Asymmetric RBBP7 regulates the first cell fate decision of early mammalian embryos

Asymmetric transcription of noncoding RNA LincGET is currently recognized as the earliest event regulating the first cell fate decision in mammalian embryogenesis. However, whether key protein factors modulate this process remains elusive. Here, we identify RBBP7 as the earliest protein factor regulating developmental cell fate in mammals. Loss of RBBP7 drives cells towards ICM lineage. In mouse late 2-cell embryos, unequal translation of Rbbp7 contributes to its asymmetric protein distribution, which subsequently induces inversed asymmetric histone acetylation H3K9ac by interaction with HDAC1, thereby promoting cell differentiation. Interestingly, RBBP7 and LincGET exhibit a consistent asymmetric tendency but direct different cell fates; depletion or overexpression of both Rbbp7 and LincGET restored the cell fate bias, suggesting a coordinated regulatory mechanism during initial lineage specification. In summary, our study reveals RBBP7 as a new protein factor and elucidates its role in the first cell fate decision.

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Publication Details

Journal
Cell Discovery
Published
2026-08-18
DOI
https://doi.org/10.1038/s41421-026-00912-6
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Asymmetric RBBP7 regulates the first cell fate decision of early mammalian embryos

Dangsheng Li, Chun‐Chun Gao, Danru Zhang, Xiu‐Jie Wang et al.
Cell Discovery
Pluripotent Stem Cells Research
article

Asymmetric RBBP7 regulates the first cell fate decision of early mammalian embryos

Dangsheng Li, Chun‐Chun Gao, Danru Zhang, Xiu‐Jie Wang, Ying Yang, Yun‐Gui Yang, Jianyong Han, Heng-Ji Xu, Yajing Hao, Yongliang Zhao, Lin-Fang Ju, Yanchen Liu, Yusheng Chen, Meng-Xia Liu, Yu-Ting Cai, Shaokang Jia, Xiang Zhou, Xiao Han
article en

Abstract

Asymmetric transcription of noncoding RNA LincGET is currently recognized as the earliest event regulating the first cell fate decision in mammalian embryogenesis. However, whether key protein factors modulate this process remains elusive. Here, we identify RBBP7 as the earliest protein factor regulating developmental cell fate in mammals. Loss of RBBP7 drives cells towards ICM lineage. In mouse late 2-cell embryos, unequal translation of Rbbp7 contributes to its asymmetric protein distribution, which subsequently induces inversed asymmetric histone acetylation H3K9ac by interaction with HDAC1, thereby promoting cell differentiation. Interestingly, RBBP7 and LincGET exhibit a consistent asymmetric tendency but direct different cell fates; depletion or overexpression of both Rbbp7 and LincGET restored the cell fate bias, suggesting a coordinated regulatory mechanism during initial lineage specification. In summary, our study reveals RBBP7 as a new protein factor and elucidates its role in the first cell fate decision.

Cell DiscoveryVol. 12(1)
Shandong University of Technology (CN), Chinese Academy of Sciences (CN), Beijing Institute of Genomics (CN), Wuhan University (CN), Sino-Danish Centre for Education and Research (CN), China National Biotechnology (China) (CN), Center for Excellence in Molecular Cell Science (CN), Institute of Genetics and Developmental Biology (CN), University of Chinese Academy of Sciences (CN), China Agricultural University (CN), Chinese Academy of Governance (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, China Postdoctoral Science Foundation, Youth Innovation Promotion Association, Institute of Biophysics, Chinese Academy of Sciences
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Openalex Percentile: Top 16%
Pluripotent Stem Cells Research
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