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Amnion signals are essential for mesoderm formation in primates

Embryonic development is largely conserved among mammals. However, certain genes show divergent functions. By generating a transcriptional atlas containing >30,000 cells from post-implantation non-human primate embryos, we uncover that ISL1, a gene with a well-established role in cardiogenesis, c...

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Autores principales: Yang, Ran, Goedel, Alexander, Kang, Yu, Si, Chenyang, Chu, Chu, Zheng, Yi, Chen, Zhenzhen, Gruber, Peter J., Xiao, Yao, Zhou, Chikai, Witman, Nevin, Eroglu, Elif, Leung, Chuen-Yan, Chen, Yongchang, Fu, Jianping, Ji, Weizhi, Lanner, Fredrik, Niu, Yuyu, Chien, Kenneth R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390679/
https://www.ncbi.nlm.nih.gov/pubmed/34446705
http://dx.doi.org/10.1038/s41467-021-25186-2
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author Yang, Ran
Goedel, Alexander
Kang, Yu
Si, Chenyang
Chu, Chu
Zheng, Yi
Chen, Zhenzhen
Gruber, Peter J.
Xiao, Yao
Zhou, Chikai
Witman, Nevin
Eroglu, Elif
Leung, Chuen-Yan
Chen, Yongchang
Fu, Jianping
Ji, Weizhi
Lanner, Fredrik
Niu, Yuyu
Chien, Kenneth R.
author_facet Yang, Ran
Goedel, Alexander
Kang, Yu
Si, Chenyang
Chu, Chu
Zheng, Yi
Chen, Zhenzhen
Gruber, Peter J.
Xiao, Yao
Zhou, Chikai
Witman, Nevin
Eroglu, Elif
Leung, Chuen-Yan
Chen, Yongchang
Fu, Jianping
Ji, Weizhi
Lanner, Fredrik
Niu, Yuyu
Chien, Kenneth R.
author_sort Yang, Ran
collection PubMed
description Embryonic development is largely conserved among mammals. However, certain genes show divergent functions. By generating a transcriptional atlas containing >30,000 cells from post-implantation non-human primate embryos, we uncover that ISL1, a gene with a well-established role in cardiogenesis, controls a gene regulatory network in primate amnion. CRISPR/Cas9-targeting of ISL1 results in non-human primate embryos which do not yield viable offspring, demonstrating that ISL1 is critically required in primate embryogenesis. On a cellular level, mutant ISL1 embryos display a failure in mesoderm formation due to reduced BMP4 signaling from the amnion. Via loss of function and rescue studies in human embryonic stem cells we confirm a similar role of ISL1 in human in vitro derived amnion. This study highlights the importance of the amnion as a signaling center during primate mesoderm formation and demonstrates the potential of in vitro primate model systems to dissect the genetics of early human embryonic development.
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spelling pubmed-83906792021-09-22 Amnion signals are essential for mesoderm formation in primates Yang, Ran Goedel, Alexander Kang, Yu Si, Chenyang Chu, Chu Zheng, Yi Chen, Zhenzhen Gruber, Peter J. Xiao, Yao Zhou, Chikai Witman, Nevin Eroglu, Elif Leung, Chuen-Yan Chen, Yongchang Fu, Jianping Ji, Weizhi Lanner, Fredrik Niu, Yuyu Chien, Kenneth R. Nat Commun Article Embryonic development is largely conserved among mammals. However, certain genes show divergent functions. By generating a transcriptional atlas containing >30,000 cells from post-implantation non-human primate embryos, we uncover that ISL1, a gene with a well-established role in cardiogenesis, controls a gene regulatory network in primate amnion. CRISPR/Cas9-targeting of ISL1 results in non-human primate embryos which do not yield viable offspring, demonstrating that ISL1 is critically required in primate embryogenesis. On a cellular level, mutant ISL1 embryos display a failure in mesoderm formation due to reduced BMP4 signaling from the amnion. Via loss of function and rescue studies in human embryonic stem cells we confirm a similar role of ISL1 in human in vitro derived amnion. This study highlights the importance of the amnion as a signaling center during primate mesoderm formation and demonstrates the potential of in vitro primate model systems to dissect the genetics of early human embryonic development. Nature Publishing Group UK 2021-08-26 /pmc/articles/PMC8390679/ /pubmed/34446705 http://dx.doi.org/10.1038/s41467-021-25186-2 Text en © The Author(s) 2021 https://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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yang, Ran
Goedel, Alexander
Kang, Yu
Si, Chenyang
Chu, Chu
Zheng, Yi
Chen, Zhenzhen
Gruber, Peter J.
Xiao, Yao
Zhou, Chikai
Witman, Nevin
Eroglu, Elif
Leung, Chuen-Yan
Chen, Yongchang
Fu, Jianping
Ji, Weizhi
Lanner, Fredrik
Niu, Yuyu
Chien, Kenneth R.
Amnion signals are essential for mesoderm formation in primates
title Amnion signals are essential for mesoderm formation in primates
title_full Amnion signals are essential for mesoderm formation in primates
title_fullStr Amnion signals are essential for mesoderm formation in primates
title_full_unstemmed Amnion signals are essential for mesoderm formation in primates
title_short Amnion signals are essential for mesoderm formation in primates
title_sort amnion signals are essential for mesoderm formation in primates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390679/
https://www.ncbi.nlm.nih.gov/pubmed/34446705
http://dx.doi.org/10.1038/s41467-021-25186-2
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