: Cells regulate gene expression by balancing transcriptional resources across different functional groups of genes. In Escherichia coli, second messengers such as ppGpp and cAMP control ribosome biogenesis and metabolic gene expression, respectively. While these regulators are typically studied in isolation, we provide a theory showing that their effects are intertwined as a result of global transcriptional competition. Using experimental data from RelA overexpression and a mechanistic modeling framework, we show that ppGpp-mediated repression of ribosomal genes competes for transcriptional resources with cAMP-driven activation of catabolic genes. This competition reshapes proteome allocation in a way that transcends individual regulators. Our findings challenge common modeling assumptions about transcription factor action and revive classical ideas suggesting that large-scale gene regulation should be studied within the broader context of resource availability, with implications for understanding cellular regulation across diverse biological systems beyond bacterial physiology.
Transcriptional competition biases the effects of second messengers in Escherichia coli / A. Ripamonti, M. Lacassin, R. Droghetti, G. Bokinsky, M. Cosentino Lagomarsino. - In: CELL SYSTEMS. - ISSN 2405-4712. - (2026). [Epub ahead of print] [10.1016/j.cels.2026.101609]
Transcriptional competition biases the effects of second messengers in Escherichia coli
R. Droghetti;M. Cosentino Lagomarsino
Ultimo
2026
Abstract
: Cells regulate gene expression by balancing transcriptional resources across different functional groups of genes. In Escherichia coli, second messengers such as ppGpp and cAMP control ribosome biogenesis and metabolic gene expression, respectively. While these regulators are typically studied in isolation, we provide a theory showing that their effects are intertwined as a result of global transcriptional competition. Using experimental data from RelA overexpression and a mechanistic modeling framework, we show that ppGpp-mediated repression of ribosomal genes competes for transcriptional resources with cAMP-driven activation of catabolic genes. This competition reshapes proteome allocation in a way that transcends individual regulators. Our findings challenge common modeling assumptions about transcription factor action and revive classical ideas suggesting that large-scale gene regulation should be studied within the broader context of resource availability, with implications for understanding cellular regulation across diverse biological systems beyond bacterial physiology.| File | Dimensione | Formato | |
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