Frequency modulation of transcriptional bursting enables sensitive and rapid gene regulation

Gene regulation is a complex non-equilibrium process. Here, we show that quantitating the temporal regulation of key gene states (transcriptionally inactive, active, and refractory) provides a parsimonious framework for analyzing gene regulation. Our theory makes two non-intuitive predictions. First...

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Bibliographic Details
Main Authors: Li, Congxin (Author) , Oehler, Michael (Author) , Brunner, Michael (Author) , Höfer, Thomas (Author)
Format: Article (Journal)
Language:English
Published: 14 February 2018
In: Cell systems
Year: 2018, Volume: 6, Issue: 4, Pages: 409-423.e11
ISSN:2405-4720
DOI:10.1016/j.cels.2018.01.012
Online Access:Verlag, Volltext: https://doi.org/10.1016/j.cels.2018.01.012
Verlag: http://www.sciencedirect.com/science/article/pii/S2405471218300127
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Author Notes:Congxin Li, François Cesbron, Michael Oehler, Michael Brunner, Thomas Höfer
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Summary:Gene regulation is a complex non-equilibrium process. Here, we show that quantitating the temporal regulation of key gene states (transcriptionally inactive, active, and refractory) provides a parsimonious framework for analyzing gene regulation. Our theory makes two non-intuitive predictions. First, for transcription factors (TFs) that regulate transcription burst frequency, as opposed to amplitude or duration, weak TF binding is sufficient to elicit strong transcriptional responses. Second, refractoriness of a gene after a transcription burst enables rapid responses to stimuli. We validate both predictions experimentally by exploiting the natural, optogenetic-like responsiveness of the Neurospora GATA-type TF White Collar Complex (WCC) to blue light. Further, we demonstrate that differential regulation of WCC target genes is caused by different gene activation rates, not different TF occupancy, and that these rates are tuned by both the core promoter and the distance between TF-binding site and core promoter. In total, our work demonstrates the relevance of a kinetic, non-equilibrium framework for understanding transcriptional regulation.
Item Description:Gesehen am 27.02.2020
Physical Description:Online Resource
ISSN:2405-4720
DOI:10.1016/j.cels.2018.01.012