Hi-C: A comprehensive technique to capture the conformation of genomes
Program in Systems Biology; Program in Gene Function and Expression; Department of Biochemistry and Molecular Pharmacology
Chromatin; Chromosomes; Genomics; Cell Nucleus
Genetics and Genomics
We describe a method, Hi-C, to comprehensively detect chromatin interactions in the mammalian nucleus. This method is based on chromosome conformation capture, in that chromatin is crosslinked with formaldehyde, then digested, and re-ligated in such a way that only DNA fragments that are covalently linked together form ligation products. The ligation products contain the information of not only where they originated from in the genomic sequence but also where they reside, physically, in the 3D organization of the genome. In Hi-C, a biotin-labeled nucleotide is incorporated at the ligation junction, enabling selective purification of chimeric DNA ligation junctions followed by deep sequencing. The compatibility of Hi-C with next generation sequencing platforms makes it possible to detect chromatin interactions on an unprecedented scale. This advance gives Hi-C the power to both explore the biophysical properties of chromatin as well as the implications of chromatin structure for the biological functions of the nucleus. A massively parallel survey of chromatin interaction provides the previously missing dimension of spatial context to other genomic studies. This spatial context will provide a new perspective to studies of chromatin and its role in genome regulation in normal conditions and in disease.
DOI of Published Version
Methods. 2012 May 29. Link to article on publisher's site
Methods (San Diego, Calif.)
Belton, Jon-Matthew; McCord, Rachel Patton; Gibcus, Johan H.; Naumova, Natalia; Zhan, Ye; and Dekker, Job, "Hi-C: A comprehensive technique to capture the conformation of genomes" (2012). Program in Gene Function and Expression Publications and Presentations. 198.