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TAF4b Regulates Oocyte-Specific Genes Essential for Meiosis.
Grive, Kathryn J; Gustafson, Eric A; Seymour, Kimberly A; Baddoo, Melody; Schorl, Christoph; Golnoski, Kayla; Rajkovic, Aleksandar; Brodsky, Alexander S; Freiman, Richard N.
Affiliation
  • Grive KJ; MCB Graduate Program, Brown University, Providence, Rhode Island, United States of America.
  • Gustafson EA; MCB Department, Brown University, Providence, Rhode Island, United States of America.
  • Seymour KA; MCB Department, Brown University, Providence, Rhode Island, United States of America.
  • Baddoo M; School of Medicine, Tulane University, New Orleans, Louisiana, United States of America.
  • Schorl C; MCB Department, Brown University, Providence, Rhode Island, United States of America.
  • Golnoski K; Magee Women's Research Institute, Pittsburgh, Pennsylvania, United States of America.
  • Rajkovic A; Magee Women's Research Institute, Pittsburgh, Pennsylvania, United States of America.
  • Brodsky AS; Department of Pathology, Rhode Island Hospital and Brown University, Providence, Rhode Island, United States of America.
  • Freiman RN; MCB Department, Brown University, Providence, Rhode Island, United States of America.
PLoS Genet ; 12(6): e1006128, 2016 06.
Article in En | MEDLINE | ID: mdl-27341508
TAF4b is a gonadal-enriched subunit of the general transcription factor TFIID that is implicated in promoting healthy ovarian aging and female fertility in mice and humans. To further explore the potential mechanism of TAF4b in promoting ovarian follicle development, we analyzed global gene expression at multiple time points in the human fetal ovary. This computational analysis revealed coordinate expression of human TAF4B and critical regulators and effectors of meiosis I including SYCP3, YBX2, STAG3, and DAZL. To address the functional relevance of this analysis, we turned to the embryonic Taf4b-deficient mouse ovary where, for the first time, we demonstrate, severe deficits in prophase I progression as well as asynapsis in Taf4b-deficient oocytes. Accordingly, TAF4b occupies the proximal promoters of many essential meiosis and oogenesis regulators, including Stra8, Dazl, Figla, and Nobox, and is required for their proper expression. These data reveal a novel TAF4b function in regulating a meiotic gene expression program in early mouse oogenesis, and support the existence of a highly conserved TAF4b-dependent gene regulatory network promoting early oocyte development in both mice and women.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oocytes / TATA-Binding Protein Associated Factors / Transcription Factor TFIID / Meiosis Limits: Animals / Female / Humans / Male Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2016 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oocytes / TATA-Binding Protein Associated Factors / Transcription Factor TFIID / Meiosis Limits: Animals / Female / Humans / Male Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2016 Type: Article Affiliation country: United States