CPEB3 Maintains Developmental Competence of the Oocyte

Author:

Lamacova Lucie1,Jansova Denisa1ORCID,Jiang Zongliang2ORCID,Dvoran Michal1ORCID,Aleshkina Daria1ORCID,Iyyappan Rajan1,Jindrova Anna1,Fan Heng-Yu3,Jiao Yuxuan3,Susor Andrej1ORCID

Affiliation:

1. Laboratory of Biochemistry and Molecular Biology of Germ Cells, IAPG CAS, Rumburska 89, 277 21 Libechov, Czech Republic

2. Department of Animal Sciences, Genetics Institute, University of Florida, Gainesville, FL 32610, USA

3. Life Sciences Institute, Zhejiang University, Hangzhou 310058, China

Abstract

Mammalian oocyte development depends on the temporally controlled translation of maternal transcripts, particularly in the coordination of meiotic and early embryonic development when transcription has ceased. The translation of mRNA is regulated by various RNA-binding proteins. We show that the absence of cytoplasmic polyadenylation element-binding protein 3 (CPEB3) negatively affects female reproductive fitness. CPEB3-depleted oocytes undergo meiosis normally but experience early embryonic arrest due to a disrupted transcriptome, leading to aberrant protein expression and the subsequent failure of embryonic transcription initiation. We found that CPEB3 stabilizes a subset of mRNAs with a significantly longer 3’UTR that is enriched in its distal region with cytoplasmic polyadenylation elements. Overall, our results suggest that CPEB3 is an important maternal factor that regulates the stability and translation of a subclass of mRNAs that are essential for the initiation of embryonic transcription and thus for embryonic development.

Funder

Institutional Research Concept

The Czech Science Foundation

NIH Eunice Kennedy Shriver National Institute of Child Health and Human Development

USDA National Institute of Food and Agriculture

Publisher

MDPI AG

Reference77 articles.

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