» Articles » PMID: 18265379

Mapping Chromatin Interactions by Chromosome Conformation Capture

Overview
Specialty Molecular Biology
Date 2008 Feb 12
PMID 18265379
Citations 67
Authors
Affiliations
Soon will be listed here.
Abstract

Chromosome conformation capture (3C) is one of the only techniques that allows for analysis of an intermediate level of chromosome structure ranging from a few to hundreds of kilobases, a level most relevant for gene regulation. The 3C technique is used to detect physical interactions between sequence elements that are located on the same or on different chromosomes. For instance, physical interactions between distant enhancers and target genes can be measured. The 3C assay uses formaldehyde cross-linking to trap connections between chromatin segments that can, after a number of manipulations, be detected by PCR. This unit describes detailed protocols for performing 3C with yeast Saccharomyces cerevisiae and mammalian cells.

Citing Articles

A biallelically active embryonic enhancer dictates GNAS imprinting through allele-specific conformations.

Iwasaki Y, Reyes M, Juppner H, Bastepe M Nat Commun. 2025; 16(1):1377.

PMID: 39910084 PMC: 11799514. DOI: 10.1038/s41467-025-56608-0.


Genome-wide analysis of the interplay between chromatin-associated RNA and 3D genome organization in human cells.

Calandrelli R, Wen X, Charles Richard J, Luo Z, Nguyen T, Chen C Nat Commun. 2023; 14(1):6519.

PMID: 37845234 PMC: 10579264. DOI: 10.1038/s41467-023-42274-7.


Regulatory architecture of housekeeping genes is driven by promoter assemblies.

Dejosez M, DallAgnese A, Ramamoorthy M, Platt J, Yin X, Hogan M Cell Rep. 2023; 42(5):112505.

PMID: 37182209 PMC: 10329844. DOI: 10.1016/j.celrep.2023.112505.


The long-range interaction between two GNAS imprinting control regions delineates pseudohypoparathyroidism type 1B pathogenesis.

Iwasaki Y, Aksu C, Reyes M, Ay B, He Q, Bastepe M J Clin Invest. 2023; 133(8).

PMID: 36853809 PMC: 10104902. DOI: 10.1172/JCI167953.


Disruption of c-MYC Binding and Chromosomal Looping Involving Genetic Variants Associated With Ankylosing Spondylitis Upstream of the Promoter.

Cohen C, Davidson C, Selmi C, Bowness P, Knight J, Wordsworth B Front Genet. 2022; 12:741867.

PMID: 35069677 PMC: 8782160. DOI: 10.3389/fgene.2021.741867.