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Global transcriptome analysis of pig induced pluripotent stem cells derived from six and four reprogramming factors

Pigs are important, both for agriculture and as animal models for human diseases. However, due to the lack of embryonic stem cells, the possibility of genetic modification is quite limited. To overcome this limitation, induced pluripotent stem (iPS) cells have been derived from pigs. Despite the pub...

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Autores principales: Fukuda, Tomokazu, Doi, Koji, Donai, Kenichiro, Takahashi, Kouhei, Kobayashi, Hisato, Hirano, Takashi, Nishimori, Katsuhiko, Yasue, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390709/
https://www.ncbi.nlm.nih.gov/pubmed/30806635
http://dx.doi.org/10.1038/sdata.2019.34
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author Fukuda, Tomokazu
Doi, Koji
Donai, Kenichiro
Takahashi, Kouhei
Kobayashi, Hisato
Hirano, Takashi
Nishimori, Katsuhiko
Yasue, Hiroshi
author_facet Fukuda, Tomokazu
Doi, Koji
Donai, Kenichiro
Takahashi, Kouhei
Kobayashi, Hisato
Hirano, Takashi
Nishimori, Katsuhiko
Yasue, Hiroshi
author_sort Fukuda, Tomokazu
collection PubMed
description Pigs are important, both for agriculture and as animal models for human diseases. However, due to the lack of embryonic stem cells, the possibility of genetic modification is quite limited. To overcome this limitation, induced pluripotent stem (iPS) cells have been derived from pigs. Despite the public availability of a large number of expression datasets from mice, rats, and primates-derived iPS cells, the expression profile of pig-derived iPS cells is quite limited. Furthermore, there is no dataset focused on the profiling of pig-derived iPS cell with six reprogramming factors (Oct3/4, Sox2, Klf4, c-Myc, Lin28, and Nanog). Here, we used Illumina RNA sequencing platform to characterize the mRNA expression of four-factor derived and six-factor derived pig iPS cells. We observed that the expression levels of whole genes in our established six factors derived iPS cells and parent fibroblast, and compared with that of iPS cells with four factors in public database. These data are valuable in understanding species difference in the reprogramming process of stem cells, and could help identify the key regulating genes involved in the process.
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spelling pubmed-63907092019-02-27 Global transcriptome analysis of pig induced pluripotent stem cells derived from six and four reprogramming factors Fukuda, Tomokazu Doi, Koji Donai, Kenichiro Takahashi, Kouhei Kobayashi, Hisato Hirano, Takashi Nishimori, Katsuhiko Yasue, Hiroshi Sci Data Data Descriptor Pigs are important, both for agriculture and as animal models for human diseases. However, due to the lack of embryonic stem cells, the possibility of genetic modification is quite limited. To overcome this limitation, induced pluripotent stem (iPS) cells have been derived from pigs. Despite the public availability of a large number of expression datasets from mice, rats, and primates-derived iPS cells, the expression profile of pig-derived iPS cells is quite limited. Furthermore, there is no dataset focused on the profiling of pig-derived iPS cell with six reprogramming factors (Oct3/4, Sox2, Klf4, c-Myc, Lin28, and Nanog). Here, we used Illumina RNA sequencing platform to characterize the mRNA expression of four-factor derived and six-factor derived pig iPS cells. We observed that the expression levels of whole genes in our established six factors derived iPS cells and parent fibroblast, and compared with that of iPS cells with four factors in public database. These data are valuable in understanding species difference in the reprogramming process of stem cells, and could help identify the key regulating genes involved in the process. Nature Publishing Group 2019-02-26 /pmc/articles/PMC6390709/ /pubmed/30806635 http://dx.doi.org/10.1038/sdata.2019.34 Text en Copyright © 2019, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ The Creative Commons Public Domain Dedication waiver http://creativecommons.org/publicdomain/zero/1.0/ applies to the metadata files made available in this article.
spellingShingle Data Descriptor
Fukuda, Tomokazu
Doi, Koji
Donai, Kenichiro
Takahashi, Kouhei
Kobayashi, Hisato
Hirano, Takashi
Nishimori, Katsuhiko
Yasue, Hiroshi
Global transcriptome analysis of pig induced pluripotent stem cells derived from six and four reprogramming factors
title Global transcriptome analysis of pig induced pluripotent stem cells derived from six and four reprogramming factors
title_full Global transcriptome analysis of pig induced pluripotent stem cells derived from six and four reprogramming factors
title_fullStr Global transcriptome analysis of pig induced pluripotent stem cells derived from six and four reprogramming factors
title_full_unstemmed Global transcriptome analysis of pig induced pluripotent stem cells derived from six and four reprogramming factors
title_short Global transcriptome analysis of pig induced pluripotent stem cells derived from six and four reprogramming factors
title_sort global transcriptome analysis of pig induced pluripotent stem cells derived from six and four reprogramming factors
topic Data Descriptor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390709/
https://www.ncbi.nlm.nih.gov/pubmed/30806635
http://dx.doi.org/10.1038/sdata.2019.34
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