Boolean Networks with Classic and New Updating Modes Applied to Genetic Regulation in Some Familial Diseases

Many familial diseases are caused by genetic accidents, which affect the genome and its epigenetic environment, summarized as an interaction network between genes. We wish to study the existence or absence of robustness for such genetic interaction networks centered on the gene SP1 and involved in three familial diseases: familial angioedema, osteogenesis imperfecta, and biliary atresia. The updating of gene states at the vertices of the interaction graph of the genetic network (1 if a gene is activated, 0 if it is inhibited) can be performed in multiple ways that have been well-studied over the last 20 years: parallel, block-parallel, sequential, block-sequential, random, etc. We add to these classic updating modes two new ones, the intricate and the state-dependent. We have studied the robustness of three particular interaction graphs related to the familial diseases chosen as examples. The comparison of the interaction graphs and dynamics of the chosen familial diseases of different etiology shows common points in their interaction graphs and similarities in their dynamics according to their expression clock.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-12-12
DOI
https://doi.org/10.3390/ijms262411976
Primary Topic
Kruppel-like factors research
Type
article
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article

Boolean Networks with Classic and New Updating Modes Applied to Genetic Regulation in Some Familial Diseases

Marco Montalva-Medel, Adama Diallo, Jacques Demongeot, Houssem Ben Khalfallah et al.
International Journal of Molecular Sciences
Kruppel-like factors research
article

Boolean Networks with Classic and New Updating Modes Applied to Genetic Regulation in Some Familial Diseases

Marco Montalva-Medel, Adama Diallo, Jacques Demongeot, Houssem Ben Khalfallah, Alonso Espinoza, Hana Hazgui, Fatine Kelloufi
article en

Abstract

Many familial diseases are caused by genetic accidents, which affect the genome and its epigenetic environment, summarized as an interaction network between genes. We wish to study the existence or absence of robustness for such genetic interaction networks centered on the gene SP1 and involved in three familial diseases: familial angioedema, osteogenesis imperfecta, and biliary atresia. The updating of gene states at the vertices of the interaction graph of the genetic network (1 if a gene is activated, 0 if it is inhibited) can be performed in multiple ways that have been well-studied over the last 20 years: parallel, block-parallel, sequential, block-sequential, random, etc. We add to these classic updating modes two new ones, the intricate and the state-dependent. We have studied the robustness of three particular interaction graphs related to the familial diseases chosen as examples. The comparison of the interaction graphs and dynamics of the chosen familial diseases of different etiology shows common points in their interaction graphs and similarities in their dynamics according to their expression clock.

International Journal of Molecular SciencesVol. 26(24)
Adolfo Ibáñez University (CL), Aix-Marseille Université (FR), Manouba University (TN), Université Grenoble Alpes (FR)
Openalex Percentile: Top 64%
Kruppel-like factors research
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