Cargo transport by cytoplasmic Dynein can center embryonic centrosomes.

To complete meiosis II in animal cells, the male DNA material needs to meet the female DNA material contained in the female pronucleus at the egg center, but it is not known how the male pronucleus, deposited by the sperm at the periphery of the cell, finds the cell center in large eggs. Pronucleus...

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Main Authors: Rafael A Longoria, George T Shubeita
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3698173?pdf=render
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spelling doaj-505aef3cb17643f5b58da2ca3e8251d82020-11-25T01:20:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e6771010.1371/journal.pone.0067710Cargo transport by cytoplasmic Dynein can center embryonic centrosomes.Rafael A LongoriaGeorge T ShubeitaTo complete meiosis II in animal cells, the male DNA material needs to meet the female DNA material contained in the female pronucleus at the egg center, but it is not known how the male pronucleus, deposited by the sperm at the periphery of the cell, finds the cell center in large eggs. Pronucleus centering is an active process that appears to involve microtubules and molecular motors. For small and medium-sized cells, the force required to move the centrosome can arise from either microtubule pushing on the cortex, or cortically-attached dynein pulling on microtubules. However, in large cells, such as the fertilized Xenopus laevis embryo, where microtubules are too long to support pushing forces or they do not reach all boundaries before centrosome centering begins, a different force generating mechanism must exist. Here, we present a centrosome positioning model in which the cytosolic drag experienced by cargoes hauled by cytoplasmic dynein on the sperm aster microtubules can move the centrosome towards the cell's center. We find that small, fast cargoes (diameter ∼100 nm, cargo velocity ∼2 µm/s) are sufficient to move the centrosome in the geometry of the Xenopus laevis embryo within the experimentally observed length and time scales.http://europepmc.org/articles/PMC3698173?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rafael A Longoria
George T Shubeita
spellingShingle Rafael A Longoria
George T Shubeita
Cargo transport by cytoplasmic Dynein can center embryonic centrosomes.
PLoS ONE
author_facet Rafael A Longoria
George T Shubeita
author_sort Rafael A Longoria
title Cargo transport by cytoplasmic Dynein can center embryonic centrosomes.
title_short Cargo transport by cytoplasmic Dynein can center embryonic centrosomes.
title_full Cargo transport by cytoplasmic Dynein can center embryonic centrosomes.
title_fullStr Cargo transport by cytoplasmic Dynein can center embryonic centrosomes.
title_full_unstemmed Cargo transport by cytoplasmic Dynein can center embryonic centrosomes.
title_sort cargo transport by cytoplasmic dynein can center embryonic centrosomes.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description To complete meiosis II in animal cells, the male DNA material needs to meet the female DNA material contained in the female pronucleus at the egg center, but it is not known how the male pronucleus, deposited by the sperm at the periphery of the cell, finds the cell center in large eggs. Pronucleus centering is an active process that appears to involve microtubules and molecular motors. For small and medium-sized cells, the force required to move the centrosome can arise from either microtubule pushing on the cortex, or cortically-attached dynein pulling on microtubules. However, in large cells, such as the fertilized Xenopus laevis embryo, where microtubules are too long to support pushing forces or they do not reach all boundaries before centrosome centering begins, a different force generating mechanism must exist. Here, we present a centrosome positioning model in which the cytosolic drag experienced by cargoes hauled by cytoplasmic dynein on the sperm aster microtubules can move the centrosome towards the cell's center. We find that small, fast cargoes (diameter ∼100 nm, cargo velocity ∼2 µm/s) are sufficient to move the centrosome in the geometry of the Xenopus laevis embryo within the experimentally observed length and time scales.
url http://europepmc.org/articles/PMC3698173?pdf=render
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AT georgetshubeita cargotransportbycytoplasmicdyneincancenterembryoniccentrosomes
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