GRHL and PGR control WNT4 expression via 3D looping of conserved and species-specific enhancers

Developmental gene expression is tightly regulated by tissue-specific enhancers. Understanding this process in the context of the three-dimensional (3D) genome requires dedicated interrogation on a per gene and per tissue basis. Here, we functionally dissect the mechanisms that regulate Wnt4/WNT4 gene expression. We focus our efforts on the mouse mammary gland and human breast, where Wnt4/WNT4 expression is restricted to hormone-responsive luminal epithelial cells and generally assumed to lie downstream of progesterone. Using freshly isolated cells and cell lines, we map the Wnt4/WNT4 enhancer network, reveal Grainyhead-like (GRHL) proteins as novel co-regulators of Wnt4/WNT4 expression, and identify a conserved distal enhancer that physically loops to Wnt4/WNT4. We integrate our findings to propose a working model in which a conserved distal chromatin hub, bound by CTCF and GRHL, recruits other species-specific enhancers, to facilitate PGR-dependent and -independent Wnt4/WNT4 gene regulation via 3D chromatin looping.

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Publication Details

Journal
Cell Reports
Published
2026-06-25
DOI
https://doi.org/10.1016/j.celrep.2026.117575
Primary Topic
Wnt/β-catenin signaling in development and cancer
Type
article
Field-Weighted Citation Impact
0.00

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article

GRHL and PGR control WNT4 expression via 3D looping of conserved and species-specific enhancers

Paul Krimpenfort, Katrin E. Wiese, Renée van Amerongen, Linda Henneman et al.
Cell Reports
Wnt/β-catenin signaling in development and cancer
article

GRHL and PGR control WNT4 expression via 3D looping of conserved and species-specific enhancers

Paul Krimpenfort, Katrin E. Wiese, Renée van Amerongen, Linda Henneman, Ingeborg B. Hooijkaas, Nika Heijmans, Marleen T. Aarts, Yorick B.C. van de Grift, Antonius L. van Boxtel, Colin E.J. Pritchard
article en

Abstract

Developmental gene expression is tightly regulated by tissue-specific enhancers. Understanding this process in the context of the three-dimensional (3D) genome requires dedicated interrogation on a per gene and per tissue basis. Here, we functionally dissect the mechanisms that regulate Wnt4/WNT4 gene expression. We focus our efforts on the mouse mammary gland and human breast, where Wnt4/WNT4 expression is restricted to hormone-responsive luminal epithelial cells and generally assumed to lie downstream of progesterone. Using freshly isolated cells and cell lines, we map the Wnt4/WNT4 enhancer network, reveal Grainyhead-like (GRHL) proteins as novel co-regulators of Wnt4/WNT4 expression, and identify a conserved distal enhancer that physically loops to Wnt4/WNT4. We integrate our findings to propose a working model in which a conserved distal chromatin hub, bound by CTCF and GRHL, recruits other species-specific enhancers, to facilitate PGR-dependent and -independent Wnt4/WNT4 gene regulation via 3D chromatin looping.

Cell ReportsVol. 45(7)
Oncode Institute (NL), Amsterdam University of Applied Sciences (NL)
Nederlandse Organisatie voor Wetenschappelijk Onderzoek, HORIZON EUROPE Marie Sklodowska-Curie Actions
Zero hunger
Openalex Percentile: Top 11%
Wnt/β-catenin signaling in development and cancer
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