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PLK-1 Regulation of Asymmetric Cell Division in the Early C. elegans Embryo

PLK1 is a conserved mitotic kinase that is essential for the entry into and progression through mitosis. In addition to its canonical mitotic functions, recent studies have characterized a critical role for PLK-1 in regulating the polarization and asymmetric division of the one-cell C. elegans embry...

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Autores principales: Kim, Amelia J., Griffin, Erik E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859328/
https://www.ncbi.nlm.nih.gov/pubmed/33553173
http://dx.doi.org/10.3389/fcell.2020.632253
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author Kim, Amelia J.
Griffin, Erik E.
author_facet Kim, Amelia J.
Griffin, Erik E.
author_sort Kim, Amelia J.
collection PubMed
description PLK1 is a conserved mitotic kinase that is essential for the entry into and progression through mitosis. In addition to its canonical mitotic functions, recent studies have characterized a critical role for PLK-1 in regulating the polarization and asymmetric division of the one-cell C. elegans embryo. Prior to cell division, PLK-1 regulates both the polarization of the PAR proteins at the cell cortex and the segregation of cell fate determinants in the cytoplasm. Following cell division, PLK-1 is preferentially inherited to one daughter cell where it acts to regulate the timing of centrosome separation and cell division. PLK1 also regulates cell polarity in asymmetrically dividing Drosophila neuroblasts and during mammalian planar cell polarity, suggesting it may act broadly to connect cell polarity and cell cycle mechanisms.
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spelling pubmed-78593282021-02-05 PLK-1 Regulation of Asymmetric Cell Division in the Early C. elegans Embryo Kim, Amelia J. Griffin, Erik E. Front Cell Dev Biol Cell and Developmental Biology PLK1 is a conserved mitotic kinase that is essential for the entry into and progression through mitosis. In addition to its canonical mitotic functions, recent studies have characterized a critical role for PLK-1 in regulating the polarization and asymmetric division of the one-cell C. elegans embryo. Prior to cell division, PLK-1 regulates both the polarization of the PAR proteins at the cell cortex and the segregation of cell fate determinants in the cytoplasm. Following cell division, PLK-1 is preferentially inherited to one daughter cell where it acts to regulate the timing of centrosome separation and cell division. PLK1 also regulates cell polarity in asymmetrically dividing Drosophila neuroblasts and during mammalian planar cell polarity, suggesting it may act broadly to connect cell polarity and cell cycle mechanisms. Frontiers Media S.A. 2021-01-21 /pmc/articles/PMC7859328/ /pubmed/33553173 http://dx.doi.org/10.3389/fcell.2020.632253 Text en Copyright © 2021 Kim and Griffin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Kim, Amelia J.
Griffin, Erik E.
PLK-1 Regulation of Asymmetric Cell Division in the Early C. elegans Embryo
title PLK-1 Regulation of Asymmetric Cell Division in the Early C. elegans Embryo
title_full PLK-1 Regulation of Asymmetric Cell Division in the Early C. elegans Embryo
title_fullStr PLK-1 Regulation of Asymmetric Cell Division in the Early C. elegans Embryo
title_full_unstemmed PLK-1 Regulation of Asymmetric Cell Division in the Early C. elegans Embryo
title_short PLK-1 Regulation of Asymmetric Cell Division in the Early C. elegans Embryo
title_sort plk-1 regulation of asymmetric cell division in the early c. elegans embryo
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859328/
https://www.ncbi.nlm.nih.gov/pubmed/33553173
http://dx.doi.org/10.3389/fcell.2020.632253
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