Cargando…
A hexa-species transcriptome atlas of mammalian embryogenesis delineates metabolic regulation across three different implantation modes
Mammalian embryogenesis relies on glycolysis and oxidative phosphorylation to balance the generation of biomass with energy production. However, the dynamics of metabolic regulation in the postimplantation embryo in vivo have remained elusive due to the inaccessibility of the implanted conceptus for...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203550/ https://www.ncbi.nlm.nih.gov/pubmed/35710749 http://dx.doi.org/10.1038/s41467-022-30194-x |
_version_ | 1784728730054164480 |
---|---|
author | Malkowska, Anna Penfold, Christopher Bergmann, Sophie Boroviak, Thorsten E. |
author_facet | Malkowska, Anna Penfold, Christopher Bergmann, Sophie Boroviak, Thorsten E. |
author_sort | Malkowska, Anna |
collection | PubMed |
description | Mammalian embryogenesis relies on glycolysis and oxidative phosphorylation to balance the generation of biomass with energy production. However, the dynamics of metabolic regulation in the postimplantation embryo in vivo have remained elusive due to the inaccessibility of the implanted conceptus for biochemical studies. To address this issue, we compiled single-cell embryo profiling data in six mammalian species and determined their metabolic dynamics through glycolysis and oxidative phosphorylation associated gene expression. Strikingly, we identify a conserved switch from bivalent respiration in the late blastocyst towards a glycolytic metabolism in early gastrulation stages across species, which is independent of embryo implantation. Extraembryonic lineages followed the dynamics of the embryonic lineage, except visceral endoderm. Finally, we demonstrate that in vitro primate embryo culture substantially impacts metabolic gene regulation by comparison to in vivo samples. Our work reveals a conserved metabolic programme despite different implantation modes and highlights the need to optimise postimplantation embryo culture protocols. |
format | Online Article Text |
id | pubmed-9203550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92035502022-06-18 A hexa-species transcriptome atlas of mammalian embryogenesis delineates metabolic regulation across three different implantation modes Malkowska, Anna Penfold, Christopher Bergmann, Sophie Boroviak, Thorsten E. Nat Commun Article Mammalian embryogenesis relies on glycolysis and oxidative phosphorylation to balance the generation of biomass with energy production. However, the dynamics of metabolic regulation in the postimplantation embryo in vivo have remained elusive due to the inaccessibility of the implanted conceptus for biochemical studies. To address this issue, we compiled single-cell embryo profiling data in six mammalian species and determined their metabolic dynamics through glycolysis and oxidative phosphorylation associated gene expression. Strikingly, we identify a conserved switch from bivalent respiration in the late blastocyst towards a glycolytic metabolism in early gastrulation stages across species, which is independent of embryo implantation. Extraembryonic lineages followed the dynamics of the embryonic lineage, except visceral endoderm. Finally, we demonstrate that in vitro primate embryo culture substantially impacts metabolic gene regulation by comparison to in vivo samples. Our work reveals a conserved metabolic programme despite different implantation modes and highlights the need to optimise postimplantation embryo culture protocols. Nature Publishing Group UK 2022-06-16 /pmc/articles/PMC9203550/ /pubmed/35710749 http://dx.doi.org/10.1038/s41467-022-30194-x Text en © The Author(s) 2022 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 Malkowska, Anna Penfold, Christopher Bergmann, Sophie Boroviak, Thorsten E. A hexa-species transcriptome atlas of mammalian embryogenesis delineates metabolic regulation across three different implantation modes |
title | A hexa-species transcriptome atlas of mammalian embryogenesis delineates metabolic regulation across three different implantation modes |
title_full | A hexa-species transcriptome atlas of mammalian embryogenesis delineates metabolic regulation across three different implantation modes |
title_fullStr | A hexa-species transcriptome atlas of mammalian embryogenesis delineates metabolic regulation across three different implantation modes |
title_full_unstemmed | A hexa-species transcriptome atlas of mammalian embryogenesis delineates metabolic regulation across three different implantation modes |
title_short | A hexa-species transcriptome atlas of mammalian embryogenesis delineates metabolic regulation across three different implantation modes |
title_sort | hexa-species transcriptome atlas of mammalian embryogenesis delineates metabolic regulation across three different implantation modes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203550/ https://www.ncbi.nlm.nih.gov/pubmed/35710749 http://dx.doi.org/10.1038/s41467-022-30194-x |
work_keys_str_mv | AT malkowskaanna ahexaspeciestranscriptomeatlasofmammalianembryogenesisdelineatesmetabolicregulationacrossthreedifferentimplantationmodes AT penfoldchristopher ahexaspeciestranscriptomeatlasofmammalianembryogenesisdelineatesmetabolicregulationacrossthreedifferentimplantationmodes AT bergmannsophie ahexaspeciestranscriptomeatlasofmammalianembryogenesisdelineatesmetabolicregulationacrossthreedifferentimplantationmodes AT boroviakthorstene ahexaspeciestranscriptomeatlasofmammalianembryogenesisdelineatesmetabolicregulationacrossthreedifferentimplantationmodes AT malkowskaanna hexaspeciestranscriptomeatlasofmammalianembryogenesisdelineatesmetabolicregulationacrossthreedifferentimplantationmodes AT penfoldchristopher hexaspeciestranscriptomeatlasofmammalianembryogenesisdelineatesmetabolicregulationacrossthreedifferentimplantationmodes AT bergmannsophie hexaspeciestranscriptomeatlasofmammalianembryogenesisdelineatesmetabolicregulationacrossthreedifferentimplantationmodes AT boroviakthorstene hexaspeciestranscriptomeatlasofmammalianembryogenesisdelineatesmetabolicregulationacrossthreedifferentimplantationmodes |