Genome-wide analysis reveals a switch in the translational program upon oocyte meiotic resumption. Issue 6 (23rd January 2020)

• Record Type: Journal Article
• Authors: Luong, Xuan G; Daldello, Enrico Maria; Rajkovic, Gabriel; Yang, Cai-Rong; Conti, Marco
• Is Part Of: Nucleic acids research. Volume 48:Issue 6(2020)
• Page Start: 3257
• Page End: 3276
• Publication Date: 2020-01-23
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gkaa010
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: During oocyte maturation, changes in gene expression depend exclusively on translation and degradation of maternal mRNAs rather than transcription. Execution of this translation program is essential for assembling the molecular machinery required for meiotic progression, fertilization, and embryo development. With the present study, we used a RiboTag/RNA-Seq approach to explore the timing of maternal mRNA translation in quiescent oocytes as well as in oocytes progressing through the first meiotic division. This genome-wide analysis reveals a global switch in maternal mRNA translation coinciding with oocyte re-entry into the meiotic cell cycle. Messenger RNAs whose translation is highly active in quiescent oocytes invariably become repressed during meiotic re-entry, whereas transcripts repressed in quiescent oocytes become activated. Experimentally, we have defined the exact timing of the switch and the repressive function of CPE elements, and identified a novel role for CPEB1 in maintaining constitutive translation of a large group of maternal mRNAs during maturation.