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EED, a member of the polycomb group, is required for nephron differentiation and the maintenance of nephron progenitor cells.
Zhang, Le; Ettou, Sandrine; Khalid, Myda; Taglienti, Mary; Jain, Dhawal; Jung, Youngsook L; Seager, Catherine; Liu, Yongqing; Ng, Kar-Hui; Park, Peter J; Kreidberg, Jordan A.
Affiliation
  • Zhang L; Department of Urology, Boston Children's Hospital, Boston, MA 02115, USA.
  • Ettou S; Division of Nephrology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
  • Khalid M; Department of Urology, Boston Children's Hospital, Boston, MA 02115, USA.
  • Taglienti M; Department of Surgery, Harvard Medical School, Boston, MA 02115, USA.
  • Jain D; Division of Nephrology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
  • Jung YL; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA.
  • Seager C; Department of Urology, Boston Children's Hospital, Boston, MA 02115, USA.
  • Liu Y; Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.
  • Ng KH; Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.
  • Park PJ; Department of Urology, Boston Children's Hospital, Boston, MA 02115, USA.
  • Kreidberg JA; Department of Surgery, Harvard Medical School, Boston, MA 02115, USA.
Development ; 145(14)2018 07 18.
Article in En | MEDLINE | ID: mdl-29945864
ABSTRACT
Epigenetic regulation of gene expression has a crucial role allowing for the self-renewal and differentiation of stem and progenitor populations during organogenesis. The mammalian kidney maintains a population of self-renewing stem cells that differentiate to give rise to thousands of nephrons, which are the functional units that carry out filtration to maintain physiological homeostasis. The polycomb repressive complex 2 (PRC2) epigenetically represses gene expression during development by placing the H3K27me3 mark on histone H3 at promoter and enhancer sites, resulting in gene silencing. To understand the role of PRC2 in nephron differentiation, we conditionally inactivated the Eed gene, which encodes a nonredundant component of the PRC2 complex, in nephron progenitor cells. Resultant kidneys were smaller and showed premature loss of progenitor cells. The progenitors in Eed mutant mice that were induced to differentiate did not develop into properly formed nephrons. Lhx1, normally expressed in the renal vesicle, was overexpressed in kidneys of Eed mutant mice. Thus, PRC2 has a crucial role in suppressing the expression of genes that maintain the progenitor state, allowing nephron differentiation to proceed.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Differentiation / Gene Expression Regulation, Developmental / Epigenesis, Genetic / Polycomb Repressive Complex 2 / Nephrons Limits: Animals Language: En Journal: Development Journal subject: BIOLOGIA / EMBRIOLOGIA Year: 2018 Document type: Article Affiliation country: United States Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Differentiation / Gene Expression Regulation, Developmental / Epigenesis, Genetic / Polycomb Repressive Complex 2 / Nephrons Limits: Animals Language: En Journal: Development Journal subject: BIOLOGIA / EMBRIOLOGIA Year: 2018 Document type: Article Affiliation country: United States Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM