Post-transcriptional control of gene expression during mouse oogenesis

Results Probl Cell Differ. 2012;55:1-21. doi: 10.1007/978-3-642-30406-4_1.


Post-transcriptional mechanisms play a central role in regulating gene expression during oogenesis and early embryogenesis. Growing oocytes accumulate an enormous quantity of messenger RNAs (mRNAs), but transcription decreases dramatically near the end of growth and is undetectable during meiotic maturation. Following fertilization, the embryo is initially transcriptionally inactive and then becomes active at a species-specific stage of early cleavage. Meanwhile, beginning during maturation and continuing after fertilization, the oocyte mRNAs are eliminated, allowing the embryonic genome to assume control of development. How the mammalian oocyte manages the storage, translation, and degradation of the huge quantity and diversity of mRNAs that it harbours has been the focus of enormous research effort and is the subject of this review. We discuss the roles of sequences within the 3'-untranslated region of certain mRNAs and the proteins that bind to them, sequence-non-specific RNA-binding proteins, and recent studies implicating ribonucleoprotein processing (P-) bodies and cytoplasmic lattices. We also discuss mechanisms that may control the temporally regulated translational activation of different mRNAs during meiotic maturation, as well as the signals that trigger silencing and degradation of the oocyte mRNAs. We close by highlighting areas for future research including the potential key role of small RNAs in regulating gene expression in oocytes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cytoplasmic Granules / metabolism
  • Embryo, Mammalian / metabolism
  • Female
  • Fertilization / physiology
  • Gene Expression Regulation / physiology*
  • Meiosis / physiology
  • Mice
  • Oocytes / cytology
  • Oocytes / metabolism*
  • Oogenesis / physiology*
  • Protein Biosynthesis / physiology
  • RNA, Messenger / metabolism
  • Ribonucleoproteins / metabolism


  • RNA, Messenger
  • Ribonucleoproteins