Retinoic acid activates two pathways required for meiosis in mice

PLoS Genet. 2014 Aug 7;10(8):e1004541. doi: 10.1371/journal.pgen.1004541. eCollection 2014 Aug.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / biosynthesis*
  • Adaptor Proteins, Signal Transducing / genetics
  • Animals
  • DNA Replication / genetics
  • Female
  • Gene Expression Regulation, Developmental / drug effects
  • Germ Cells / growth & development
  • Male
  • Meiosis / genetics*
  • Mice
  • Mitosis / genetics
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics*
  • Ovary / drug effects
  • Ovary / growth & development
  • Phosphoproteins / biosynthesis
  • Phosphoproteins / genetics*
  • RNA-Binding Proteins / biosynthesis
  • RNA-Binding Proteins / genetics*
  • Signal Transduction / drug effects
  • Testis / drug effects
  • Testis / growth & development
  • Transcription, Genetic / drug effects
  • Tretinoin / administration & dosage
  • Tretinoin / metabolism*

Substances

  • Adaptor Proteins, Signal Transducing
  • DAZL protein, mouse
  • Nuclear Proteins
  • Phosphoproteins
  • RNA-Binding Proteins
  • Rec8 protein, mouse
  • Stra8 protein, mouse
  • Tretinoin