OVOL1/2 regulate trophectoderm differentiation during the morula-to-blastocyst transition

The blastocyst formation rate of human embryos cultured in vitro for assisted reproduction is approximately 50%, with most embryos arresting at the cleavage stage; however, the underlying mechanisms remain poorly understood. Here, we performed single-cell RNA sequencing of biopsied blastomeres from morphologically high-quality 8-cell embryos and tracked the developmental progression of the remaining embryos to the blastocyst stage. Embryos that failed to form blastocysts exhibited impaired zygotic genome activation (ZGA). We identified OVOL1/2 as critical ZGA genes that were markedly underactivated in these embryos. Functional analyses in both mouse and human embryos demonstrate that depletion of OVOL1/2 disrupts trophectoderm differentiation via ARPC1B-dependent mechanisms, thereby impairing the morula-to-blastocyst transition. Collectively, these findings provide mechanistic insights into preimplantation embryonic development and reveal potential causes of blastocyst formation failure.

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Publication Details

Journal
Communications Biology
Published
2026-10-29
DOI
https://doi.org/10.1038/s42003-026-11168-x
Primary Topic
Reproductive Biology and Fertility
Type
article
Field-Weighted Citation Impact
0.00

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article

OVOL1/2 regulate trophectoderm differentiation during the morula-to-blastocyst transition

Yifan Gu, J Zhang, Xin Deng, Ge Lin et al.
1 links
Communications Biology
Reproductive Biology and Fertility
article

OVOL1/2 regulate trophectoderm differentiation during the morula-to-blastocyst transition

Yifan Gu, J Zhang, Xin Deng, Ge Lin, Fei Meng, Fei Gong, Yi Zhu, Guangxiu Lu, Xueqin Chen, Qinwei Zhou, Lizhi Leng, Shuoping Zhang
article en

Abstract

The blastocyst formation rate of human embryos cultured in vitro for assisted reproduction is approximately 50%, with most embryos arresting at the cleavage stage; however, the underlying mechanisms remain poorly understood. Here, we performed single-cell RNA sequencing of biopsied blastomeres from morphologically high-quality 8-cell embryos and tracked the developmental progression of the remaining embryos to the blastocyst stage. Embryos that failed to form blastocysts exhibited impaired zygotic genome activation (ZGA). We identified OVOL1/2 as critical ZGA genes that were markedly underactivated in these embryos. Functional analyses in both mouse and human embryos demonstrate that depletion of OVOL1/2 disrupts trophectoderm differentiation via ARPC1B-dependent mechanisms, thereby impairing the morula-to-blastocyst transition. Collectively, these findings provide mechanistic insights into preimplantation embryonic development and reveal potential causes of blastocyst formation failure.

Communications BiologyVol. 9(1)
Central South University (CN), Reproductive & Genetic Hospital CITIC-Xiangya (CN), National Engineering Research Center of Human Stem Cells (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hunan Province
Good health and well-being
Openalex Percentile: Top 10%
Reproductive Biology and Fertility
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OVOL1/2 regulate trophectoderm differentiation during the morula-to-blastocyst transition — Yifan Gu, J Zhang, et al. · Communications Biology (2026) | TGRS Research Map | TGRS