Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions
By Zhihu Zhao, Gholamreza Tavoosidana, M. Sjölinder, A. Göndör, P. Mariano, Sha Wang, C. Kanduri, M. Lezcano, K. Sandhu, Umashankar Singh and 4 more. Nature Genetics, 2006
990 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/e3746c669be7f40d37d36b29efa4d5cd8cf5d08b
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Citations in the corpus
- Hi-C: A comprehensive technique to capture the conformation of genomes (2012, methodology): “In recent years, new approaches such as 4C, 5C, and Hi-C have been developed to utilize Next Generation Sequencing (NGS) technologies in order to interrogate the 3C ligation product library more comprehensively (figure 1D and 1E) [7-10].”
- CTCF: Master Weaver of the Genome (2009, positive): “For example, at the H19/Igf2 ICR all four CTCF-binding sites are regulated by methylation to control allele-specific CTCF occupancy and subsequent loop formation.”
- Beyond the sequence: cellular organization of genome function. (2007, positive): “…of methods to probe the physical association of genome regions in a unbiased and genome-wide scale should lead to rapid progress in our still-rudimentary understanding of the functional significance of chromatin loops (Simonis et al., 2006; Wurtele and Chartrand, 2006; Zhao et al., 2006).”
- Chromosome territories. (2010, methodology): “…of specific genomic loci is the technique of “chromosome conformation capture” (3C) introduced by Dekker et al. (2002) and its recent extension to 4C (chromosome conformation capture-on-chip [Simonis et al. 2006] and “circular chromosome conformation capture” [Zhao et al. 2006]), respectively.”
- Architectural protein subclasses shape 3D organization of genomes during lineage commitment. (2013, neutral): “…molecular methods based on proximity ligation, such as chromosome conformation capture (3C) or circularized-3C (4C), have been used to detect functional long-range interactions between two specific genomic loci in a population of cells (Dekker et al., 2002; Simonis et al., 2006; Zhao et al., 2006).”
- Roles, Functions, and Mechanisms of Long Non-coding RNAs in Cancer (2016, background): “More recent technical developments have focused on higher-throughput analyses and these include circular chromosome conformation capture (4C) [66,67], chromosome conformation capture carbon copy (5C) [68], combined 3C-ChIP-cloning (6C) [69], chromatin interaction analysis with paired-end tag sequenc”
- Genome-wide mapping and analysis of chromosome architecture (2016, methodology): “…using 4C (circular chromosome conformation capture; also known as chromosome conformation capture-on-chip) technology, as 4C interrogates the chromatin looping landscape of only a single restriction fragment with the rest of the genome, rather than all possible pairwise contacts genome-wide 45,46 .”
- CTCF-Mediated Functional Chromatin Interactome in Pluripotent Cells (2011, methodology): “Beyond these well-characterized interactions, additional CTCF-dependent inter- and intrachromosomal interactions were identified from these imprinting regions using circular chromosome conformation capture (4C”
- Exploring the three-dimensional organization of genomes: interpreting chromatin interaction data (2013, positive): “4C (also known as ‘circular 3C’ or ‘3C‑on‑chip’) uses inverse PCR to generate genome‑wide interaction profiles for single loci 48,105,106 .”
- Epigenetic modifications and human disease (2010, background): “These physical interactions in trans can regulate transcription, as shown for the H19 imprinting control region and the Osbpl1a/Impact loc”
- Functional and mechanistic diversity of distal transcription enhancers (2011, positive): “This approach has been adapted to produce genome-wide maps of the threedimensional associations that a specific locus makes among all of the other sequences in the genome (‘‘4C’’) (Zhao et al., 2006; Simonis et al., 2006) or even associations among multiple sequences located throughout the genome (‘”
- A decade of 3C technologies: insights into nuclear organization. (2012, background): “In mammals, CTCF sites form chromatin loops by contacting each other in the b-globin locus (Splinter et al. 2006) and H19/Igf2 locus (Zhao et al. 2006).”