Stage- and subunit-specific functions of polycomb repressive complex 2 in bladder urothelial formation and regeneration

Author:

Guo Chunming1,Balsara Zarine R.1,Hill Warren G.2ORCID,Li Xue1ORCID

Affiliation:

1. Department of Urology and Department of Surgery, Boston Children's Hospital, Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USA

2. Laboratory of Voiding Dysfunction, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115, USA

Abstract

Urothelium is the protective lining of the urinary tract. The mechanisms underlying urothelial formation and maintenance are largely unknown. Here, we report the stage-specific roles of PRC2 epigenetic regulators in embryonic and adult urothelial progenitors. Without Eed, the obligatory subunit of PRC2, embryonic urothelial progenitors demonstrate reduced proliferation with concomitant dysregulation of genes including Cdkn2a(p16), Cdkn2b(p15) and Shh. These mutants display premature differentiation of Keratin 5-positive (Krt5+) basal cells and ectopic expression of squamous-like differentiation markers. Deletion of Ezh2, the major enzymatic component of PRC2, causes upregulation of Upk3a+ superficial cells. Unexpectedly, Eed and Eed/Ezh2 double mutants exhibit delayed superficial cell differentiation. Furthermore, Eed regulates proliferative and regenerative capacity of adult urothelial progenitors and prevents precocious differentiation Collectively, these findings uncover the epigenetic mechanism by which PRC2 controls urothelial progenitor cell fate and timing of differentiation, and further suggest an epigenetic basis of urothelial maintenance and regeneration.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Division of Cancer Prevention, National Cancer Institute

American Heart Association

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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