Benefiting from the intrinsic role of epigenetics to predict patterns of CTCF binding

Villaman, Camilo; Pollastri, Gianluca; SAEZ-VENEGAS, MAURICIO ALEJANDRO; Martin, Alberto J.

Abstract

Motivation: One of the most relevant mechanisms involved in the determination of chromatin structure is the formation of structural loops that are also related with the conservation of chromatin states. Many of these loops are stabilized by CCCTC-binding factor (CTCF) proteins at their base. Despite the relevance of chromatin structure and the key role of CTCF, the role of the epigenetic factors that are involved in the regulation of CTCF binding, and thus, in the formation of structural loops in the chromatin, is not thoroughly understood.Results: Here we describe a CTCF binding predictor based on Random Forest that employs different epigenetic data and genomic features. Importantly, given the ability of Random Forests to determine the relevance of features for the prediction, our approach also shows how the different types of descriptors impact the binding of CTCF, confirming previous knowledge on the relevance of chromatin accessibility and DNA methylation, but demonstrating the effect of epigenetic modifications on the activity of CTCF. We compared our approach against other predictors and found improved performance in terms of areas under PR and ROC curves (PRAUC-ROCAUC), outperforming current state-of-the-art methods. (c) 2023 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Más información

Título según WOS: Benefiting from the intrinsic role of epigenetics to predict patterns of CTCF binding
Título según SCOPUS: ID SCOPUS_ID:85160015780 Not found in local SCOPUS DB
Título de la Revista: Computational and Structural Biotechnology Journal
Volumen: 21
Fecha de publicación: 2023
Página de inicio: 3024
Página final: 3031
DOI:

10.1016/J.CSBJ.2023.05.012

Notas: ISI, SCOPUS