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Cell cycle and pluripotency: Convergence on octamer-binding transcription factor 4

Embryonic stem cells (ESCs) have unlimited expansion potential and the ability to differentiate into all somatic cell types for regenerative medicine and disease model studies. Octamer-binding transcription factor 4 (OCT4), encoded by the POU domain, class 5, transcription factor 1 gene, is a transc...

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Autores principales: She, Shiqi, Wei, Qucheng, Kang, Bo, Wang, Ying-Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865814/
https://www.ncbi.nlm.nih.gov/pubmed/28901500
http://dx.doi.org/10.3892/mmr.2017.7489
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author She, Shiqi
Wei, Qucheng
Kang, Bo
Wang, Ying-Jie
author_facet She, Shiqi
Wei, Qucheng
Kang, Bo
Wang, Ying-Jie
author_sort She, Shiqi
collection PubMed
description Embryonic stem cells (ESCs) have unlimited expansion potential and the ability to differentiate into all somatic cell types for regenerative medicine and disease model studies. Octamer-binding transcription factor 4 (OCT4), encoded by the POU domain, class 5, transcription factor 1 gene, is a transcription factor vital for maintaining ESC pluripotency and somatic reprogramming. Many studies have established that the cell cycle of ESCs is featured with an abbreviated G1 phase and a prolonged S phase. Changes in cell cycle dynamics are intimately associated with the state of ESC pluripotency, and manipulating cell-cycle regulators could enable a controlled differentiation of ESCs. The present review focused primarily on the emerging roles of OCT4 in coordinating the cell cycle progression, the maintenance of pluripotency and the glycolytic metabolism in ESCs.
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spelling pubmed-58658142018-03-27 Cell cycle and pluripotency: Convergence on octamer-binding transcription factor 4 She, Shiqi Wei, Qucheng Kang, Bo Wang, Ying-Jie Mol Med Rep Review Embryonic stem cells (ESCs) have unlimited expansion potential and the ability to differentiate into all somatic cell types for regenerative medicine and disease model studies. Octamer-binding transcription factor 4 (OCT4), encoded by the POU domain, class 5, transcription factor 1 gene, is a transcription factor vital for maintaining ESC pluripotency and somatic reprogramming. Many studies have established that the cell cycle of ESCs is featured with an abbreviated G1 phase and a prolonged S phase. Changes in cell cycle dynamics are intimately associated with the state of ESC pluripotency, and manipulating cell-cycle regulators could enable a controlled differentiation of ESCs. The present review focused primarily on the emerging roles of OCT4 in coordinating the cell cycle progression, the maintenance of pluripotency and the glycolytic metabolism in ESCs. D.A. Spandidos 2017-11 2017-09-13 /pmc/articles/PMC5865814/ /pubmed/28901500 http://dx.doi.org/10.3892/mmr.2017.7489 Text en Copyright: © She et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
She, Shiqi
Wei, Qucheng
Kang, Bo
Wang, Ying-Jie
Cell cycle and pluripotency: Convergence on octamer-binding transcription factor 4
title Cell cycle and pluripotency: Convergence on octamer-binding transcription factor 4
title_full Cell cycle and pluripotency: Convergence on octamer-binding transcription factor 4
title_fullStr Cell cycle and pluripotency: Convergence on octamer-binding transcription factor 4
title_full_unstemmed Cell cycle and pluripotency: Convergence on octamer-binding transcription factor 4
title_short Cell cycle and pluripotency: Convergence on octamer-binding transcription factor 4
title_sort cell cycle and pluripotency: convergence on octamer-binding transcription factor 4
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865814/
https://www.ncbi.nlm.nih.gov/pubmed/28901500
http://dx.doi.org/10.3892/mmr.2017.7489
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