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High‐throughput screening in postimplantation haploid epiblast stem cells reveals Hs3st3b1 as a modulator for reprogramming
Epiblast stem cells (EpiSCs) derived from postimplantation epiblast are pluripotent stem cells, epigenetically distinct from embryonic stem cells (ESCs), which are widely used in reprogramming studies. Recent achieved haploid cell lines in mammalian species open a new era for high‐throughput genetic...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046116/ https://www.ncbi.nlm.nih.gov/pubmed/33511777 http://dx.doi.org/10.1002/sctm.20-0468 |
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author | Gao, Qian Zhang, Wenhao Zhao, Yiding Tian, Yaru Wang, Yuna Zhang, Jinxin Geng, Mengyang Xu, Mei Yao, Chunmeng Wang, Haoyu Li, Luyuan Liu, Yan Shuai, Ling |
author_facet | Gao, Qian Zhang, Wenhao Zhao, Yiding Tian, Yaru Wang, Yuna Zhang, Jinxin Geng, Mengyang Xu, Mei Yao, Chunmeng Wang, Haoyu Li, Luyuan Liu, Yan Shuai, Ling |
author_sort | Gao, Qian |
collection | PubMed |
description | Epiblast stem cells (EpiSCs) derived from postimplantation epiblast are pluripotent stem cells, epigenetically distinct from embryonic stem cells (ESCs), which are widely used in reprogramming studies. Recent achieved haploid cell lines in mammalian species open a new era for high‐throughput genetic screening, due to their homozygous phenotypes. Here, we report the generation of mouse haploid EpiSCs (haEpiSCs) from postimplantation chimeric embryos at embryonic day 6.5 (E6.5). These cells maintain one set of chromosomes, express EpiSC‐specific genes, and have potentials to differentiate into three germ layers. We also develop a massive mutagenesis protocol with haEpiSCs, and subsequently perform reprogramming selection using this genome‐wide mutation library. Multiple modules related to various pathways are implicated. The validation experiments prove that knockout of Hst3st3b1 (one of the candidates) can promote reprogramming of EpiSCs to the ground state efficiently. Our results open the feasibility of utilizing haEpiSCs to elucidate fundamental biological processes including cell fate alternations. |
format | Online Article Text |
id | pubmed-8046116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80461162021-04-16 High‐throughput screening in postimplantation haploid epiblast stem cells reveals Hs3st3b1 as a modulator for reprogramming Gao, Qian Zhang, Wenhao Zhao, Yiding Tian, Yaru Wang, Yuna Zhang, Jinxin Geng, Mengyang Xu, Mei Yao, Chunmeng Wang, Haoyu Li, Luyuan Liu, Yan Shuai, Ling Stem Cells Transl Med Pluripotent Stem Cells Epiblast stem cells (EpiSCs) derived from postimplantation epiblast are pluripotent stem cells, epigenetically distinct from embryonic stem cells (ESCs), which are widely used in reprogramming studies. Recent achieved haploid cell lines in mammalian species open a new era for high‐throughput genetic screening, due to their homozygous phenotypes. Here, we report the generation of mouse haploid EpiSCs (haEpiSCs) from postimplantation chimeric embryos at embryonic day 6.5 (E6.5). These cells maintain one set of chromosomes, express EpiSC‐specific genes, and have potentials to differentiate into three germ layers. We also develop a massive mutagenesis protocol with haEpiSCs, and subsequently perform reprogramming selection using this genome‐wide mutation library. Multiple modules related to various pathways are implicated. The validation experiments prove that knockout of Hst3st3b1 (one of the candidates) can promote reprogramming of EpiSCs to the ground state efficiently. Our results open the feasibility of utilizing haEpiSCs to elucidate fundamental biological processes including cell fate alternations. John Wiley & Sons, Inc. 2021-01-29 /pmc/articles/PMC8046116/ /pubmed/33511777 http://dx.doi.org/10.1002/sctm.20-0468 Text en © 2021 The Authors. stem cells translational medicine published by Wiley Periodicals LLC on behalf of AlphaMed Press https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, 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 | Pluripotent Stem Cells Gao, Qian Zhang, Wenhao Zhao, Yiding Tian, Yaru Wang, Yuna Zhang, Jinxin Geng, Mengyang Xu, Mei Yao, Chunmeng Wang, Haoyu Li, Luyuan Liu, Yan Shuai, Ling High‐throughput screening in postimplantation haploid epiblast stem cells reveals Hs3st3b1 as a modulator for reprogramming |
title | High‐throughput screening in postimplantation haploid epiblast stem cells reveals Hs3st3b1 as a modulator for reprogramming |
title_full | High‐throughput screening in postimplantation haploid epiblast stem cells reveals Hs3st3b1 as a modulator for reprogramming |
title_fullStr | High‐throughput screening in postimplantation haploid epiblast stem cells reveals Hs3st3b1 as a modulator for reprogramming |
title_full_unstemmed | High‐throughput screening in postimplantation haploid epiblast stem cells reveals Hs3st3b1 as a modulator for reprogramming |
title_short | High‐throughput screening in postimplantation haploid epiblast stem cells reveals Hs3st3b1 as a modulator for reprogramming |
title_sort | high‐throughput screening in postimplantation haploid epiblast stem cells reveals hs3st3b1 as a modulator for reprogramming |
topic | Pluripotent Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046116/ https://www.ncbi.nlm.nih.gov/pubmed/33511777 http://dx.doi.org/10.1002/sctm.20-0468 |
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