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Updated: Jan 8, 2026

Single-Molecule Imaging of EWS-FLI1 Condensates Assembling on DNA
Published on: September 8, 2021
A model of transcriptional bursting dynamics based on coupling between chromatin and enhancer states
Ofri Axelrod1, Udi Binshtok1, Brian Gebelein2,3
1School of Neurobiology, Biochemistry, and Biophysics, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Abstract:
In recent years, it has become evident that transcription is not always a continuous process. Rather, many genes exhibit bursting behavior characterized by discrete periods of transcriptional activity and inactivity. While transcriptional bursting has been broadly observed across different organisms, from bacteria to mammals, we lack a mechanistic understanding of the molecular events that regulate this widespread process. Specifically, how the expression of a 'bursty' gene is quantitatively determined by different molecular factors such as the concentration of transcription factors (TF) and architecture of the enhancers is not well understood. Here, we introduce a model based on the interplay between chromatin state and TF binding in order to describe bursting dynamics. We leverage the widespread Monod-Wyman-Changeux two-state model to predict the dependence of transcriptional bursting dynamics on TF concentration, binding affinity, and number of TF binding sites. We use the model to qualitatively reproduce the behavior of bursting dynamics observed in the C. elegans gonad. Overall, we provide a tractable model for transcriptional bursting that offers mechanistic insights into the factors regulating transcriptional bursting and generates experimentally testable predictions capable of uncovering the molecular basis of this widespread process.
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