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Dynamic Epistasis Analysis Reveals How Chromatin Remodeling Regulates Transcriptional Bursting

bioRxiv (Cold Spring Harbor Laboratory)(2021)

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摘要
Transcriptional bursting has been linked to the stochastic positioning of nucleosomes. However, how bursting is regulated by the remodeling of promoter nucleosomes is unknown. Here, we use single-molecule live-cell imaging of GAL10 transcription in Saccharomyces cerevisiae to measure how bursting changes upon combined perturbations of chromatin remodelers, the transcription factor Gal4 and preinitiation complex components. Using dynamic epistasis analysis, we reveal how the remodeling of different nucleosomes regulates transcriptional bursting parameters. At the nucleosome covering the Gal4 binding sites, RSC and Gal4 binding synergistically facilitate each burst. Conversely, nucleosome remodeling at the TATA box controls only the first burst upon galactose induction. At canonical TATA boxes, the nucleosomes are displaced by TBP binding to allow for transcription activation even in the absence of remodelers. Overall, our results reveal how promoter nucleosome remodeling together with Gal4 and preinitiation complex binding regulates transcriptional bursting. Using single-molecule transcription imaging upon perturbations to nucleosome remodelers, the transcription factor and the transcriptional machinery, Brouwer et al. reveal how remodeling of promoter nucleosomes regulates the kinetics of transcription.
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关键词
Nucleosome Positioning,Transcriptomics
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