The transcription factor grainyhead-like 2 regulates the molecular composition of the epithelial apical junctional complex

Author:

Werth Max12,Walentin Katharina12,Aue Annekatrin12,Schönheit Jörg1,Wuebken Anne1,Pode-Shakked Naomi3,Vilianovitch Larissa1,Erdmann Bettina1,Dekel Benjamin3,Bader Michael1,Barasch Jonathan4,Rosenbauer Frank1,Luft Friedrich C.12,Schmidt-Ott Kai M.12

Affiliation:

1. Max-Delbrück Center for Molecular Medicine, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.

2. Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin, Campus Buch, 13125 Berlin, Germany.

3. Department of Pediatrics and Pediatric Stem Cell Research Institute, Sheba Medical Center, Tel Hashomer, 52621, Israel.

4. Department of Medicine, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.

Abstract

Differentiation of epithelial cells and morphogenesis of epithelial tubes or layers is closely linked with the establishment and remodeling of the apical junctional complex, which includes adherens junctions and tight junctions. Little is known about the transcriptional control of apical junctional complex components. Here, we show that the transcription factor grainyhead-like 2 (Grhl2), an epithelium-specific mammalian homolog of Drosophila Grainyhead, is essential for adequate expression of the adherens junction gene E-cadherin and the tight junction gene claudin 4 (Cldn4) in several types of epithelia, including gut endoderm, surface ectoderm and otic epithelium. We have generated Grhl2 mutant mice to demonstrate defective molecular composition of the apical junctional complex in these compartments that coincides with the occurrence of anterior and posterior neural tube defects. Mechanistically, we show that Grhl2 specifically associates with cis-regulatory elements localized at the Cldn4 core promoter and within intron 2 of the E-cadherin gene. Cldn4 promoter activity in epithelial cells is crucially dependent on the availability of Grhl2 and on the integrity of the Grhl2-associated cis-regulatory element. At the E-cadherin locus, the intronic Grhl2-associated cis-regulatory region contacts the promoter via chromatin looping, while loss of Grhl2 leads to a specific decrease of activating histone marks at the E-cadherin promoter. Together, our data provide evidence that Grhl2 acts as a target gene-associated transcriptional activator of apical junctional complex components and, thereby, crucially participates in epithelial differentiation.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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