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Oocyte-Specific Homeobox 1, Obox1, Facilitates Reprogramming by Promoting Mesenchymal-to-Epithelial Transition and Mitigating Cell Hyperproliferation

Mammalian oocytes possess fascinating unknown factors, which can reprogram terminally differentiated germ cells or somatic cells into totipotent embryos. Here, we demonstrate that oocyte-specific homeobox 1 (Obox1), an oocyte-specific factor, can markedly enhance the generation of induced pluripoten...

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Autores principales: Wu, Li, Wu, You, Peng, Bing, Hou, Zhenzhen, Dong, Yu, Chen, Kang, Guo, Mingyue, Li, Han, Chen, Xia, Kou, Xiaochen, Zhao, Yanhong, Bi, Yan, Wang, Yixuan, Wang, Hong, Le, Rongrong, Kang, Lan, Gao, Shaorong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853649/
https://www.ncbi.nlm.nih.gov/pubmed/29033306
http://dx.doi.org/10.1016/j.stemcr.2017.09.012
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author Wu, Li
Wu, You
Peng, Bing
Hou, Zhenzhen
Dong, Yu
Chen, Kang
Guo, Mingyue
Li, Han
Chen, Xia
Kou, Xiaochen
Zhao, Yanhong
Bi, Yan
Wang, Yixuan
Wang, Hong
Le, Rongrong
Kang, Lan
Gao, Shaorong
author_facet Wu, Li
Wu, You
Peng, Bing
Hou, Zhenzhen
Dong, Yu
Chen, Kang
Guo, Mingyue
Li, Han
Chen, Xia
Kou, Xiaochen
Zhao, Yanhong
Bi, Yan
Wang, Yixuan
Wang, Hong
Le, Rongrong
Kang, Lan
Gao, Shaorong
author_sort Wu, Li
collection PubMed
description Mammalian oocytes possess fascinating unknown factors, which can reprogram terminally differentiated germ cells or somatic cells into totipotent embryos. Here, we demonstrate that oocyte-specific homeobox 1 (Obox1), an oocyte-specific factor, can markedly enhance the generation of induced pluripotent stem cells (iPSCs) from mouse fibroblasts in a proliferation-independent manner and can replace Sox2 to achieve pluripotency. Overexpression of Obox1 can greatly promote mesenchymal-to-epithelial transition (MET) at early stage of OSKM-induced reprogramming, and meanwhile, the hyperproliferation of THY1-positive cells can be significantly mitigated. Subsequently, the proportion of THY1-negative cells and Oct4-GFP-positive cells increased dramatically. Further analysis of gene expression and targets of Obox1 during reprogramming indicates that the expression of Obox1 can promote epithelial gene expression and modulate cell-cycle-related gene expression. Taken together, we conclude that the oocyte-specific factor Obox1 serves as a strong activator for somatic cell reprogramming through promoting the MET and mitigating cell hyperproliferation.
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spelling pubmed-58536492018-03-19 Oocyte-Specific Homeobox 1, Obox1, Facilitates Reprogramming by Promoting Mesenchymal-to-Epithelial Transition and Mitigating Cell Hyperproliferation Wu, Li Wu, You Peng, Bing Hou, Zhenzhen Dong, Yu Chen, Kang Guo, Mingyue Li, Han Chen, Xia Kou, Xiaochen Zhao, Yanhong Bi, Yan Wang, Yixuan Wang, Hong Le, Rongrong Kang, Lan Gao, Shaorong Stem Cell Reports Article Mammalian oocytes possess fascinating unknown factors, which can reprogram terminally differentiated germ cells or somatic cells into totipotent embryos. Here, we demonstrate that oocyte-specific homeobox 1 (Obox1), an oocyte-specific factor, can markedly enhance the generation of induced pluripotent stem cells (iPSCs) from mouse fibroblasts in a proliferation-independent manner and can replace Sox2 to achieve pluripotency. Overexpression of Obox1 can greatly promote mesenchymal-to-epithelial transition (MET) at early stage of OSKM-induced reprogramming, and meanwhile, the hyperproliferation of THY1-positive cells can be significantly mitigated. Subsequently, the proportion of THY1-negative cells and Oct4-GFP-positive cells increased dramatically. Further analysis of gene expression and targets of Obox1 during reprogramming indicates that the expression of Obox1 can promote epithelial gene expression and modulate cell-cycle-related gene expression. Taken together, we conclude that the oocyte-specific factor Obox1 serves as a strong activator for somatic cell reprogramming through promoting the MET and mitigating cell hyperproliferation. Elsevier 2017-10-12 /pmc/articles/PMC5853649/ /pubmed/29033306 http://dx.doi.org/10.1016/j.stemcr.2017.09.012 Text en © 2017 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
Wu, Li
Wu, You
Peng, Bing
Hou, Zhenzhen
Dong, Yu
Chen, Kang
Guo, Mingyue
Li, Han
Chen, Xia
Kou, Xiaochen
Zhao, Yanhong
Bi, Yan
Wang, Yixuan
Wang, Hong
Le, Rongrong
Kang, Lan
Gao, Shaorong
Oocyte-Specific Homeobox 1, Obox1, Facilitates Reprogramming by Promoting Mesenchymal-to-Epithelial Transition and Mitigating Cell Hyperproliferation
title Oocyte-Specific Homeobox 1, Obox1, Facilitates Reprogramming by Promoting Mesenchymal-to-Epithelial Transition and Mitigating Cell Hyperproliferation
title_full Oocyte-Specific Homeobox 1, Obox1, Facilitates Reprogramming by Promoting Mesenchymal-to-Epithelial Transition and Mitigating Cell Hyperproliferation
title_fullStr Oocyte-Specific Homeobox 1, Obox1, Facilitates Reprogramming by Promoting Mesenchymal-to-Epithelial Transition and Mitigating Cell Hyperproliferation
title_full_unstemmed Oocyte-Specific Homeobox 1, Obox1, Facilitates Reprogramming by Promoting Mesenchymal-to-Epithelial Transition and Mitigating Cell Hyperproliferation
title_short Oocyte-Specific Homeobox 1, Obox1, Facilitates Reprogramming by Promoting Mesenchymal-to-Epithelial Transition and Mitigating Cell Hyperproliferation
title_sort oocyte-specific homeobox 1, obox1, facilitates reprogramming by promoting mesenchymal-to-epithelial transition and mitigating cell hyperproliferation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853649/
https://www.ncbi.nlm.nih.gov/pubmed/29033306
http://dx.doi.org/10.1016/j.stemcr.2017.09.012
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