Maternal mRNAs with distinct 3′ UTRs define the temporal pattern of Ccnb1 synthesis during mouse oocyte meiotic maturation

  1. Marco Conti2,3,4
  1. 1State Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University (CAU), Beijing 100193, People's Republic of China;
  2. 2Center for Reproductive Sciences, University of California at San Francisco, San Francisco California 94143, USA;
  3. 3Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California at San Francisco, San Francisco, California 94143, USA;
  4. 4Department of Obstetrics and Gynecology and Reproductive Sciences, University of California at San Francisco, San Francisco, California 94143, USA;
  5. 5Department of Biological Sciences, Inje University, Gimhae 621-749, Republic of Korea
  1. Corresponding author: contim{at}obgyn.ucsf.edu

Abstract

The final stages of female gamete maturation occur in the virtual absence of transcription, with gene expression driven by a program of selective unmasking, translation, and degradation of maternal mRNAs. Here we demonstrate that the timing of Ccnb1 mRNA translation in mouse oocytes is dependent on the presence of transcripts with different 3′ untranslated regions (UTRs). This 3′ UTR heterogeneity directs distinct temporal patterns of translational activation or repression. Inclusion or exclusion of cis-acting elements is responsible for these divergent regulations. Our findings reveal an additional layer of translation control through alternative polyadenylation usage required to fine-tune the timing of meiosis progression.

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Footnotes

  • Received February 17, 2017.
  • Accepted July 14, 2017.

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