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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Main Authors: Livia Vastag, Paul Jorgensen, Leonid Peshkin, Ru Wei, Joshua D Rabinowitz, Marc W Kirschner
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-02-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3035664?pdf=render
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spelling 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
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AT joshuadrabinowitz remodelingofthemetabolomeduringearlyfrogdevelopment
AT marcwkirschner remodelingofthemetabolomeduringearlyfrogdevelopment
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