Inhibition of Cell Division and DNA Replication Impair Mouse-Naïve Pluripotency Exit

The cell cycle has gained attention as a key determinant for cell fate decisions, but the contribution of DNA replication and mitosis in stem cell differentiation has not been extensively studied. To understand if these processes act as “windows of opportunity” for changes in cell identity, we estab...

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Autores principales: Waisman, Ariel, Cosentino, María Soledad, Barañao, José Lino S., Guberman, Alejandra Sonia
Publicado: 2017
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00222836_v429_n18_p2802_Waisman
http://hdl.handle.net/20.500.12110/paper_00222836_v429_n18_p2802_Waisman
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spelling paper:paper_00222836_v429_n18_p2802_Waisman2023-06-08T14:48:46Z Inhibition of Cell Division and DNA Replication Impair Mouse-Naïve Pluripotency Exit Waisman, Ariel Cosentino, María Soledad Barañao, José Lino S. Guberman, Alejandra Sonia cell division DNA replication mouse embryonic stem cells introduction primitive ectoderm-like cells DNA methyltransferase 3A kruppel like factor 4 octamer transcription factor 6 protein p53 transcription factor NANOG transcription factor Otx2 animal cell Article cell cycle cell cycle G1 phase cell cycle regulation cell cycle S phase cell differentiation cell division controlled study DNA replication mitosis mouse mouse embryonic stem cell nonhuman pluripotent stem cell priority journal stem cell animal cell differentiation genetic transcription physiology pluripotent stem cell Animals Cell Differentiation Cell Division DNA Replication Mice Mouse Embryonic Stem Cells Pluripotent Stem Cells Transcription, Genetic The cell cycle has gained attention as a key determinant for cell fate decisions, but the contribution of DNA replication and mitosis in stem cell differentiation has not been extensively studied. To understand if these processes act as “windows of opportunity” for changes in cell identity, we established synchronized cultures of mouse embryonic stem cells as they exit the ground state of pluripotency. We show that initial transcriptional changes in this transition do not require passage through mitosis and that conversion to primed pluripotency is linked to lineage priming in the G1 phase. Importantly, we demonstrate that impairment of DNA replication severely blocks transcriptional switch to primed pluripotency, even in the absence of p53 activity induced by the DNA damage response. Our data suggest an important role for DNA replication during mouse embryonic stem cell differentiation, which could shed light on why pluripotent cells are only receptive to differentiation signals during G1, that is, before the S phase. © 2017 Elsevier Ltd Fil:Waisman, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Cosentino, M.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Barañao, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Guberman, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2017 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00222836_v429_n18_p2802_Waisman http://hdl.handle.net/20.500.12110/paper_00222836_v429_n18_p2802_Waisman
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic cell division
DNA replication
mouse embryonic stem cells introduction
primitive ectoderm-like cells
DNA methyltransferase 3A
kruppel like factor 4
octamer transcription factor 6
protein p53
transcription factor NANOG
transcription factor Otx2
animal cell
Article
cell cycle
cell cycle G1 phase
cell cycle regulation
cell cycle S phase
cell differentiation
cell division
controlled study
DNA replication
mitosis
mouse
mouse embryonic stem cell
nonhuman
pluripotent stem cell
priority journal
stem cell
animal
cell differentiation
genetic transcription
physiology
pluripotent stem cell
Animals
Cell Differentiation
Cell Division
DNA Replication
Mice
Mouse Embryonic Stem Cells
Pluripotent Stem Cells
Transcription, Genetic
spellingShingle cell division
DNA replication
mouse embryonic stem cells introduction
primitive ectoderm-like cells
DNA methyltransferase 3A
kruppel like factor 4
octamer transcription factor 6
protein p53
transcription factor NANOG
transcription factor Otx2
animal cell
Article
cell cycle
cell cycle G1 phase
cell cycle regulation
cell cycle S phase
cell differentiation
cell division
controlled study
DNA replication
mitosis
mouse
mouse embryonic stem cell
nonhuman
pluripotent stem cell
priority journal
stem cell
animal
cell differentiation
genetic transcription
physiology
pluripotent stem cell
Animals
Cell Differentiation
Cell Division
DNA Replication
Mice
Mouse Embryonic Stem Cells
Pluripotent Stem Cells
Transcription, Genetic
Waisman, Ariel
Cosentino, María Soledad
Barañao, José Lino S.
Guberman, Alejandra Sonia
Inhibition of Cell Division and DNA Replication Impair Mouse-Naïve Pluripotency Exit
topic_facet cell division
DNA replication
mouse embryonic stem cells introduction
primitive ectoderm-like cells
DNA methyltransferase 3A
kruppel like factor 4
octamer transcription factor 6
protein p53
transcription factor NANOG
transcription factor Otx2
animal cell
Article
cell cycle
cell cycle G1 phase
cell cycle regulation
cell cycle S phase
cell differentiation
cell division
controlled study
DNA replication
mitosis
mouse
mouse embryonic stem cell
nonhuman
pluripotent stem cell
priority journal
stem cell
animal
cell differentiation
genetic transcription
physiology
pluripotent stem cell
Animals
Cell Differentiation
Cell Division
DNA Replication
Mice
Mouse Embryonic Stem Cells
Pluripotent Stem Cells
Transcription, Genetic
description The cell cycle has gained attention as a key determinant for cell fate decisions, but the contribution of DNA replication and mitosis in stem cell differentiation has not been extensively studied. To understand if these processes act as “windows of opportunity” for changes in cell identity, we established synchronized cultures of mouse embryonic stem cells as they exit the ground state of pluripotency. We show that initial transcriptional changes in this transition do not require passage through mitosis and that conversion to primed pluripotency is linked to lineage priming in the G1 phase. Importantly, we demonstrate that impairment of DNA replication severely blocks transcriptional switch to primed pluripotency, even in the absence of p53 activity induced by the DNA damage response. Our data suggest an important role for DNA replication during mouse embryonic stem cell differentiation, which could shed light on why pluripotent cells are only receptive to differentiation signals during G1, that is, before the S phase. © 2017 Elsevier Ltd
author Waisman, Ariel
Cosentino, María Soledad
Barañao, José Lino S.
Guberman, Alejandra Sonia
author_facet Waisman, Ariel
Cosentino, María Soledad
Barañao, José Lino S.
Guberman, Alejandra Sonia
author_sort Waisman, Ariel
title Inhibition of Cell Division and DNA Replication Impair Mouse-Naïve Pluripotency Exit
title_short Inhibition of Cell Division and DNA Replication Impair Mouse-Naïve Pluripotency Exit
title_full Inhibition of Cell Division and DNA Replication Impair Mouse-Naïve Pluripotency Exit
title_fullStr Inhibition of Cell Division and DNA Replication Impair Mouse-Naïve Pluripotency Exit
title_full_unstemmed Inhibition of Cell Division and DNA Replication Impair Mouse-Naïve Pluripotency Exit
title_sort inhibition of cell division and dna replication impair mouse-naïve pluripotency exit
publishDate 2017
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00222836_v429_n18_p2802_Waisman
http://hdl.handle.net/20.500.12110/paper_00222836_v429_n18_p2802_Waisman
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AT cosentinomariasoledad inhibitionofcelldivisionanddnareplicationimpairmousenaivepluripotencyexit
AT baranaojoselinos inhibitionofcelldivisionanddnareplicationimpairmousenaivepluripotencyexit
AT gubermanalejandrasonia inhibitionofcelldivisionanddnareplicationimpairmousenaivepluripotencyexit
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