Bicoid-nucleosome competition sets a concentration threshold for transcription constrained by genome replication

Transcription factors (TFs) regulate gene expression despite constraints from chromatin structure and the cell cycle. Here, we examine the concentration-dependent regulation of hunchback by the Bicoid morphogen through a combination of quantitative imaging, mathematical modeling, and epigenomics in Drosophila embryos. By live imaging of MS2 reporters, we find that, following mitosis, the timing of transcriptional activation driven by the hunchback P2 (hbP2) enhancer directly reflects Bicoid concentration. We build a stochastic model that can explain in vivo onset time distributions by accounting for both the competition between Bicoid and nucleosomes at hbP2 and a negative influence of DNA replication on transcriptional elongation. Experimental modulation of nucleosome stability alters onset time distributions and the posterior boundary of hunchback expression. We conclude that TF-nucleosome competition is the molecular mechanism whereby the Bicoid morphogen gradient specifies the posterior boundary of hunchback expression.

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Publication Details

Journal
Cell Reports
Published
2025-08-01
DOI
https://doi.org/10.1016/j.celrep.2025.116121
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Bicoid-nucleosome competition sets a concentration threshold for transcription constrained by genome replication

Shelby A. Blythe, Niall M. Mangan, Eleanor A Degen, Corinne Croslyn
Cell Reports
Genomics and Chromatin Dynamics
article

Bicoid-nucleosome competition sets a concentration threshold for transcription constrained by genome replication

Shelby A. Blythe, Niall M. Mangan, Eleanor A Degen, Corinne Croslyn
article en

Abstract

Transcription factors (TFs) regulate gene expression despite constraints from chromatin structure and the cell cycle. Here, we examine the concentration-dependent regulation of hunchback by the Bicoid morphogen through a combination of quantitative imaging, mathematical modeling, and epigenomics in Drosophila embryos. By live imaging of MS2 reporters, we find that, following mitosis, the timing of transcriptional activation driven by the hunchback P2 (hbP2) enhancer directly reflects Bicoid concentration. We build a stochastic model that can explain in vivo onset time distributions by accounting for both the competition between Bicoid and nucleosomes at hbP2 and a negative influence of DNA replication on transcriptional elongation. Experimental modulation of nucleosome stability alters onset time distributions and the posterior boundary of hunchback expression. We conclude that TF-nucleosome competition is the molecular mechanism whereby the Bicoid morphogen gradient specifies the posterior boundary of hunchback expression.

Cell ReportsVol. 44(8)
Northwestern University (US)
National Science Foundation, Pew Charitable Trusts, Simons Foundation, National Institute of General Medical Sciences, National Institute of Child Health and Human Development
Zero hunger
Openalex Percentile: Top 82%
Genomics and Chromatin Dynamics
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