Single-molecule imaging reveals the interplay between transcription factors, nucleosomes, and transcriptional bursting

• DOI: 10.1101/404681
• Publication Date: 2018-08-31T13:55:31Z
• Authors: Benjamin T. Donovan; Anh Huynh; David A. Ball; Michael G. Poirier; Daniel R. Larson; Matthew L. Ferguson; Tineke L. Lenstra
• Keywords: transcriptional activators; 0301 basic medicine; binding dynamics; 570; 03 medical and health sciences; Physics; burst size; chromatin; 610; stochastic; BRC

SummaryTranscription factors show rapid and reversible binding to chromatin in living cells, and transcription occurs in sporadic bursts, but how these phenomena are related is unknown. Using a combination of in vitro and in vivo single-molecule imaging approaches, we directly correlated binding of the transcription factor Gal4 with the transcriptional bursting kinetics of the Gal4 target genes GAL3 and GAL10 in living yeast cells. We find that Gal4 dwell times sets the transcriptional burst size. Gal4 dwell time depends on the affinity of the binding site and is reduced by orders of magnitude by nucleosomes. Using a novel imaging platform, we simultaneously tracked transcription factor binding and transcription at one locus, revealing the timing and correlation between Gal4 binding and transcription. Collectively, our data support a model where multiple polymerases initiate during a burst as long as the transcription factor is bound to DNA, and a burst terminates upon transcription factor dissociation.