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Bioinformatic analysis of the four transcription factors used to induce pluripotent stem cells

Induced pluripotent stem (iPS) cells are a type of pluripotent stem cell artificially derived from non-pluripotent cells by overexpressing the transcription factors Oct4, Sox2, Klf4 and Nanog. These transcription factors play a pivotal role in stem cells; however, the function of these factors are n...

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Autores principales: Ma, Yuzhen, Zhang, Xinmin, Ma, Heping, Ren, Yu, Sun, Yangyang, Wang, Qinglian, Shi, Jingyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235945/
https://www.ncbi.nlm.nih.gov/pubmed/24129607
http://dx.doi.org/10.1007/s10616-013-9649-0
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author Ma, Yuzhen
Zhang, Xinmin
Ma, Heping
Ren, Yu
Sun, Yangyang
Wang, Qinglian
Shi, Jingyu
author_facet Ma, Yuzhen
Zhang, Xinmin
Ma, Heping
Ren, Yu
Sun, Yangyang
Wang, Qinglian
Shi, Jingyu
author_sort Ma, Yuzhen
collection PubMed
description Induced pluripotent stem (iPS) cells are a type of pluripotent stem cell artificially derived from non-pluripotent cells by overexpressing the transcription factors Oct4, Sox2, Klf4 and Nanog. These transcription factors play a pivotal role in stem cells; however, the function of these factors are not fully characterized. In this study, we analyzed Oct4, Sox2, Klf4 and Nanog in ten different species using bioinformatics, to provide more knowledge of the function of these genes. Nanog does not exist in the invertebrates Caenorhabditis elegans and Drosophila melanogaster, indicating that the absence of Nanog may be responsible for the developmental differences between vertebrates and invertebrates. Construction of phylogenetic trees confirmed that the function of Nanog is conserved from fish to mammals. The effect of alternative splicing on the protein domains present in Oct4, Sox2, Klf4 and Nanog were also analyzed. Examination of the expression patterns in human stem cells, iPS cells and normal tissues showed that Oct4, Sox2, Klf4 and Nanog are expressed at similar levels in iPS cells and embryonic stem cells, and expression of all four transcription factors decreases after differentiation. Expression of Klf4 reduced to the least during differentiation, and Klf4 was found to be specifically expressed in several normal tissues, especially the salivary gland. In this paper, we systematically indentified the family proteins of the four transcription factors used to induce pluripotent stem cells, and then analyzed their evolution status, composed of those protein domains, alternative splicing translation, expression status and interaction networks. Those analysis could shed a light for further research of iPS.
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spelling pubmed-42359452014-11-20 Bioinformatic analysis of the four transcription factors used to induce pluripotent stem cells Ma, Yuzhen Zhang, Xinmin Ma, Heping Ren, Yu Sun, Yangyang Wang, Qinglian Shi, Jingyu Cytotechnology Original Research Induced pluripotent stem (iPS) cells are a type of pluripotent stem cell artificially derived from non-pluripotent cells by overexpressing the transcription factors Oct4, Sox2, Klf4 and Nanog. These transcription factors play a pivotal role in stem cells; however, the function of these factors are not fully characterized. In this study, we analyzed Oct4, Sox2, Klf4 and Nanog in ten different species using bioinformatics, to provide more knowledge of the function of these genes. Nanog does not exist in the invertebrates Caenorhabditis elegans and Drosophila melanogaster, indicating that the absence of Nanog may be responsible for the developmental differences between vertebrates and invertebrates. Construction of phylogenetic trees confirmed that the function of Nanog is conserved from fish to mammals. The effect of alternative splicing on the protein domains present in Oct4, Sox2, Klf4 and Nanog were also analyzed. Examination of the expression patterns in human stem cells, iPS cells and normal tissues showed that Oct4, Sox2, Klf4 and Nanog are expressed at similar levels in iPS cells and embryonic stem cells, and expression of all four transcription factors decreases after differentiation. Expression of Klf4 reduced to the least during differentiation, and Klf4 was found to be specifically expressed in several normal tissues, especially the salivary gland. In this paper, we systematically indentified the family proteins of the four transcription factors used to induce pluripotent stem cells, and then analyzed their evolution status, composed of those protein domains, alternative splicing translation, expression status and interaction networks. Those analysis could shed a light for further research of iPS. Springer Netherlands 2013-10-16 2014-12 /pmc/articles/PMC4235945/ /pubmed/24129607 http://dx.doi.org/10.1007/s10616-013-9649-0 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Research
Ma, Yuzhen
Zhang, Xinmin
Ma, Heping
Ren, Yu
Sun, Yangyang
Wang, Qinglian
Shi, Jingyu
Bioinformatic analysis of the four transcription factors used to induce pluripotent stem cells
title Bioinformatic analysis of the four transcription factors used to induce pluripotent stem cells
title_full Bioinformatic analysis of the four transcription factors used to induce pluripotent stem cells
title_fullStr Bioinformatic analysis of the four transcription factors used to induce pluripotent stem cells
title_full_unstemmed Bioinformatic analysis of the four transcription factors used to induce pluripotent stem cells
title_short Bioinformatic analysis of the four transcription factors used to induce pluripotent stem cells
title_sort bioinformatic analysis of the four transcription factors used to induce pluripotent stem cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235945/
https://www.ncbi.nlm.nih.gov/pubmed/24129607
http://dx.doi.org/10.1007/s10616-013-9649-0
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