Gauge fixing for sequence-function relationships

Quantitative models of sequence-function relationships are ubiquitous in computational biology, e.g., for modeling the DNA binding of transcription factors or the fitness landscapes of proteins. Interpreting these models, however, is complicated by the fact that the values of model parameters can often be changed without affecting model predictions. Before the values of model parameters can be meaningfully interpreted, one must remove these degrees of freedom (called "gauge freedoms" in physics) by imposing additional constraints (a process called "fixing the gauge"). However, strategies for fixing the gauge of sequence-function relationships have received little attention. Here we derive an analytically tractable family of gauges for a large class of sequence-function relationships. These gauges are derived in the context of models with all-order interactions, but an important subset of these gauges can be applied to diverse types of models, including additive models, pairwise-interaction models, and models with higher-order interactions. Many commonly used gauges are special cases of gauges within this family. We demonstrate the utility of this family of gauges by showing how different choices of gauge can be used both to explore complex activity landscapes and to reveal simplified models that are approximately correct within localized regions of sequence space. The results provide practical gauge-fixing strategies and demonstrate the utility of gauge-fixing for model exploration and interpretation.

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Publication Details

Journal
PLoS Computational Biology
Published
2025-03-20
DOI
https://doi.org/10.1371/journal.pcbi.1012818
Citations
7
Primary Topic
Evolution and Genetic Dynamics
Type
article
Field-Weighted Citation Impact
12.72

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article

Gauge fixing for sequence-function relationships

David M. McCandlish, Anna Posfai, Justin B. Kinney, Juannan Zhou
7 citations
PLoS Computational Biology
Evolution and Genetic Dynamics
12.72
article

Gauge fixing for sequence-function relationships

David M. McCandlish, Anna Posfai, Justin B. Kinney, Juannan Zhou
article en
7 citations

Abstract

Quantitative models of sequence-function relationships are ubiquitous in computational biology, e.g., for modeling the DNA binding of transcription factors or the fitness landscapes of proteins. Interpreting these models, however, is complicated by the fact that the values of model parameters can often be changed without affecting model predictions. Before the values of model parameters can be meaningfully interpreted, one must remove these degrees of freedom (called "gauge freedoms" in physics) by imposing additional constraints (a process called "fixing the gauge"). However, strategies for fixing the gauge of sequence-function relationships have received little attention. Here we derive an analytically tractable family of gauges for a large class of sequence-function relationships. These gauges are derived in the context of models with all-order interactions, but an important subset of these gauges can be applied to diverse types of models, including additive models, pairwise-interaction models, and models with higher-order interactions. Many commonly used gauges are special cases of gauges within this family. We demonstrate the utility of this family of gauges by showing how different choices of gauge can be used both to explore complex activity landscapes and to reveal simplified models that are approximately correct within localized regions of sequence space. The results provide practical gauge-fixing strategies and demonstrate the utility of gauge-fixing for model exploration and interpretation.

PLoS Computational BiologyVol. 21(3)
Cold Spring Harbor Laboratory (US), University of Florida (US)
Alfred P. Sloan Foundation, National Institutes of Health, College of Liberal Arts and Sciences, University of Florida, National Institute of General Medical Sciences
Peace, Justice and strong institutions
Openalex Percentile: Top 1%
Evolution and Genetic Dynamics
12.72
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