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Updated: Jun 13, 2026

Measuring the Kinetics of mRNA Transcription in Single Living Cells
Published on: August 25, 2011
A comparative analysis of promoter-proximal pausing reveals kinetic and distributional dimensions of variation
Xin Zeng1, Gilad Barshad2, Rebecca Hassett1
1Simons Center for Quantitative Biology, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Abstract:
Promoter-proximal pausing of RNA polymerase II is a key regulatory checkpoint in metazoan transcription. Despite extensive study of this process, quantitative methods for comparing pausing dynamics across biological contexts have been lacking. Here we introduce a model-based framework for rigorous comparative analysis of both pause-escape kinetics and pause-site distributions across genes, cell types, and species. An application to available PRO-seq datasets revealed striking differences across perturbations, and comparative analyses across cell types and species highlighted distinct patterns of variation in both pause-escape kinetics and pause-site distributions, with only weak coupling between them. Integration with chromatin and sequence features showed that lower pause-escape rates are associated with stronger promoter-proximal nucleosome occupancy, whereas changes in pause-site dispersion are associated with sequence features such as GC skew. Together, these results establish a quantitative framework for comparative analysis of promoter-proximal pausing and reveal kinetic and distributional dimensions of pausing variation across biological contexts.
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