Transcriptional regulation of the thymus master regulator Foxn1

Author:

Kadouri Noam1ORCID,Givony Tal1ORCID,Nevo Shir1ORCID,Hey Joschka23ORCID,Ben Dor Shifra4ORCID,Damari Golda5,Dassa Bareket4ORCID,Dobes Jan1ORCID,Weichenhan Dieter2,Bähr Marion2,Paulsen Michelle67ORCID,Haffner-Krausz Rebecca5ORCID,Mall Marcus A.678ORCID,Plass Christoph2ORCID,Goldfarb Yael1ORCID,Abramson Jakub1ORCID

Affiliation:

1. Department of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot, Israel.

2. Division of Cancer Epigenomics, German Cancer Research Center (DKFZ), Heidelberg, Germany.

3. Ruprecht Karl University of Heidelberg, Heidelberg, Germany.

4. Bioinformatics Unit, Weizmann Institute of Science, Rehovot, Israel.

5. Department of Veterinary Resources, Weizmann Institute of Science, Rehovot, Israel.

6. Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.

7. Department of Translational Pulmonology, University of Heidelberg, Heidelberg, Germany.

8. Charité-Universitätsmedizin Berlin, Berlin, Germany.

Abstract

FOXN1 is a transcription factor critical for the development of both thymic epithelial cell (TEC) and hair follicle cell (HFC) compartments. However, mechanisms controlling its expression remain poorly understood. To address this question, we performed thorough analyses of the evolutionary conservation and chromatin status of the Foxn1 locus in different tissues and states and identified several putative cis-regulatory regions unique to TECs versus HFCs. Furthermore, experiments using genetically modified mice with specific deletions in the Foxn1 locus and additional bioinformatic analyses helped us identify key regions and transcription factors involved in either positive or negative regulation of Foxn1 in both TECs and HFCs. Specifically, we identified SIX1 and FOXN1 itself as key factors inducing Foxn1 expression in embryonic and neonatal TECs. Together, our data provide important mechanistic insights into the transcriptional regulation of the Foxn1 gene in TEC versus HFC and highlight the role of FOXN1 in its autoregulation.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine,Immunology

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