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Generation and gene expression profiling of 48 transcription-factor-inducible mouse embryonic stem cell lines
Mouse embryonic stem cells (ESCs) can differentiate into a wide range – and possibly all cell types in vitro, and thus provide an ideal platform to study systematically the action of transcription factors (TFs) in cell differentiation. Previously, we have generated and analyzed 137 TF-inducible mous...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858678/ https://www.ncbi.nlm.nih.gov/pubmed/27150017 http://dx.doi.org/10.1038/srep25667 |
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author | Yamamizu, Kohei Sharov, Alexei A. Piao, Yulan Amano, Misa Yu, Hong Nishiyama, Akira Dudekula, Dawood B. Schlessinger, David Ko, Minoru S. H. |
author_facet | Yamamizu, Kohei Sharov, Alexei A. Piao, Yulan Amano, Misa Yu, Hong Nishiyama, Akira Dudekula, Dawood B. Schlessinger, David Ko, Minoru S. H. |
author_sort | Yamamizu, Kohei |
collection | PubMed |
description | Mouse embryonic stem cells (ESCs) can differentiate into a wide range – and possibly all cell types in vitro, and thus provide an ideal platform to study systematically the action of transcription factors (TFs) in cell differentiation. Previously, we have generated and analyzed 137 TF-inducible mouse ESC lines. As an extension of this “NIA Mouse ESC Bank,” we generated and characterized 48 additional mouse ESC lines, in which single TFs in each line could be induced in a doxycycline-controllable manner. Together, with the previous ESC lines, the bank now comprises 185 TF-manipulable ESC lines (>10% of all mouse TFs). Global gene expression (transcriptome) profiling revealed that the induction of individual TFs in mouse ESCs for 48 hours shifts their transcriptomes toward specific differentiation fates (e.g., neural lineages by Myt1 Isl1, and St18; mesodermal lineages by Pitx1, Pitx2, Barhl2, and Lmx1a; white blood cells by Myb, Etv2, and Tbx6, and ovary by Pitx1, Pitx2, and Dmrtc2). These data also provide and lists of inferred target genes of each TF and possible functions of these TFs. The results demonstrate the utility of mouse ESC lines and their transcriptome data for understanding the mechanism of cell differentiation and the function of TFs. |
format | Online Article Text |
id | pubmed-4858678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48586782016-05-19 Generation and gene expression profiling of 48 transcription-factor-inducible mouse embryonic stem cell lines Yamamizu, Kohei Sharov, Alexei A. Piao, Yulan Amano, Misa Yu, Hong Nishiyama, Akira Dudekula, Dawood B. Schlessinger, David Ko, Minoru S. H. Sci Rep Article Mouse embryonic stem cells (ESCs) can differentiate into a wide range – and possibly all cell types in vitro, and thus provide an ideal platform to study systematically the action of transcription factors (TFs) in cell differentiation. Previously, we have generated and analyzed 137 TF-inducible mouse ESC lines. As an extension of this “NIA Mouse ESC Bank,” we generated and characterized 48 additional mouse ESC lines, in which single TFs in each line could be induced in a doxycycline-controllable manner. Together, with the previous ESC lines, the bank now comprises 185 TF-manipulable ESC lines (>10% of all mouse TFs). Global gene expression (transcriptome) profiling revealed that the induction of individual TFs in mouse ESCs for 48 hours shifts their transcriptomes toward specific differentiation fates (e.g., neural lineages by Myt1 Isl1, and St18; mesodermal lineages by Pitx1, Pitx2, Barhl2, and Lmx1a; white blood cells by Myb, Etv2, and Tbx6, and ovary by Pitx1, Pitx2, and Dmrtc2). These data also provide and lists of inferred target genes of each TF and possible functions of these TFs. The results demonstrate the utility of mouse ESC lines and their transcriptome data for understanding the mechanism of cell differentiation and the function of TFs. Nature Publishing Group 2016-05-06 /pmc/articles/PMC4858678/ /pubmed/27150017 http://dx.doi.org/10.1038/srep25667 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yamamizu, Kohei Sharov, Alexei A. Piao, Yulan Amano, Misa Yu, Hong Nishiyama, Akira Dudekula, Dawood B. Schlessinger, David Ko, Minoru S. H. Generation and gene expression profiling of 48 transcription-factor-inducible mouse embryonic stem cell lines |
title | Generation and gene expression profiling of 48 transcription-factor-inducible mouse embryonic stem cell lines |
title_full | Generation and gene expression profiling of 48 transcription-factor-inducible mouse embryonic stem cell lines |
title_fullStr | Generation and gene expression profiling of 48 transcription-factor-inducible mouse embryonic stem cell lines |
title_full_unstemmed | Generation and gene expression profiling of 48 transcription-factor-inducible mouse embryonic stem cell lines |
title_short | Generation and gene expression profiling of 48 transcription-factor-inducible mouse embryonic stem cell lines |
title_sort | generation and gene expression profiling of 48 transcription-factor-inducible mouse embryonic stem cell lines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858678/ https://www.ncbi.nlm.nih.gov/pubmed/27150017 http://dx.doi.org/10.1038/srep25667 |
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