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Retinoic acid activates two pathways required for meiosis in mice.
Koubova, Jana; Hu, Yueh-Chiang; Bhattacharyya, Tanmoy; Soh, Y Q Shirleen; Gill, Mark E; Goodheart, Mary L; Hogarth, Cathryn A; Griswold, Michael D; Page, David C.
Affiliation
  • Koubova J; Whitehead Institute, Cambridge, Massachusetts, United States of America; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
  • Hu YC; Whitehead Institute, Cambridge, Massachusetts, United States of America.
  • Bhattacharyya T; Whitehead Institute, Cambridge, Massachusetts, United States of America.
  • Soh YQ; Whitehead Institute, Cambridge, Massachusetts, United States of America; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
  • Gill ME; Whitehead Institute, Cambridge, Massachusetts, United States of America.
  • Goodheart ML; Whitehead Institute, Cambridge, Massachusetts, United States of America; Howard Hughes Medical Institute, Whitehead Institute, Cambridge, Massachusetts, United States of America.
  • Hogarth CA; Center for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, Washington, United States of America.
  • Griswold MD; Center for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, Washington, United States of America.
  • Page DC; Whitehead Institute, Cambridge, Massachusetts, United States of America; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America; Howard Hughes Medical Institute, Whitehead Institute, Cambridge, Massachusetts, United States of America.
PLoS Genet ; 10(8): e1004541, 2014 Aug.
Article in En | MEDLINE | ID: mdl-25102060
ABSTRACT
In all sexually reproducing organisms, cells of the germ line must transition from mitosis to meiosis. In mice, retinoic acid (RA), the extrinsic signal for meiotic initiation, activates transcription of Stra8, which is required for meiotic DNA replication and the subsequent processes of meiotic prophase. Here we report that RA also activates transcription of Rec8, which encodes a component of the cohesin complex that accumulates during meiotic S phase, and which is essential for chromosome synapsis and segregation. This RA induction of Rec8 occurs in parallel with the induction of Stra8, and independently of Stra8 function, and it is conserved between the sexes. Further, RA induction of Rec8, like that of Stra8, requires the germ-cell-intrinsic competence factor Dazl. Our findings strengthen the importance of RA and Dazl in the meiotic transition, provide important details about the Stra8 pathway, and open avenues to investigate early meiosis through analysis of Rec8 induction and function.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Phosphoproteins / Tretinoin / Nuclear Proteins / RNA-Binding Proteins / Adaptor Proteins, Signal Transducing / Meiosis Limits: Animals Language: En Year: 2014 Type: Article

Full text: 1 Database: MEDLINE Main subject: Phosphoproteins / Tretinoin / Nuclear Proteins / RNA-Binding Proteins / Adaptor Proteins, Signal Transducing / Meiosis Limits: Animals Language: En Year: 2014 Type: Article