DPPA2 and DPPA4 are dispensable for mouse zygotic genome activation and pre-implantation development

Author:

Chen Zhiyuan123ORCID,Xie Zhenfei123,Zhang Yi12345ORCID

Affiliation:

1. Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts 02115, USA

2. Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, Massachusetts 02115, USA

3. Division of Hematology/Oncology, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts 02115, USA

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

5. Harvard Stem Cell Institute, WAB-149G, 200 Longwood Avenue, Boston, Massachusetts 02115, USA

Abstract

ABSTRACT How maternal factors in oocytes initiate zygotic genome activation (ZGA) remains elusive in mammals, partly due to the challenge of de novo identification of key factors using scarce materials. Two-cell (2C)-like cells have been widely used as an in vitro model in order to understand mouse ZGA and totipotency because of their expression of a group of two-cell embryo-specific genes and their simplicity for genetic manipulation. Recent studies indicate that DPPA2 and DPPA4 are required for establishing the 2C-like state in mouse embryonic stem cells in a DUX-dependent manner. These results suggest that DPPA2 and DPPA4 are essential maternal factors that regulate Dux and ZGA in embryos. By analyzing maternal knockout and maternal-zygotic knockout embryos, we unexpectedly found that DPPA2 and DPPA4 are dispensable for Dux activation, ZGA and pre-implantation development. Our study suggests that 2C-like cells do not fully recapitulate two-cell embryos in terms of regulation of two-cell embryo-specific genes, and, therefore, caution should be taken when studying ZGA and totipotency using 2C-like cells as the model system.

Funder

National Institutes of Health

Howard Hughes Medical Institute

National Institute of Child Health and Human Development

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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