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β-catenin fluctuates in mouse ESCs and is essential for Nanog-mediated/nreprogramming of somatic cells to pluripotency
Identificadores del recurso
Marucci L, Pedone E, Di Vicino U, Sanuy-Escribano B, Isalan M, Cosma MP./nβ-catenin fluctuates in mouse ESCs and is essential for Nanog-mediated/nreprogramming of somatic cells to pluripotency. Cell Rep. 2014 Sep/n25;8(6):1686-96. DOI: 10.1016/j.celrep.2014.08.011
2211-1247
http://hdl.handle.net/10230/23505
http://dx.doi.org/10.1016/j.celrep.2014.08.011
Origin
(e-Repositori: Repositori digital de la UPF)

File

Title:
β-catenin fluctuates in mouse ESCs and is essential for Nanog-mediated/nreprogramming of somatic cells to pluripotency
Tema:
Cèl·lules mare
Description:
The Wnt/β-catenin pathway and Nanog are key regulators of embryonic stem cell (ESC) pluripotency and the reprogramming of somatic cells. Here, we demonstrate that the repression of Dkk1 by Nanog, which leads indirectly to β-catenin activation, is essential for reprogramming after fusion of ESCs overexpressing Nanog. In addition, β-catenin is necessary in Nanog-dependent conversion of preinduced pluripotent stem cells (pre-iPSCs) into iPSCs. The activation of β-catenin by Nanog causes fluctuations of β-catenin in ESCs cultured in serum plus leukemia inhibitory factor (serum+LIF) medium, in which protein levels of key pluripotency factors are heterogeneous. In 2i+LIF medium, which favors propagation of ESCs in a ground state of pluripotency with many pluripotency genes losing mosaic expression, we show Nanog-independent β-catenin fluctuations. Overall, we demonstrate Nanog and β-catenin cooperation in establishing naive pluripotency during the reprogramming process and their correlated heterogeneity in ESCs primed toward differentiation.
This work was funded by an ERC grant (242630-RERE) (M.P.C.), an HFSP grant (M.P.C.), the Ministerio de Ciencia e Inovación SAF2011-28580 (M.P.C.), Fundacio La Marató de TV3 (M.P.C.), AXA Research Fund (M.P.C.), an EMBO Long-Term Fellowship (L.M.), and Wolfson Foundation and BBSRC Alert 13 capital grant (BB/L014181/1) (Bristol University)
Idioma:
English
Relation:
Cell Reports. 2014 Sep/n25;8(6):1686-96
info:eu-repo/grantAgreement/EC/FP7/242630
info:eu-repo/grantAgreement/ES/3PN/SAF2011-28580
Autor/Productor:
Marucci, Lucia
Pedone, Elisa, 1985-
Vicino, Umberto di
Sanuy-Escribano, Blanca
Isalan, Mark
Cosma, Maria Pia, 1970-
Publisher:
Elsevier
Rights:
© Elsevier http://dx.doi.org/10.1016/j.celrep.2014.08.011
http://creativecommons.org/licenses/by-nc-nd/3.0/
info:eu-repo/semantics/openAccess
Date:
2014
Tipo de recurso:
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Format:
application/pdf

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            1. <field name="value">The Wnt/β-catenin pathway and Nanog are key regulators of embryonic stem cell (ESC) pluripotency and the reprogramming of somatic cells. Here, we demonstrate that the repression of Dkk1 by Nanog, which leads indirectly to β-catenin activation, is essential for reprogramming after fusion of ESCs overexpressing Nanog. In addition, β-catenin is necessary in Nanog-dependent conversion of preinduced pluripotent stem cells (pre-iPSCs) into iPSCs. The activation of β-catenin by Nanog causes fluctuations of β-catenin in ESCs cultured in serum plus leukemia inhibitory factor (serum+LIF) medium, in which protein levels of key pluripotency factors are heterogeneous. In 2i+LIF medium, which favors propagation of ESCs in a ground state of pluripotency with many pluripotency genes losing mosaic expression, we show Nanog-independent β-catenin fluctuations. Overall, we demonstrate Nanog and β-catenin cooperation in establishing naive pluripotency during the reprogramming process and their correlated heterogeneity in ESCs primed toward differentiation.</field>

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            1. <field name="value">This work was funded by an ERC grant (242630-RERE) (M.P.C.), an HFSP grant (M.P.C.), the Ministerio de Ciencia e Inovación SAF2011-28580 (M.P.C.), Fundacio La Marató de TV3 (M.P.C.), AXA Research Fund (M.P.C.), an EMBO Long-Term Fellowship (L.M.), and Wolfson Foundation and BBSRC Alert 13 capital grant (BB/L014181/1) (Bristol University)</field>

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            1. <field name="value">Cell Reports. 2014 Sep/n25;8(6):1686-96</field>

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          1. <field name="value">© Elsevier http://dx.doi.org/10.1016/j.celrep.2014.08.011</field>

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            1. <field name="value">Cèl·lules mare</field>

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