Author
Listed:
- Claudia Gerri
(The Francis Crick Institute)
- Afshan McCarthy
(The Francis Crick Institute)
- Gregorio Alanis-Lobato
(The Francis Crick Institute)
- Andrej Demtschenko
(Vrije Universiteit Brussel)
- Alexandre Bruneau
(Université de Nantes, CHU Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN)
- Sophie Loubersac
(Université de Nantes, CHU Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN
Université de Nantes)
- Norah M. E. Fogarty
(The Francis Crick Institute
King’s College London)
- Daniel Hampshire
(Royal Veterinary College)
- Kay Elder
(Bourn Hall Clinic)
- Phil Snell
(Bourn Hall Clinic)
- Leila Christie
(Bourn Hall Clinic)
- Laurent David
(Université de Nantes, CHU Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN
Université de Nantes, CHU Nantes, Inserm, CNRS, SFR Santé, Inserm UMS 016, CNRS UMS 3556)
- Hilde Van de Velde
(Vrije Universiteit Brussel
Center for Reproductive Medicine, UZ-Brussel)
- Ali A. Fouladi-Nashta
(Royal Veterinary College)
- Kathy K. Niakan
(The Francis Crick Institute
University of Cambridge)
Abstract
Current understandings of cell specification in early mammalian pre-implantation development are based mainly on mouse studies. The first lineage differentiation event occurs at the morula stage, with outer cells initiating a trophectoderm (TE) placental progenitor program. The inner cell mass arises from inner cells during subsequent developmental stages and comprises precursor cells of the embryo proper and yolk sac1. Recent gene-expression analyses suggest that the mechanisms that regulate early lineage specification in the mouse may differ in other mammals, including human2–5 and cow6. Here we show the evolutionary conservation of a molecular cascade that initiates TE segregation in human, cow and mouse embryos. At the morula stage, outer cells acquire an apical–basal cell polarity, with expression of atypical protein kinase C (aPKC) at the contact-free domain, nuclear expression of Hippo signalling pathway effectors and restricted expression of TE-associated factors such as GATA3, which suggests initiation of a TE program. Furthermore, we demonstrate that inhibition of aPKC by small-molecule pharmacological modulation or Trim-Away protein depletion impairs TE initiation at the morula stage. Our comparative embryology analysis provides insights into early lineage specification and suggests that a similar mechanism initiates a TE program in human, cow and mouse embryos.
Suggested Citation
Claudia Gerri & Afshan McCarthy & Gregorio Alanis-Lobato & Andrej Demtschenko & Alexandre Bruneau & Sophie Loubersac & Norah M. E. Fogarty & Daniel Hampshire & Kay Elder & Phil Snell & Leila Christie , 2020.
"Initiation of a conserved trophectoderm program in human, cow and mouse embryos,"
Nature, Nature, vol. 587(7834), pages 443-447, November.
Handle:
RePEc:nat:nature:v:587:y:2020:i:7834:d:10.1038_s41586-020-2759-x
DOI: 10.1038/s41586-020-2759-x
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Cited by:
- Chen Dong & Shuhua Fu & Rowan M. Karvas & Brian Chew & Laura A. Fischer & Xiaoyun Xing & Jessica K. Harrison & Pooja Popli & Ramakrishna Kommagani & Ting Wang & Bo Zhang & Thorold W. Theunissen, 2022.
"A genome-wide CRISPR-Cas9 knockout screen identifies essential and growth-restricting genes in human trophoblast stem cells,"
Nature Communications, Nature, vol. 13(1), pages 1-16, December.
- Nicolas Allègre & Sabine Chauveau & Cynthia Dennis & Yoan Renaud & Dimitri Meistermann & Lorena Valverde Estrella & Pierre Pouchin & Michel Cohen-Tannoudji & Laurent David & Claire Chazaud, 2022.
"NANOG initiates epiblast fate through the coordination of pluripotency genes expression,"
Nature Communications, Nature, vol. 13(1), pages 1-13, December.
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