bioRxiv (Cold Spring Harbor Laboratory) · 2021 · 28 citations · 40 references
Life SciencesCell BiologyMolecular BiologyGene ExpressionTranscriptionTranscriptional RegulationIntermolecular InteractionsMacromolecular AssemblyMultivalent InteractionsPhase SeparationProtein Complex AssemblyProtein-nucleic Acid InteractionsChromatin Phase SeparationGene Activation MechanismsPhase Separation In Chromatin OrganizationTranscription Factor ComplexesTranscription Factor OligomerizationTranscriptional Activation
Summary Transcription factors (TFs) consist of a DNA binding and an activation domain (AD) that are considered to be independent and exchangeable modules. However, recent studies conclude that also the physico-chemical properties of the AD can control TF assembly at chromatin by driving a phase separation into transcriptional condensates. Here, we dissected transcription activation by comparing different synthetic TFs at a reporter gene array with real-time single-cell fluorescence microscopy readouts. In these experiments, binding site occupancy, residence time and co-activator recruitment in relation to multivalent TF interactions were compared. While phase separation propensity and activation strength of the AD were correlated, the actual formation of liquid-like TF droplets had a neutral or inhibitory effect on transcription activation. Rather, we conclude that multivalent AD mediated interactions increase the transcription activation capacity of a TF by stabilizing chromatin binding and mediating the recruitment of co-activators independent of phase separation.
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