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The core SWI/SNF catalytic subunit Brg1 regulates nephron progenitor cell proliferation and differentiation.
Basta, Jeannine M; Singh, Ajeet P; Robbins, Lynn; Stout, Lisa; Pherson, Michelle; Rauchman, Michael.
Affiliation
  • Basta JM; John T. Milliken Department of Medicine, Division of Nephrology, Washington University School of Medicine, St. Louis, Mo 63110 USA.
  • Singh AP; Division of Pediatric Hematology/Oncology, Departement of Pediatrics and Department of Biochemistry & Molecular Biology, Pennsylvania State University, Hershey, PA 17033 USA.
  • Robbins L; John T. Milliken Department of Medicine, Division of Nephrology, Washington University School of Medicine, St. Louis, Mo 63110 USA; VA St. Louis Health Care System, John Cochran Division, St. Louis, MO, 63106, USA.
  • Stout L; John T. Milliken Department of Medicine, Division of Nephrology, Washington University School of Medicine, St. Louis, Mo 63110 USA.
  • Pherson M; Department of Biochemistry & Molecular Biology, Saint Louis University, St. Louis, MO 63104 USA.
  • Rauchman M; John T. Milliken Department of Medicine, Division of Nephrology, Washington University School of Medicine, St. Louis, Mo 63110 USA; VA St. Louis Health Care System, John Cochran Division, St. Louis, MO, 63106, USA; Deaprtememt of Developmental Biology, Washington University School of Medicine, St. L
Dev Biol ; 464(2): 176-187, 2020 08 15.
Article in En | MEDLINE | ID: mdl-32504627
ABSTRACT
Chromatin-remodeling complexes play critical roles in establishing gene expression patterns in response to developmental signals. How these epigenetic regulators determine the fate of progenitor cells during development of specific organs is not well understood. We found that genetic deletion of Brg1 (Smarca4), the core enzymatic protein in SWI/SNF, in nephron progenitor cells leads to severe renal hypoplasia. Nephron progenitor cells were depleted in Six2-Cre, Brg1flx/flx mice due to reduced cell proliferation. This defect in self-renewal, together with impaired differentiation resulted in a profound nephron deficit in Brg1 mutant kidneys. Sall1, a transcription factor that is required for expansion and maintenance of nephron progenitors, associates with SWI/SNF. Brg1 and Sall1 bind promoters of many progenitor cell genes and regulate expression of key targets that promote their proliferation.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Transcription Factors / Nuclear Proteins / Cell Differentiation / DNA Helicases / Cell Proliferation / Nephrons Limits: Animals Language: En Journal: Dev Biol Year: 2020 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Transcription Factors / Nuclear Proteins / Cell Differentiation / DNA Helicases / Cell Proliferation / Nephrons Limits: Animals Language: En Journal: Dev Biol Year: 2020 Type: Article