TY - JOUR
T1 - Boolean Networks with Classic and New Updating Modes Applied to Genetic Regulation in Some Familial Diseases
AU - Demongeot, Jacques
AU - Diallo, Abdoul Khadir
AU - Hazgui, Hana
AU - Jelassi, Mariem
AU - Kelloufi, Fatine
AU - ben Khalfallah, Houssem
AU - Espinoza, Alonso
AU - Montalva-Medel, Marco
N1 - Publisher Copyright:
© 2025 by the authors.
PY - 2025/12
Y1 - 2025/12
N2 - 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.
AB - 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.
KW - Boolean network
KW - biliary atresia
KW - familial angioedema
KW - gene interaction graph
KW - genetic regulatory network
KW - osteogenesis imperfecta
KW - structural robustness
UR - https://www.scopus.com/pages/publications/105025987242
U2 - 10.3390/ijms262411976
DO - 10.3390/ijms262411976
M3 - Article
AN - SCOPUS:105025987242
SN - 1661-6596
VL - 26
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 24
M1 - 11976
ER -