Predicting synchronized gene coexpression patterns from fibration symmetries in gene regulatory networks in bacteria


Por: Leifer, Ian, Sanchez-Perez, Mishael, Ishida, Cecilia, Makse, Hernan A.

Publicada: 8 jul 2021
Resumen:
Background: Gene regulatory networks coordinate the expression of genes across physiological states and ensure a synchronized expression of genes in cellular subsystems, critical for the coherent functioning of cells. Here we address the question whether it is possible to predict gene synchronization from network structure alone. We have recently shown that synchronized gene expression can be predicted from symmetries in the gene regulatory networks described by the concept of symmetry fibrations. We showed that symmetry fibrations partition the genes into groups called fibers based on the symmetries of their `input trees', the set of paths in the network through which signals can reach a gene. In idealized dynamic gene expression models, all genes in a fiber are perfectly synchronized, while less idealized models-with gene input functions differencing between genes-predict symmetry breaking and desynchronization. Results: To study the functional role of gene fibers and to test whether some of the fiber-induced coexpression remains in reality, we analyze gene fibrations for the gene regulatory networks of E. coli and B. subtilis and confront them with expression data. We find approximate gene coexpression patterns consistent with symmetry fibrations with idealized gene expression dynamics. This shows that network structure alone provides useful information about gene synchronization, and suggest that gene input functions within fibers may be further streamlined by evolutionary pressures to realize a coexpression of genes. Conclusions: Thus, gene fibrations provide a sound conceptual tool to describe tunable coexpression induced by network topology and shaped by mechanistic details of gene expression.

Filiaciones:
CUNY City Coll, Dept Phys, Levich Inst, New York, NY 10031 USA
Univ Nacl Autonoma Mexico, Programa Genom Computac, Ctr Ciencias Genom, Cuernavaca, Morelos, Mexico
Autonomous Univ Chihuahua, Fac Med & Biomed Sci, Chihuahua 31125, Chihuahua, Mexico
ISSN: 14712105





Bmc Bioinformatics
Editorial
BIOMED CENTRAL LTD, CURRENT SCIENCE GROUP, MIDDLESEX HOUSE, 34-42 CLEVELAND ST, LONDON W1T 4LB, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 22 Número: 1
Páginas:
WOS Id: 000672672200001
ID de PubMed: 34238210
imagen Green Published, Green Submitted, gold

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