Evidence map›Paper›PMID 40273291›Full record

ArticlePLoS computational biology2025

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

Luis A Álvarez-García, Wolfram Liebermeister, Ian Leifer, Hernán A Makse

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Luis A Álvarez-GarcíaLevich Institute and Physics Department, City College of New York, New York, New York 10031, United States of America.ORCID 0009-0008-0229-2461
Wolfram LiebermeisterUniversité Paris-Saclay, INRAE, MaIAGE, 78350 Jouy-en-Josas, France.ORCID 0000-0002-2568-2381
Ian LeiferLevich Institute and Physics Department, City College of New York, New York, New York 10031, United States of America.
Hernán A MakseLevich Institute and Physics Department, City College of New York, New York, New York 10031, United States of America.

Funding

Application of the principle of symmetry to neural circuitry: From building blocks to neural synchronization in the connectomeR01EB028157 · NIBIB · CITY COLLEGE OF NEW YORK · PI MAKSE, HERNAN, ZIMMER, MANUEL · 2020 to 2020
$1.1M
NIBIB NIH HHS R01 EB028157
6 · The paper itself

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.

Indexed as

Bacillus subtilisComputational BiologyGene Regulatory NetworksModels, BiologicalAlgorithmsComputer SimulationEscherichia coliGene Expression Regulation, BacterialSignal Transduction

Identifiers

PMID40273291
PMCPMC12048163

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.