The PRC2-associated factor EPOP is required for Hox gene regulation during axial development in mice

The Polycomb repressive complex 2 (PRC2) is an essential modulator of gene repression. We previously reported that, in mouse embryonic stem cells, PRC2 associates with elonginB/C through EPOP, which allows for low-level expression of target genes. Here we investigate the role of EPOP in vivo by generating a mouse knockout (KO) model. We show that Epop KO mice are viable and fertile but display highly penetrant posterior homeotic transformations of the axial skeleton, which can be partially recapitulated by deletion of only the maternal allele. Epop-depleted embryos present a shift of the anterior boundary of expression of certain Hox genes. Tissue-specific RNA sequencing of embryos suggests that the Hox activation defect originates at the level of the presomitic mesoderm. Overall, we find that EPOP prevents premature activation of a subset of Hox genes, and that this is required for correct body patterning along the antero-posterior axis.

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Journal
Developmental Biology
Published
2025-08-18
DOI
https://doi.org/10.1016/j.ydbio.2025.08.014
Primary Topic
Ubiquitin and proteasome pathways
Type
article
Field-Weighted Citation Impact
0.00

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article

The PRC2-associated factor EPOP is required for Hox gene regulation during axial development in mice

Anna Mallol, Ivano Mocavini, André Dias, Luciano Di Croce et al.
Developmental Biology
Ubiquitin and proteasome pathways
article

The PRC2-associated factor EPOP is required for Hox gene regulation during axial development in mice

Anna Mallol, Ivano Mocavini, André Dias, Luciano Di Croce, Enrique Blanco, Ignacio Arce, Paul Chammas, Ana Carretero, Bernhard Payer, Arantxa Gutiérrez, Moisés Mallo
article en

Abstract

The Polycomb repressive complex 2 (PRC2) is an essential modulator of gene repression. We previously reported that, in mouse embryonic stem cells, PRC2 associates with elonginB/C through EPOP, which allows for low-level expression of target genes. Here we investigate the role of EPOP in vivo by generating a mouse knockout (KO) model. We show that Epop KO mice are viable and fertile but display highly penetrant posterior homeotic transformations of the axial skeleton, which can be partially recapitulated by deletion of only the maternal allele. Epop-depleted embryos present a shift of the anterior boundary of expression of certain Hox genes. Tissue-specific RNA sequencing of embryos suggests that the Hox activation defect originates at the level of the presomitic mesoderm. Overall, we find that EPOP prevents premature activation of a subset of Hox genes, and that this is required for correct body patterning along the antero-posterior axis.

Developmental BiologyVol. 527
Universitat Autònoma de Barcelona (ES), Universitat Pompeu Fabra (ES), Barcelona Biomedical Research Park (ES), Escola Superior de Saúde Egas Moniz (PT), Hospital de Egas Moniz (PT), Barcelona Institute of Science and Technology (ES), Centre for Genomic Regulation (ES)
Centres de Recerca de Catalunya, Generalitat de Catalunya, Ministerio de Ciencia e Innovación, Ministerio de Asuntos Económicos y Transformación Digital, Gobierno de España, Agència de Gestió d'Ajuts Universitaris i de Recerca, European Regional Development Fund, Agencia Estatal de Investigación
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Ubiquitin and proteasome pathways
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