Informational blueprints reveal condition-dependent gene regulatory architectures

Fuente: arXiv
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Hauptverfasser: Gökmen, Doruk Efe, Pan, Rosalind Wenshan, Röschinger, Tom, Quake, Stephen, Garcia, Hernan, Phillips, Rob, Vitelli, Vincenzo
Format: Preprint
Veröffentlicht: 2026
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author Gökmen, Doruk Efe
Pan, Rosalind Wenshan
Röschinger, Tom
Quake, Stephen
Garcia, Hernan
Phillips, Rob
Vitelli, Vincenzo
author_facet Gökmen, Doruk Efe
Pan, Rosalind Wenshan
Röschinger, Tom
Quake, Stephen
Garcia, Hernan
Phillips, Rob
Vitelli, Vincenzo
contents While coding regions in the genome have a direct interpretation in terms of protein products, significant fractions are non-coding and yet control essential biological functions. Unlike the genetic code, there is no "lookup table" that identifies where regulatory proteins, known as transcription factors (TFs), bind. Here, we extract these binding sites by distilling sequences of nucleotide letters into collective coordinates (hyperletters) representing the binding sites that are active under specific environmental conditions. Going beyond local information footprints between individual bases and expression levels, our $\textit{information blueprint}$ algorithm compresses the global information by optimising filters that simultaneously scan an entire promoter sequence. Inspired by renormalisation-group techniques, we identify TF binding sites as coarse-grained variables combining groups of correlated mutations with the highest collective impact on gene expression. We validate our approach on experimental data for $\textit{E. coli}$ and discover novel regulatory elements illustrating its deployment at scale across growth conditions.
format Preprint
id arxiv_https___arxiv_org_abs_2605_19071
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Informational blueprints reveal condition-dependent gene regulatory architectures
Gökmen, Doruk Efe
Pan, Rosalind Wenshan
Röschinger, Tom
Quake, Stephen
Garcia, Hernan
Phillips, Rob
Vitelli, Vincenzo
Genomics
Statistical Mechanics
Molecular Networks
Quantitative Methods
While coding regions in the genome have a direct interpretation in terms of protein products, significant fractions are non-coding and yet control essential biological functions. Unlike the genetic code, there is no "lookup table" that identifies where regulatory proteins, known as transcription factors (TFs), bind. Here, we extract these binding sites by distilling sequences of nucleotide letters into collective coordinates (hyperletters) representing the binding sites that are active under specific environmental conditions. Going beyond local information footprints between individual bases and expression levels, our $\textit{information blueprint}$ algorithm compresses the global information by optimising filters that simultaneously scan an entire promoter sequence. Inspired by renormalisation-group techniques, we identify TF binding sites as coarse-grained variables combining groups of correlated mutations with the highest collective impact on gene expression. We validate our approach on experimental data for $\textit{E. coli}$ and discover novel regulatory elements illustrating its deployment at scale across growth conditions.
title Informational blueprints reveal condition-dependent gene regulatory architectures
topic Genomics
Statistical Mechanics
Molecular Networks
Quantitative Methods
url https://arxiv.org/abs/2605.19071