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SWI/SNF chromatin remodeling subunit Smarca4/BRG1 is essential for female fertility†.
Abedini, Atefeh; Landry, David A; Macaulay, Angus D; Vaishnav, Het; Parbhakar, Ashna; Ibrahim, Dalia; Salehi, Reza; Maranda, Vincent; Macdonald, Elizabeth; Vanderhyden, Barbara C.
Afiliación
  • Abedini A; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
  • Landry DA; Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Macaulay AD; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
  • Vaishnav H; Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Parbhakar A; Interdisciplinary School of Health Sciences, University of Ottawa, Ottawa, ON, Canada.
  • Ibrahim D; Chronic Diseases Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Salehi R; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
  • Maranda V; Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Macdonald E; Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Vanderhyden BC; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
Biol Reprod ; 108(2): 279-291, 2023 02 13.
Article en En | MEDLINE | ID: mdl-36440965
ABSTRACT
Mammalian folliculogenesis is a complex process that involves the regulation of chromatin structure for gene expression and oocyte meiotic resumption. The SWI/SNF complex is a chromatin remodeler using either Brahma-regulated gene 1 (BRG1) or BRM (encoded by Smarca4 and Smarca2, respectively) as its catalytic subunit. SMARCA4 loss of expression is associated with a rare type of ovarian cancer; however, its function during folliculogenesis remains poorly understood. In this study, we describe the phenotype of BRG1 mutant mice to better understand its role in female fertility. Although no tumor emerged from BRG1 mutant mice, conditional depletion of Brg1 in the granulosa cells (GCs) of Brg1fl/fl;Amhr2-Cre mice caused sterility, whereas conditional depletion of Brg1 in the oocytes of Brg1fl/fl;Gdf9-Cre mice resulted in subfertility. Recovery of cumulus-oocyte complexes after natural mating or superovulation showed no significant difference in the Brg1fl/fl;Amhr2-Cre mutant mice and significantly fewer oocytes in the Brg1fl/fl;Gdf9-Cre mutant mice compared with controls, which may account for the subfertility. Interestingly, the evaluation of oocyte developmental competence by in vitro culture of retrieved two-cell embryos indicated that oocytes originating from the Brg1fl/fl;Amhr2-Cre mice did not reach the blastocyst stage and had higher rates of mitotic defects, including micronuclei. Together, these results indicate that BRG1 plays an important role in female fertility by regulating granulosa and oocyte functions during follicle growth and is needed for the acquisition of oocyte developmental competence.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromatina / Neoplasias Límite: Animals Idioma: En Revista: Biol Reprod Año: 2023 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromatina / Neoplasias Límite: Animals Idioma: En Revista: Biol Reprod Año: 2023 Tipo del documento: Article País de afiliación: Canadá