# Complexity reduction by symmetry: Uncovering the minimal regulatory network for logical computation in bacteria

**Authors:** Luis A. Álvarez-García, Wolfram Liebermeister, Ian Leifer, Hernán A. Makse, Stacey Finley, Stacey Finley, Stacey Finley

PMC · DOI: 10.1371/journal.pcbi.1013005 · PLOS Computational Biology · 2025-04-24

## TL;DR

This paper introduces a method to simplify bacterial gene networks using symmetry principles, revealing core circuits responsible for decision-making.

## Contribution

A novel symmetry-based framework, CoReSym, is introduced to reduce gene regulatory networks while preserving dynamics and computational capabilities.

## Key findings

- Gene regulatory networks of E. coli and B. subtilis are reduced to minimal computational cores using symmetry fibrations.
- The core consists of signal vortices with toggle-switches and oscillators that perform memory storage and decision-making.
- This method systematically uncovers the essential structure of biological networks using theoretical symmetry principles.

## Abstract

Symmetry principles play an important role in geometry, and physics, allowing for the reduction of complicated systems to simpler, more comprehensible models that preserve the system’s features of interest. Biological systems are often highly complex and may consist of a large number of interacting parts. Using symmetry fibrations, the relevant symmetries for biological “message-passing” networks, we introduce a scheme, called Complexity Reduction by Symmetry or CoReSym, to reduce the gene regulatory networks of Escherichia coli and Bacillus subtilis bacteria to core networks in a way that preserves the dynamics and uncovers the computational capabilities of the network. Gene nodes in the original network that share isomorphic input trees are collapsed by the fibration into equivalence classes called fibers, whereby nodes that receive signals with the same “history” belong to one fiber and synchronize. Then we reduce the networks to its minimal computational core via k-core decomposition. This computational core consists of a few strongly connected components or “signal vortices,” in which signals can cycle through. While between them, these “signal vortices” transmit signals in a feedforward manner. These connected components perform signal processing and decision making in the bacterial cell by employing a series of genetic toggle-switch circuits that store memory, plus oscillator circuits. These circuits act as the central computation device of the network, whose output signals then spread to the rest of the network. Our reduction method opens the door to narrow the vast complexity of biological systems to their minimal parts in a systematic way by using fundamental theoretical principles of symmetry.

Biological systems are constituted by complex interactions between a large number of different components, and being able to reduce their complexity in order to understand their behavior is of paramount importance. Here we use symmetry principles, in a manner akin to physics, to reduce the Gene Regulatory Networks (GRN) of Escherichia coli and Bacillus subtilis bacteria to reveal the computational core structure of these networks responsible for driving their dynamics. This computational core comprises gene logic circuits, such as toggle-switches and oscillatory circuits, which ultimately are in charge of the decision making in the bacterial cell. This Complexity Reduction by Symmetries (CoReSym) method opens the way to understanding biological complexity based on firm theoretical principles.

## Linked entities

- **Species:** Escherichia coli (taxon 562), Bacillus subtilis (taxon 1423)

## Full-text entities

- **Species:** Escherichia coli (E. coli, species) [taxon 562], Bacillus subtilis (species) [taxon 1423]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12048163/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12048163/full.md

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Source: https://tomesphere.com/paper/PMC12048163