Masking, unmasking, and regulated polyadenylation cooperate in the translational control of a dormant mRNA in mouse oocytes

Genes Dev. 1998 Aug 15;12(16):2535-48. doi: 10.1101/gad.12.16.2535.

Abstract

The mechanisms responsible for translational silencing of certain mRNAs in growing oocytes, and for their awakening during meiotic maturation, are not completely elucidated. We show that binding of a approximately 80-kD protein to a UA-rich element in the 3' UTR of tissue-type plasminogen activator mRNA, a mouse oocyte mRNA that is translated during meiotic maturation, silences the mRNA in primary oocytes. Translation can be triggered by injecting a competitor transcript that displaces this silencing factor, without elongation of a pre-existing short poly(A) tail, the presence of which is mandatory. During meiotic maturation, cytoplasmic polyadenylation is necessary to maintain a poly(A) tail, but the determining event for translational activation appears to be the modification or displacement of the silencing factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding, Competitive
  • Cells, Cultured
  • Cytoplasm / metabolism
  • Meiosis / genetics
  • Mice
  • Oocytes / physiology*
  • Oogenesis / genetics
  • Protein Biosynthesis*
  • RNA, Messenger / physiology*
  • Tissue Plasminogen Activator / genetics
  • Tissue Plasminogen Activator / metabolism

Substances

  • RNA, Messenger
  • Tissue Plasminogen Activator