Profiling and functional characterization of maternal mRNA translation during mouse maternal-to-zygotic transition

Author:

Zhang Chunxia12ORCID,Wang Meng12ORCID,Li Yisi123ORCID,Zhang Yi1245ORCID

Affiliation:

1. Howard Hughes Medical Institute, Boston Children’s Hospital, Boston, MA 02115, USA.

2. Program in Cellular and Molecular Medicine, Boston Children’s Hospital, Boston, MA 02115, USA.

3. Department of Automation, Tsinghua University, Beijing 100084, China.

4. Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.

5. Harvard Stem Cell Institute, Boston, MA 02115, USA.

Abstract

Translational regulation plays an important role in gene expression and function. Although the transcriptional dynamics of mouse preimplantation embryos have been well characterized, the global mRNA translation landscape and the master regulators of zygotic genome activation (ZGA) remain unknown. Here, by developing and applying a low-input ribosome profiling (LiRibo-seq) technique, we profiled the mRNA translation landscape in mouse preimplantation embryos and revealed the translational dynamics during mouse preimplantation development. We identified a marked translational transition from MII oocytes to zygotes and demonstrated that active translation of maternal mRNAs is essential for maternal-to-zygotic transition (MZT). We further showed that two maternal factors, Smarcd2 and Cyclin T2, whose translation is activated in zygotes, are required for chromatin reprogramming and ZGA, respectively. Our study thus not only filled in a knowledge gap on translational regulation during mammalian preimplantation development but also revealed insights into the critical function of maternal mRNA translation in MZT.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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