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Zscan4 Is Activated after Telomere Shortening in Mouse Embryonic Stem Cells

ZSCAN4 is a DNA-binding protein that functions for telomere elongation and genomic stability. In vivo, it is specifically expressed at the two-cell stage during mouse development. In vitro, it is transiently expressed in mouse embryonic stem cells (ESCs), only in 5% of the population at one time. He...

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Detalles Bibliográficos
Autores principales: Nakai-Futatsugi, Yoko, Niwa, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834046/
https://www.ncbi.nlm.nih.gov/pubmed/26997646
http://dx.doi.org/10.1016/j.stemcr.2016.02.010
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author Nakai-Futatsugi, Yoko
Niwa, Hitoshi
author_facet Nakai-Futatsugi, Yoko
Niwa, Hitoshi
author_sort Nakai-Futatsugi, Yoko
collection PubMed
description ZSCAN4 is a DNA-binding protein that functions for telomere elongation and genomic stability. In vivo, it is specifically expressed at the two-cell stage during mouse development. In vitro, it is transiently expressed in mouse embryonic stem cells (ESCs), only in 5% of the population at one time. Here we attempted to elucidate when, under what circumstances, Zscan4 is activated in ESCs. Using live cell imaging, we monitored the activity of Zscan4 together with the pluripotency marker Rex1. The lengths of the cell cycles in ESCs were diverse. Longer cell cycles were accompanied by shorter telomeres and higher activation of Zscan4. Since activation of Zscan4 is involved in telomere elongation, we speculate that the extended cell cycles accompanied by Zscan4 activation reflect the time for telomere recovery. Rex1 and Zscan4 did not show any correlation. Taken together, we propose that Zscan4 is activated to recover shortened telomeres during extended cell cycles, irrespective of the pluripotent status.
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spelling pubmed-48340462016-04-27 Zscan4 Is Activated after Telomere Shortening in Mouse Embryonic Stem Cells Nakai-Futatsugi, Yoko Niwa, Hitoshi Stem Cell Reports Article ZSCAN4 is a DNA-binding protein that functions for telomere elongation and genomic stability. In vivo, it is specifically expressed at the two-cell stage during mouse development. In vitro, it is transiently expressed in mouse embryonic stem cells (ESCs), only in 5% of the population at one time. Here we attempted to elucidate when, under what circumstances, Zscan4 is activated in ESCs. Using live cell imaging, we monitored the activity of Zscan4 together with the pluripotency marker Rex1. The lengths of the cell cycles in ESCs were diverse. Longer cell cycles were accompanied by shorter telomeres and higher activation of Zscan4. Since activation of Zscan4 is involved in telomere elongation, we speculate that the extended cell cycles accompanied by Zscan4 activation reflect the time for telomere recovery. Rex1 and Zscan4 did not show any correlation. Taken together, we propose that Zscan4 is activated to recover shortened telomeres during extended cell cycles, irrespective of the pluripotent status. Elsevier 2016-03-17 /pmc/articles/PMC4834046/ /pubmed/26997646 http://dx.doi.org/10.1016/j.stemcr.2016.02.010 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nakai-Futatsugi, Yoko
Niwa, Hitoshi
Zscan4 Is Activated after Telomere Shortening in Mouse Embryonic Stem Cells
title Zscan4 Is Activated after Telomere Shortening in Mouse Embryonic Stem Cells
title_full Zscan4 Is Activated after Telomere Shortening in Mouse Embryonic Stem Cells
title_fullStr Zscan4 Is Activated after Telomere Shortening in Mouse Embryonic Stem Cells
title_full_unstemmed Zscan4 Is Activated after Telomere Shortening in Mouse Embryonic Stem Cells
title_short Zscan4 Is Activated after Telomere Shortening in Mouse Embryonic Stem Cells
title_sort zscan4 is activated after telomere shortening in mouse embryonic stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834046/
https://www.ncbi.nlm.nih.gov/pubmed/26997646
http://dx.doi.org/10.1016/j.stemcr.2016.02.010
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