Effects of seawater acidification on cell cycle control mechanisms in Strongylocentrotus purpuratus embryos.

Previous studies have shown fertilization and development of marine species can be significantly inhibited when the pH of sea water is artificially lowered. Little mechanistic understanding of these effects exists to date, but previous work has linked developmental inhibition to reduced cleavage rat...

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Main Authors: Sean P Place, Bryan W Smith
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3313954?pdf=render
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spelling doaj-d0f9fd8e070444f882f05f8f1bdf03fb2020-11-25T02:28:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3406810.1371/journal.pone.0034068Effects of seawater acidification on cell cycle control mechanisms in Strongylocentrotus purpuratus embryos.Sean P PlaceBryan W SmithPrevious studies have shown fertilization and development of marine species can be significantly inhibited when the pH of sea water is artificially lowered. Little mechanistic understanding of these effects exists to date, but previous work has linked developmental inhibition to reduced cleavage rates in embryos. To explore this further, we tested whether common cell cycle checkpoints were involved using three cellular biomarkers of cell cycle progression: (1) the onset of DNA synthesis, (2) production of a mitotic regulator, cyclin B, and (3) formation of the mitotic spindle. We grew embryos of the purple sea urchin, Strongylocentrotus purpuratus, in seawater artifically buffered to a pH of ∼7.0, 7.5, and 8.0 by CO(2) infusion. Our results suggest the reduced rates of mitotic cleavage are likely unrelated to common cell cycle checkpoints. We found no significant differences in the three biomarkers assessed between pH treatments, indicating the embryos progress through the G(1)/S, G(2)/M and metaphase/anaphase transitions at relatively similar rates. These data suggest low pH environments may not impact developmental programs directly, but may act through secondary mechanisms such as cellular energetics.http://europepmc.org/articles/PMC3313954?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sean P Place
Bryan W Smith
spellingShingle Sean P Place
Bryan W Smith
Effects of seawater acidification on cell cycle control mechanisms in Strongylocentrotus purpuratus embryos.
PLoS ONE
author_facet Sean P Place
Bryan W Smith
author_sort Sean P Place
title Effects of seawater acidification on cell cycle control mechanisms in Strongylocentrotus purpuratus embryos.
title_short Effects of seawater acidification on cell cycle control mechanisms in Strongylocentrotus purpuratus embryos.
title_full Effects of seawater acidification on cell cycle control mechanisms in Strongylocentrotus purpuratus embryos.
title_fullStr Effects of seawater acidification on cell cycle control mechanisms in Strongylocentrotus purpuratus embryos.
title_full_unstemmed Effects of seawater acidification on cell cycle control mechanisms in Strongylocentrotus purpuratus embryos.
title_sort effects of seawater acidification on cell cycle control mechanisms in strongylocentrotus purpuratus embryos.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Previous studies have shown fertilization and development of marine species can be significantly inhibited when the pH of sea water is artificially lowered. Little mechanistic understanding of these effects exists to date, but previous work has linked developmental inhibition to reduced cleavage rates in embryos. To explore this further, we tested whether common cell cycle checkpoints were involved using three cellular biomarkers of cell cycle progression: (1) the onset of DNA synthesis, (2) production of a mitotic regulator, cyclin B, and (3) formation of the mitotic spindle. We grew embryos of the purple sea urchin, Strongylocentrotus purpuratus, in seawater artifically buffered to a pH of ∼7.0, 7.5, and 8.0 by CO(2) infusion. Our results suggest the reduced rates of mitotic cleavage are likely unrelated to common cell cycle checkpoints. We found no significant differences in the three biomarkers assessed between pH treatments, indicating the embryos progress through the G(1)/S, G(2)/M and metaphase/anaphase transitions at relatively similar rates. These data suggest low pH environments may not impact developmental programs directly, but may act through secondary mechanisms such as cellular energetics.
url http://europepmc.org/articles/PMC3313954?pdf=render
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