VGLL1 cooperates with TEAD4 to control human trophectoderm lineage specification Journal Article


Authors: Yang, Y.; Jia, W.; Luo, Z.; Li, Y.; Liu, H.; Fu, L.; Li, J.; Jiang, Y.; Lai, J.; Li, H.; Saeed, B. J.; Zou, Y.; Lv, Y.; Wu, L.; Zhou, T.; Shan, Y.; Liu, C.; Lai, Y.; Liu, L.; Hutchins, A. P.; Esteban, M. A.; Mazid, M. A.; Li, W.
Article Title: VGLL1 cooperates with TEAD4 to control human trophectoderm lineage specification
Abstract: In contrast to rodents, the mechanisms underlying human trophectoderm and early placenta specification are understudied due to ethical barriers and the scarcity of embryos. Recent reports have shown that human pluripotent stem cells (PSCs) can differentiate into trophectoderm (TE)-like cells (TELCs) and trophoblast stem cells (TSCs), offering a valuable in vitro model to study early placenta specification. Here, we demonstrate that the VGLL1 (vestigial-like family member 1), which is highly expressed during human and non-human primate TE specification in vivo but is negligibly expressed in mouse, is a critical regulator of cell fate determination and self-renewal in human TELCs and TSCs derived from naïve PSCs. Mechanistically, VGLL1 partners with the transcription factor TEAD4 (TEA domain transcription factor 4) to regulate chromatin accessibility at target gene loci through histone acetylation and acts in cooperation with GATA3 and TFAP2C. Our work is relevant to understand primate early embryogenesis and how it differs from other mammalian species. © 2024, The Author(s).
Keywords: dna binding protein; genetics; dna-binding proteins; mouse; animal; animals; mice; gene expression; transcription factor; cell differentiation; physiology; cell lineage; transcription factors; mammal; pregnancy; pluripotent stem cell; pluripotent stem cells; primate; mammals; chemical reaction; embryonic development; trophoblast; trophoblasts; primates; cell component; humans; human; female; vgll1 protein, human; tea domain transcription factors; tea domain transcription factor; tead4 protein, human
Journal Title: Nature Communications
Volume: 15
ISSN: 2041-1723
Publisher: Nature Publishing Group  
Date Published: 2024-01-17
Start Page: 583
Language: English
DOI: 10.1038/s41467-024-44780-8
PUBMED: 38233381
PROVIDER: scopus
PMCID: PMC10794710
DOI/URL:
Notes: Erratum issued, see DOI: 10.1038/s41467-025-57929-w -- Source: Scopus
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  1. Ting Zhou
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