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Principles of early human development and germ cell program from conserved model systems

Human primordial germ cells (hPGCs), the precursors of sperm and eggs, originate during week 2-3 of early postimplantation development1. Using in vitro models of hPGC induction2–4, recent studies suggest striking mechanistic differences in specification of human and mouse PGCs5. This may partly be d...

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Autores principales: Kobayashi, Toshihiro, Zhang, Haixin, Tang, Walfred W.C., Irie, Naoko, Withey, Sarah, Klisch, Doris, Sybirna, Anastasiya, Dietmann, Sabine, Contreras, David A., Webb, Robert, Allegrucci, Cinzia, Alberio, Ramiro, Surani, M. Azim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473469/
https://www.ncbi.nlm.nih.gov/pubmed/28607482
http://dx.doi.org/10.1038/nature22812
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author Kobayashi, Toshihiro
Zhang, Haixin
Tang, Walfred W.C.
Irie, Naoko
Withey, Sarah
Klisch, Doris
Sybirna, Anastasiya
Dietmann, Sabine
Contreras, David A.
Webb, Robert
Allegrucci, Cinzia
Alberio, Ramiro
Surani, M. Azim
author_facet Kobayashi, Toshihiro
Zhang, Haixin
Tang, Walfred W.C.
Irie, Naoko
Withey, Sarah
Klisch, Doris
Sybirna, Anastasiya
Dietmann, Sabine
Contreras, David A.
Webb, Robert
Allegrucci, Cinzia
Alberio, Ramiro
Surani, M. Azim
author_sort Kobayashi, Toshihiro
collection PubMed
description Human primordial germ cells (hPGCs), the precursors of sperm and eggs, originate during week 2-3 of early postimplantation development1. Using in vitro models of hPGC induction2–4, recent studies suggest striking mechanistic differences in specification of human and mouse PGCs5. This may partly be due to the divergence in their pluripotency networks, and early postimplantation development6–8. Since early human embryos are inaccessible for direct studies, we considered alternatives, including porcine embryos that, as in humans, develop as bilaminar embryonic discs. Here we show that porcine PGCs (pPGCs) originate from the posterior pre-primitive streak competent epiblast by sequential upregulation of SOX17 and BLIMP1 in response to WNT and BMP signalling. Together with human and monkey in vitro models simulating peri-gastrulation development, we show conserved principles for epiblast development for competency for PGC fate, followed by initiation of the epigenetic programme9–11, regulated by a balanced SOX17–BLIMP1 gene dosage. Our combinatorial approach using human, porcine and monkey in vivo and in vitro models, provides synthetic insights on early human development.
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spelling pubmed-54734692017-12-07 Principles of early human development and germ cell program from conserved model systems Kobayashi, Toshihiro Zhang, Haixin Tang, Walfred W.C. Irie, Naoko Withey, Sarah Klisch, Doris Sybirna, Anastasiya Dietmann, Sabine Contreras, David A. Webb, Robert Allegrucci, Cinzia Alberio, Ramiro Surani, M. Azim Nature Article Human primordial germ cells (hPGCs), the precursors of sperm and eggs, originate during week 2-3 of early postimplantation development1. Using in vitro models of hPGC induction2–4, recent studies suggest striking mechanistic differences in specification of human and mouse PGCs5. This may partly be due to the divergence in their pluripotency networks, and early postimplantation development6–8. Since early human embryos are inaccessible for direct studies, we considered alternatives, including porcine embryos that, as in humans, develop as bilaminar embryonic discs. Here we show that porcine PGCs (pPGCs) originate from the posterior pre-primitive streak competent epiblast by sequential upregulation of SOX17 and BLIMP1 in response to WNT and BMP signalling. Together with human and monkey in vitro models simulating peri-gastrulation development, we show conserved principles for epiblast development for competency for PGC fate, followed by initiation of the epigenetic programme9–11, regulated by a balanced SOX17–BLIMP1 gene dosage. Our combinatorial approach using human, porcine and monkey in vivo and in vitro models, provides synthetic insights on early human development. 2017-06-07 2017-06-15 /pmc/articles/PMC5473469/ /pubmed/28607482 http://dx.doi.org/10.1038/nature22812 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kobayashi, Toshihiro
Zhang, Haixin
Tang, Walfred W.C.
Irie, Naoko
Withey, Sarah
Klisch, Doris
Sybirna, Anastasiya
Dietmann, Sabine
Contreras, David A.
Webb, Robert
Allegrucci, Cinzia
Alberio, Ramiro
Surani, M. Azim
Principles of early human development and germ cell program from conserved model systems
title Principles of early human development and germ cell program from conserved model systems
title_full Principles of early human development and germ cell program from conserved model systems
title_fullStr Principles of early human development and germ cell program from conserved model systems
title_full_unstemmed Principles of early human development and germ cell program from conserved model systems
title_short Principles of early human development and germ cell program from conserved model systems
title_sort principles of early human development and germ cell program from conserved model systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473469/
https://www.ncbi.nlm.nih.gov/pubmed/28607482
http://dx.doi.org/10.1038/nature22812
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