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...
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doaj-870c35c4740f42b6ad528ef5451fa2672020-11-25T00:23:38ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-02-0162e1688110.1371/journal.pone.0016881Remodeling of the metabolome during early frog development.Livia VastagPaul JorgensenLeonid PeshkinRu WeiJoshua D RabinowitzMarc W KirschnerA 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.http://europepmc.org/articles/PMC3035664?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Livia Vastag Paul Jorgensen Leonid Peshkin Ru Wei Joshua D Rabinowitz Marc W Kirschner |
spellingShingle |
Livia Vastag Paul Jorgensen Leonid Peshkin Ru Wei Joshua D Rabinowitz Marc W Kirschner Remodeling of the metabolome during early frog development. PLoS ONE |
author_facet |
Livia Vastag Paul Jorgensen Leonid Peshkin Ru Wei Joshua D Rabinowitz Marc W Kirschner |
author_sort |
Livia Vastag |
title |
Remodeling of the metabolome during early frog development. |
title_short |
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_sort |
remodeling of the metabolome during early frog development. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2011-02-01 |
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. |
url |
http://europepmc.org/articles/PMC3035664?pdf=render |
work_keys_str_mv |
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