arXiv subjects

Benjamin Zoller

Publications and source records attributed to Benjamin Zoller.

4 recordsLinked to original sources

arXiv2025

Invariant non-equilibrium dynamics of transcriptional regulation optimize information flow

Eukaryotic gene regulation is based on stochastic yet controlled promoter switching, during which genes transition between transcriptionally active and inactive states. Despite the molecular complexity of this process, recent studies reveal a surprising invariance of the "switching correlation time" ($T_C$), which characterizes promoter activity fluctuations, across gene expression levels in diverse genes and organisms. A biophysically plausible explanation for this invariance remains missing. Here, we show that this invariance imposes stringent constraints on minimal yet plausible models of transcriptional regulation, requiring at least four system states and non-equilibrium dynamics that break detailed balance. Using Bayesian inference on Drosophila gap gene expression data, we demonstrate that such models (i) accurately reproduce the observed $T_C$-invariance; (ii) remain robust to parameter perturbations; and (iii) maximize information transmission from transcription factor concentration to gene expression. These findings suggest that eukaryotic gene regulation has evolved to balance precision with reaction rate and energy dissipation constraints, favoring non-equilibrium architectures for optimal information transmission.

q-bio.MN↗

arXiv2023

Gene activity fully predicts transcriptional bursting dynamics

Transcription commonly occurs in bursts, with alternating productive (ON) and quiescent (OFF) periods, governing mRNA production rates. Yet, how transcription is regulated through bursting dynamics remains unresolved. Here, we conduct real-time measurements of endogenous transcriptional bursting with single-mRNA sensitivity. Leveraging the diverse transcriptional activities in early fly embryos, we uncover stringent relationships between bursting parameters. Specifically, we find that the durations of ON and OFF periods are linked. Regardless of the developmental stage or body-axis position, gene activity levels predict individual alleles' average ON and OFF periods. Lowly transcribing alleles predominantly modulate OFF periods (burst frequency), while highly transcribing alleles primarily tune ON periods (burst size). These relationships persist even under perturbations of cis-regulatory elements or trans-factors and account for bursting dynamics measured in other species. Our results suggest a novel mechanistic constraint governing bursting dynamics rather than a modular control of distinct parameters by distinct regulatory processes.

q-bio.MN↗

arXiv2021

Eukaryotic gene regulation at equilibrium, or non?

Models of transcriptional regulation that assume equilibrium binding of transcription factors have been very successful at predicting gene expression from sequence in bacteria. However, analogous equilibrium models do not perform as well in eukaryotes, most likely due to the largely out-of-equilibrium nature of eukaryotic regulatory processes. These processes come with unavoidable energy expenditure at the molecular level to support precise, reliable, or fast gene expression responses that could correspond to evolutionarily optimized regulatory strategies. Unfortunately, the space of possible non-equilibrium mechanisms is vast and predominantly uninteresting. The key question is therefore how this space can be navigated efficiently, to focus on mechanisms and models that are biologically relevant. In this review, we advocate for the normative role of theory - theory that prescribes rather than just describes - in providing such a focus. Theory should expand its remit beyond inferring models from data (by fitting), towards identifying non-equilibrium gene regulatory schemes (by optimizing) that may have been evolutionarily selected due to their favorable functional characteristics which outperform regulation at equilibrium. This approach can help us navigate the expanding complexity of regulatory architectures, and refocus the questions about the observed biological mechanisms from how they work towards why they have evolved in the first place. We illustrate our reasoning by toy examples for which we provide simulation code.

q-bio.MN↗

arXiv2017

Diverse spatial expression patterns emerge from common transcription bursting kinetics

In early development, regulation of transcription results in precisely positioned and highly reproducible expression patterns that specify cellular identities. How transcription, a fundamentally noisy molecular process, is regulated to achieve reliable embryonic patterning remains unclear. In particular, it is unknown how gene-specific regulation mechanisms affect kinetic rates of transcription, and whether there are common, global features that govern these rates across a genetic network. Here, we measure nascent transcriptional activity in the gap gene network of early Drosophila embryos and characterize the variability in absolute activity levels across expression boundaries. We demonstrate that boundary formation follows a common transcriptional principle: a single control parameter determines the distribution of transcriptional activity, regardless of gene identity, boundary position, or enhancer-promoter architecture. By employing a minimalist model of transcription, we infer kinetic rates of transcriptional bursting for these patterning genes; we find that the key regulatory parameter is the fraction of time a gene is in an actively transcribing state, while the rate of Pol II loading appears globally conserved. These results point to a universal simplicity underlying the apparently complex transcriptional processes responsible for early embryonic patterning and indicate a path to general rules in transcriptional regulation.

q-bio.SC↗