of chromosome territories and the spatial proximity of small, gene-rich chromosomes. We identified an additional level of genome organization that is characterized by the spatial segregation of open and closed chromatin to form two genome-wide compartments. At the megabase scale, the chromatin conformation is consistent with a fractal globule, a knot-free, polymer conformation that enables maximally dense packing while preserving the ability to easily fold and unfold any genomic locus. The fractal globule is distinct from the more commonly used globular equilibrium model. Our results demonstrate the power of Hi-C to map the dynamic conformations of whole genomes.

Authors

Lieberman-Aiden E  •  van Berkum NL  •  Williams L  •  Imakaev M  •  Ragoczy T  •  Telling A  •  Amit I  •  Lajoie BR  •  Sabo PJ  •  Dorschner MO  •  Sandstrom R  •  Bernstein B  •  Bender MA  •  Groudine M  •  Gnirke A  •  Stamatoyannopoulos J  •  Mirny LA  •  Lander ES  •  Dekker J

Link

https://www.ncbi.nlm.nih.gov/pubmed/19815776


Journal

Science (New York, N.Y.)

doi:10.1126/science.1181369

Published

October 9th, 2009