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YY2 in Mouse Preimplantation Embryos and in Embryonic Stem Cells

Yin Yang 2 encodes a mammalian-specific transcription factor (YY2) that shares high homology in the zinc finger region with both YY1 and REX1/ZFP42, encoded by the Yin Yang 1 and Reduced Expression Protein 1/Zinc Finger Protein 42 gene, respectively. In contrast to the well-established roles of the...

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Autores principales: Pérez-Palacios, Raquel, Climent, María, Santiago-Arcos, Javier, Macías-Redondo, Sofía, Klar, Martin, Muniesa, Pedro, Schoorlemmer, Jon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148602/
https://www.ncbi.nlm.nih.gov/pubmed/34066930
http://dx.doi.org/10.3390/cells10051123
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author Pérez-Palacios, Raquel
Climent, María
Santiago-Arcos, Javier
Macías-Redondo, Sofía
Klar, Martin
Muniesa, Pedro
Schoorlemmer, Jon
author_facet Pérez-Palacios, Raquel
Climent, María
Santiago-Arcos, Javier
Macías-Redondo, Sofía
Klar, Martin
Muniesa, Pedro
Schoorlemmer, Jon
author_sort Pérez-Palacios, Raquel
collection PubMed
description Yin Yang 2 encodes a mammalian-specific transcription factor (YY2) that shares high homology in the zinc finger region with both YY1 and REX1/ZFP42, encoded by the Yin Yang 1 and Reduced Expression Protein 1/Zinc Finger Protein 42 gene, respectively. In contrast to the well-established roles of the latter two in gene regulation, X chromosome inactivation and binding to specific transposable elements (TEs), much less is known about YY2, and its presence during mouse preimplantation development has not been described. As it has been reported that mouse embryonic stem cells (mESC) cannot be propagated in the absence of Yy2, the mechanistic understanding of how Yy2 contributes to mESC maintenance remains only very partially characterized. We describe Yy2 expression studies using RT-PCR and staining with a high-affinity polyclonal serum in mouse embryos and mESC. Although YY2 is expressed during preimplantation development, its presence appears dispensable for developmental progress in vitro until formation of the blastocyst. Attenuation of Yy2 levels failed to alter either Zscan4 levels in two-cell embryos or IAP and MERVL levels at later preimplantation stages. In contrast to previous claims that constitutively expressed shRNA against Yy2 in mESC prohibited the propagation of mESC in culture, we obtained colonies generated from mESC with attenuated Yy2 levels. Concomitant with a decreased number of undifferentiated colonies, Yy2-depleted mESC expressed higher levels of Zscan4 but no differences in the expression of TEs or other pluripotency markers including Sox2, Oct4, Nanog and Esrrb were observed. These results confirm the contribution of Yy2 to the maintenance of mouse embryonic stem cells and show the preimplantation expression of YY2. These functions are discussed in relation to mammalian-specific functions of YY1 and REX1.
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spelling pubmed-81486022021-05-26 YY2 in Mouse Preimplantation Embryos and in Embryonic Stem Cells Pérez-Palacios, Raquel Climent, María Santiago-Arcos, Javier Macías-Redondo, Sofía Klar, Martin Muniesa, Pedro Schoorlemmer, Jon Cells Article Yin Yang 2 encodes a mammalian-specific transcription factor (YY2) that shares high homology in the zinc finger region with both YY1 and REX1/ZFP42, encoded by the Yin Yang 1 and Reduced Expression Protein 1/Zinc Finger Protein 42 gene, respectively. In contrast to the well-established roles of the latter two in gene regulation, X chromosome inactivation and binding to specific transposable elements (TEs), much less is known about YY2, and its presence during mouse preimplantation development has not been described. As it has been reported that mouse embryonic stem cells (mESC) cannot be propagated in the absence of Yy2, the mechanistic understanding of how Yy2 contributes to mESC maintenance remains only very partially characterized. We describe Yy2 expression studies using RT-PCR and staining with a high-affinity polyclonal serum in mouse embryos and mESC. Although YY2 is expressed during preimplantation development, its presence appears dispensable for developmental progress in vitro until formation of the blastocyst. Attenuation of Yy2 levels failed to alter either Zscan4 levels in two-cell embryos or IAP and MERVL levels at later preimplantation stages. In contrast to previous claims that constitutively expressed shRNA against Yy2 in mESC prohibited the propagation of mESC in culture, we obtained colonies generated from mESC with attenuated Yy2 levels. Concomitant with a decreased number of undifferentiated colonies, Yy2-depleted mESC expressed higher levels of Zscan4 but no differences in the expression of TEs or other pluripotency markers including Sox2, Oct4, Nanog and Esrrb were observed. These results confirm the contribution of Yy2 to the maintenance of mouse embryonic stem cells and show the preimplantation expression of YY2. These functions are discussed in relation to mammalian-specific functions of YY1 and REX1. MDPI 2021-05-07 /pmc/articles/PMC8148602/ /pubmed/34066930 http://dx.doi.org/10.3390/cells10051123 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pérez-Palacios, Raquel
Climent, María
Santiago-Arcos, Javier
Macías-Redondo, Sofía
Klar, Martin
Muniesa, Pedro
Schoorlemmer, Jon
YY2 in Mouse Preimplantation Embryos and in Embryonic Stem Cells
title YY2 in Mouse Preimplantation Embryos and in Embryonic Stem Cells
title_full YY2 in Mouse Preimplantation Embryos and in Embryonic Stem Cells
title_fullStr YY2 in Mouse Preimplantation Embryos and in Embryonic Stem Cells
title_full_unstemmed YY2 in Mouse Preimplantation Embryos and in Embryonic Stem Cells
title_short YY2 in Mouse Preimplantation Embryos and in Embryonic Stem Cells
title_sort yy2 in mouse preimplantation embryos and in embryonic stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148602/
https://www.ncbi.nlm.nih.gov/pubmed/34066930
http://dx.doi.org/10.3390/cells10051123
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