Transcriptional and epigenomic profiling identifies YAP signaling as a key regulator of intestinal epithelium maturation

Author:

Pikkupeura Laura M.12ORCID,Bressan Raul B.13,Guiu Jordi14ORCID,Chen Yun12,Maimets Martti13ORCID,Mayer Daniela13ORCID,Schweiger Pawel J.13,Hansen Stine L.13ORCID,Maciag Grzegorz J.13ORCID,Larsen Hjalte L.13ORCID,Lõhmussaar Kadi3,Pedersen Marianne Terndrup1,Teves Joji M. Yap13,Bornholdt Jette12,Benes Vladimir5ORCID,Sandelin Albin12ORCID,Jensen Kim B.13ORCID

Affiliation:

1. BRIC - Biotech Research and Innovation Centre, University of Copenhagen, Copenhagen N DK-2200, Denmark.

2. Bioinformatics Center, Department of Biology, University of Copenhagen, Copenhagen N DK-2200, Denmark.

3. Novo Nordisk Foundation Center for Stem Cell Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen N DK-2200, Denmark.

4. Institut d’Investigació Biomèdica de Bellvitge–IDIBELL, L’Hospitalet de Llobregat, 3a planta, Av. Granvia de l’Hospitalet 199, Hospitalet de Llobregat 08908, Spain.

5. GeneCore, EMBL, Heidelberg, Germany.

Abstract

During intestinal organogenesis, equipotent epithelial progenitors mature into phenotypically distinct stem cells that are responsible for lifelong maintenance of the tissue. While the morphological changes associated with the transition are well characterized, the molecular mechanisms underpinning the maturation process are not fully understood. Here, we leverage intestinal organoid cultures to profile transcriptional, chromatin accessibility, DNA methylation, and three-dimensional (3D) chromatin conformation landscapes in fetal and adult epithelial cells. We observed prominent differences in gene expression and enhancer activity, which are accompanied by local changes in 3D organization, DNA accessibility, and methylation between the two cellular states. Using integrative analyses, we identified sustained Yes-Associated Protein (YAP) transcriptional activity as a major gatekeeper of the immature fetal state. We found the YAP-associated transcriptional network to be regulated at various levels of chromatin organization and likely to be coordinated by changes in extracellular matrix composition. Together, our work highlights the value of unbiased profiling of regulatory landscapes for the identification of key mechanisms underlying tissue maturation.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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