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Totipotency segregates between the sister blastomeres of two-cell stage mouse embryos
Following fertilization in mammals, it is generally accepted that totipotent cells are exclusive to the zygote and to each of the two blastomeres originating from the first mitotic division. This model of totipotency was inferred from a minority of cases in which blastomeres produced monozygotic twi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557898/ https://www.ncbi.nlm.nih.gov/pubmed/28811525 http://dx.doi.org/10.1038/s41598-017-08266-6 |
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author | Casser, E. Israel, S. Witten, A. Schulte, K. Schlatt, S. Nordhoff, V. Boiani, M. |
author_facet | Casser, E. Israel, S. Witten, A. Schulte, K. Schlatt, S. Nordhoff, V. Boiani, M. |
author_sort | Casser, E. |
collection | PubMed |
description | Following fertilization in mammals, it is generally accepted that totipotent cells are exclusive to the zygote and to each of the two blastomeres originating from the first mitotic division. This model of totipotency was inferred from a minority of cases in which blastomeres produced monozygotic twins in mice. Was this due to experimental limitation or biological constraint? Here we removed experimental obstacles and achieved reliable quantification of the prevalence of dual totipotency among mouse two-cell stage blastomeres. We separated the blastomeres of 1,252 two-cell embryos, preserving 1,210 of the pairs. Two classes of monozygotic twins became apparent at the blastocyst stage: 27% formed a functional epiblast in both members (concordant), and 73% did so in only one member of the pair (discordant) – a partition that proved insensitive to oocyte quality, sperm-entry point, culture environment and pattern of cleavage. In intact two-cell embryos, the ability of sister blastomeres to generate epiblast was also skewed. Class discovery clustering of the individual blastomeres’ and blastocysts’ transcriptomes points to an innate origin of concordance and discordance rather than developmental acquisition. Our data place constraints on the commonly accepted idea that totipotency is allocated equally between the two-cell stage blastomeres in mice. |
format | Online Article Text |
id | pubmed-5557898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55578982017-08-16 Totipotency segregates between the sister blastomeres of two-cell stage mouse embryos Casser, E. Israel, S. Witten, A. Schulte, K. Schlatt, S. Nordhoff, V. Boiani, M. Sci Rep Article Following fertilization in mammals, it is generally accepted that totipotent cells are exclusive to the zygote and to each of the two blastomeres originating from the first mitotic division. This model of totipotency was inferred from a minority of cases in which blastomeres produced monozygotic twins in mice. Was this due to experimental limitation or biological constraint? Here we removed experimental obstacles and achieved reliable quantification of the prevalence of dual totipotency among mouse two-cell stage blastomeres. We separated the blastomeres of 1,252 two-cell embryos, preserving 1,210 of the pairs. Two classes of monozygotic twins became apparent at the blastocyst stage: 27% formed a functional epiblast in both members (concordant), and 73% did so in only one member of the pair (discordant) – a partition that proved insensitive to oocyte quality, sperm-entry point, culture environment and pattern of cleavage. In intact two-cell embryos, the ability of sister blastomeres to generate epiblast was also skewed. Class discovery clustering of the individual blastomeres’ and blastocysts’ transcriptomes points to an innate origin of concordance and discordance rather than developmental acquisition. Our data place constraints on the commonly accepted idea that totipotency is allocated equally between the two-cell stage blastomeres in mice. Nature Publishing Group UK 2017-08-15 /pmc/articles/PMC5557898/ /pubmed/28811525 http://dx.doi.org/10.1038/s41598-017-08266-6 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Casser, E. Israel, S. Witten, A. Schulte, K. Schlatt, S. Nordhoff, V. Boiani, M. Totipotency segregates between the sister blastomeres of two-cell stage mouse embryos |
title | Totipotency segregates between the sister blastomeres of two-cell stage mouse embryos |
title_full | Totipotency segregates between the sister blastomeres of two-cell stage mouse embryos |
title_fullStr | Totipotency segregates between the sister blastomeres of two-cell stage mouse embryos |
title_full_unstemmed | Totipotency segregates between the sister blastomeres of two-cell stage mouse embryos |
title_short | Totipotency segregates between the sister blastomeres of two-cell stage mouse embryos |
title_sort | totipotency segregates between the sister blastomeres of two-cell stage mouse embryos |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557898/ https://www.ncbi.nlm.nih.gov/pubmed/28811525 http://dx.doi.org/10.1038/s41598-017-08266-6 |
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