Regulus infers signed regulatory relations from few samples' information using discretization and likelihood constraints.


Journal

PLoS computational biology
ISSN: 1553-7358
Titre abrégé: PLoS Comput Biol
Pays: United States
ID NLM: 101238922

Informations de publication

Date de publication:
22 Jan 2024
Historique:
received: 16 12 2022
accepted: 08 01 2024
medline: 22 1 2024
pubmed: 22 1 2024
entrez: 22 1 2024
Statut: aheadofprint

Résumé

Transcriptional regulation is performed by transcription factors (TF) binding to DNA in context-dependent regulatory regions and determines the activation or inhibition of gene expression. Current methods of transcriptional regulatory circuits inference, based on one or all of TF, regions and genes activity measurements require a large number of samples for ranking the candidate TF-gene regulation relations and rarely predict whether they are activations or inhibitions. We hypothesize that transcriptional regulatory circuits can be inferred from fewer samples by (1) fully integrating information on TF binding, gene expression and regulatory regions accessibility, (2) reducing data complexity and (3) using biology-based likelihood constraints to determine the global consistency between a candidate TF-gene relation and patterns of genes expressions and region activations, as well as qualify regulations as activations or inhibitions. We introduce Regulus, a method which computes TF-gene relations from gene expressions, regulatory region activities and TF binding sites data, together with the genomic locations of all entities. After aggregating gene expressions and region activities into patterns, data are integrated into a RDF (Resource Description Framework) endpoint. A dedicated SPARQL (SPARQL Protocol and RDF Query Language) query retrieves all potential relations between expressed TF and genes involving active regulatory regions. These TF-region-gene relations are then filtered using biological likelihood constraints allowing to qualify them as activation or inhibition. Regulus provides signed relations consistent with public databases and, when applied to biological data, identifies both known and potential new regulators. Regulus is devoted to context-specific transcriptional circuits inference in human settings where samples are scarce and cell populations are closely related, using discretization into patterns and likelihood reasoning to decipher the most robust regulatory relations.

Identifiants

pubmed: 38252636
doi: 10.1371/journal.pcbi.1011816
pii: PCOMPBIOL-D-22-01850
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1011816

Informations de copyright

Copyright: © 2024 Louarn et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Marine Louarn (M)

Univ Rennes, CNRS, Inria, IRISA - UMR 6074, Rennes, France.
UMR_S 1236, Université Rennes 1, INSERM, Etablissement Français du Sang, Rennes, France.

Guillaume Collet (G)

Univ Rennes, CNRS, Inria, IRISA - UMR 6074, Rennes, France.

Ève Barré (È)

Univ Rennes, CNRS, Inria, IRISA - UMR 6074, Rennes, France.

Thierry Fest (T)

UMR_S 1236, Université Rennes 1, INSERM, Etablissement Français du Sang, Rennes, France.
Laboratoire d'Hématologie, Pôle de Biologie, CHU de Rennes, Rennes, France.

Olivier Dameron (O)

Univ Rennes, CNRS, Inria, IRISA - UMR 6074, Rennes, France.

Anne Siegel (A)

Univ Rennes, CNRS, Inria, IRISA - UMR 6074, Rennes, France.

Fabrice Chatonnet (F)

UMR_S 1236, Université Rennes 1, INSERM, Etablissement Français du Sang, Rennes, France.
Laboratoire d'Hématologie, Pôle de Biologie, CHU de Rennes, Rennes, France.

Classifications MeSH