Year: 2024
Type: article
Abstract: Methods to measure chromatin contacts at genomic regions bound by histone modifications or proteins are important tools to investigate chromatin organization. However, such methods do not capture the possible involvement of other epigenomic features such as G-quadruplex DNA secondary structures (G4s). To bridge this gap, we introduce ViCAR (viewpoint HiCAR), for the direct antibody-based capture of chromatin interactions at folded G4s. Through ViCAR, we showcase the first G4-3D interaction landscape. Using histone marks, we also demonstrate how ViCAR improves on earlier approaches yielding increased signal-to-noise. ViCAR is a practical and powerful tool to explore epigenetic marks and 3D genome interactomes.
Source: Genome biology
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $5,290
Awards: To study epigenetic mechanisms regulating lineage commitment and cell potency, G339059223, G3594106981, Higher-order chromatin structure and regulatory sequence variation in human induced pluripotent stem cell (iPSC) self-renewal and differentiation, G4002907240, G5043583218, G5410182794, G63586632, G7064146384, G7101412424, G7471487811, G7567962354, G7887713238, The chemical biology and function of natural modified DNA bases in genomes, G823736304, G8418559812, G8550030593, The chemical biology and function of natural modified DNA bases in genomes
OpenAlex ID: W4402178419
