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Identification of chromatin loops from Hi-C interaction matrices by CTCF–CTCF topology classification

Genome-wide profiling of long-range interactions has revealed that the CCCTC-Binding factor (CTCF) often anchors chromatin loops and is enriched at boundaries of the so-called Topologically Associating Domains, which suggests that CTCF is essential in the 3D organization of chromatin. However, the s...

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Detalles Bibliográficos
Autores principales: Galan, Silvia, Serra, François, Marti-Renom, Marc A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903010/
https://www.ncbi.nlm.nih.gov/pubmed/35274099
http://dx.doi.org/10.1093/nargab/lqac021
Descripción
Sumario:Genome-wide profiling of long-range interactions has revealed that the CCCTC-Binding factor (CTCF) often anchors chromatin loops and is enriched at boundaries of the so-called Topologically Associating Domains, which suggests that CTCF is essential in the 3D organization of chromatin. However, the systematic topological classification of pairwise CTCF–CTCF interactions has not been yet explored. Here, we developed a computational pipeline able to classify all CTCF–CTCF pairs according to their chromatin interactions from Hi-C experiments. The interaction profiles of all CTCF–CTCF pairs were further structurally clustered using self-organizing feature maps and their functionality characterized by their epigenetic states. The resulting clusters were then input to a convolutional neural network aiming at the de novo detecting chromatin loops from Hi-C interaction matrices. Our new method, called LOOPbit, is able to automatically detect significant interactions with a higher proportion of enhancer-promoter loops compared to other callers. Our highly specific loop caller adds a new layer of detail to the link between chromatin structure and function.