Enhancer binding kinetics explain transcription factor hub formation

Transcription factors (TFs) form dynamic, high-concentration clusters, condensates, or hubs, proposed to increase TF binding frequency at target enhancers. However, how enhancer sequence shapes hub properties remains unclear. We developed a live imaging–based framework to quantify the spatiotemporal relationship between TF hubs and actively transcribed genes in live Drosophila embryos. Examining hubs formed by the TF Dorsal across enhancers with defined binding site composition, we find that hub enrichment and persistence scale with the number of Dorsal binding motifs. However, these hub properties do not predict transcriptional bursts for a given enhancer. Combining quantitative imaging with computational modeling, we show that Dorsal hub formation can be explained by TF-DNA binding kinetics alone. These findings support a model in which TF hubs emerge from enhancer-encoded TF-DNA interactions rather than higher-order regulatory assemblies.

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Publication Details

Journal
Science Advances
Published
2026-10-09
DOI
https://doi.org/10.1126/sciadv.aeh1086
Primary Topic
Genomics and Chromatin Dynamics
Type
article
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article

Enhancer binding kinetics explain transcription factor hub formation

Samantha Fallacaro, Apratim Mukherjee, Manya Kapoor, Meghan A. Turner et al.
Science Advances
Genomics and Chromatin Dynamics
article

Enhancer binding kinetics explain transcription factor hub formation

Samantha Fallacaro, Apratim Mukherjee, Manya Kapoor, Meghan A. Turner, Mustafa Mir, Hernán G. García, Lillian Encarnation
article en

Abstract

Transcription factors (TFs) form dynamic, high-concentration clusters, condensates, or hubs, proposed to increase TF binding frequency at target enhancers. However, how enhancer sequence shapes hub properties remains unclear. We developed a live imaging–based framework to quantify the spatiotemporal relationship between TF hubs and actively transcribed genes in live Drosophila embryos. Examining hubs formed by the TF Dorsal across enhancers with defined binding site composition, we find that hub enrichment and persistence scale with the number of Dorsal binding motifs. However, these hub properties do not predict transcriptional bursts for a given enhancer. Combining quantitative imaging with computational modeling, we show that Dorsal hub formation can be explained by TF-DNA binding kinetics alone. These findings support a model in which TF hubs emerge from enhancer-encoded TF-DNA interactions rather than higher-order regulatory assemblies.

Science AdvancesVol. 12(41)
QB3 (US), Children's Hospital of Philadelphia (US), Howard Hughes Medical Institute (US), Chan Zuckerberg Biohub San Francisco (US), University of Pennsylvania (US), University of California, Berkeley (US)
Openalex Percentile: Top 23%
Genomics and Chromatin Dynamics
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Enhancer binding kinetics explain transcription factor hub formation — Samantha Fallacaro, Apratim Mukherjee, et al. · Science Advances (2026) | TGRS Research Map | TGRS