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

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.

Automated summary

The study found that DPPA2 and DPPA4 play important roles in establishing the 2C-like state in mouse embryonic stem cells, but these factors are not essential for Dux activation, ZGA, and pre-implantation development. Therefore, caution should be taken when using 2C-like cells as a model system for studying ZGA and totipotency due to differences in regulation of two-cell embryo-specific genes compared to two-cell embryos.