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Remodeling of the Metabolome during Early Frog Development
A rapid series of synchronous cell divisions initiates embryogenesis in many animal species, including the frog Xenopus laevis. After many of these cleavage cycles, the nuclear to cytoplasmic ratio increases sufficiently to somehow cause cell cycles to elongate and become asynchronous at the mid-bla...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035664/ https://www.ncbi.nlm.nih.gov/pubmed/21347444 http://dx.doi.org/10.1371/journal.pone.0016881 |
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author | Vastag, Livia Jorgensen, Paul Peshkin, Leonid Wei, Ru Rabinowitz, Joshua D. Kirschner, Marc W. |
author_facet | Vastag, Livia Jorgensen, Paul Peshkin, Leonid Wei, Ru Rabinowitz, Joshua D. Kirschner, Marc W. |
author_sort | Vastag, Livia |
collection | PubMed |
description | A rapid series of synchronous cell divisions initiates embryogenesis in many animal species, including the frog Xenopus laevis. After many of these cleavage cycles, the nuclear to cytoplasmic ratio increases sufficiently to somehow cause cell cycles to elongate and become asynchronous at the mid-blastula transition (MBT). We have discovered that an unanticipated remodeling of core metabolic pathways occurs during the cleavage cycles and the MBT in X.laevis, as evidenced by widespread changes in metabolite abundance. While many of the changes in metabolite abundance were consistently observed, it was also evident that different female frogs laid eggs with different levels of at least some metabolites. Metabolite tracing with heavy isotopes demonstrated that alanine is consumed to generate energy for the early embryo. dATP pools were found to decline during the MBT and we have confirmed that maternal pools of dNTPs are functionally exhausted at the onset of the MBT. Our results support an alternative hypothesis that the cell cycle lengthening at the MBT is triggered not by a limiting maternal protein, as is usually proposed, but by a decline in dNTP pools brought about by the exponentially increasing demands of DNA synthesis. |
format | Text |
id | pubmed-3035664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30356642011-02-23 Remodeling of the Metabolome during Early Frog Development Vastag, Livia Jorgensen, Paul Peshkin, Leonid Wei, Ru Rabinowitz, Joshua D. Kirschner, Marc W. PLoS One Research Article A rapid series of synchronous cell divisions initiates embryogenesis in many animal species, including the frog Xenopus laevis. After many of these cleavage cycles, the nuclear to cytoplasmic ratio increases sufficiently to somehow cause cell cycles to elongate and become asynchronous at the mid-blastula transition (MBT). We have discovered that an unanticipated remodeling of core metabolic pathways occurs during the cleavage cycles and the MBT in X.laevis, as evidenced by widespread changes in metabolite abundance. While many of the changes in metabolite abundance were consistently observed, it was also evident that different female frogs laid eggs with different levels of at least some metabolites. Metabolite tracing with heavy isotopes demonstrated that alanine is consumed to generate energy for the early embryo. dATP pools were found to decline during the MBT and we have confirmed that maternal pools of dNTPs are functionally exhausted at the onset of the MBT. Our results support an alternative hypothesis that the cell cycle lengthening at the MBT is triggered not by a limiting maternal protein, as is usually proposed, but by a decline in dNTP pools brought about by the exponentially increasing demands of DNA synthesis. Public Library of Science 2011-02-04 /pmc/articles/PMC3035664/ /pubmed/21347444 http://dx.doi.org/10.1371/journal.pone.0016881 Text en Vastag et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Vastag, Livia Jorgensen, Paul Peshkin, Leonid Wei, Ru Rabinowitz, Joshua D. Kirschner, Marc W. Remodeling of the Metabolome during Early Frog Development |
title | Remodeling of the Metabolome during Early Frog Development |
title_full | Remodeling of the Metabolome during Early Frog Development |
title_fullStr | Remodeling of the Metabolome during Early Frog Development |
title_full_unstemmed | Remodeling of the Metabolome during Early Frog Development |
title_short | Remodeling of the Metabolome during Early Frog Development |
title_sort | remodeling of the metabolome during early frog development |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035664/ https://www.ncbi.nlm.nih.gov/pubmed/21347444 http://dx.doi.org/10.1371/journal.pone.0016881 |
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