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KIF20A Regulates Porcine Oocyte Maturation and Early Embryo Development
KIF20A (Kinesin-like family member 20A), also called mitotic kinesin-like proteins 2 (MKLP2), is a mammalian mitotic kinesin-like motor protein of the Kinesin superfamily proteins (KIFs), which was originally involved in Golgi apparatus dynamics and thought to essential for cell cycle regulation dur...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103861/ https://www.ncbi.nlm.nih.gov/pubmed/25036038 http://dx.doi.org/10.1371/journal.pone.0102898 |
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author | Zhang, Yu Liu, Jun Peng, Xu Zhu, Cheng-Cheng Han, Jun Luo, Jia Rui, Rong |
author_facet | Zhang, Yu Liu, Jun Peng, Xu Zhu, Cheng-Cheng Han, Jun Luo, Jia Rui, Rong |
author_sort | Zhang, Yu |
collection | PubMed |
description | KIF20A (Kinesin-like family member 20A), also called mitotic kinesin-like proteins 2 (MKLP2), is a mammalian mitotic kinesin-like motor protein of the Kinesin superfamily proteins (KIFs), which was originally involved in Golgi apparatus dynamics and thought to essential for cell cycle regulation during successful cytokinesis. In the present study, we investigated whether KIF20A has roles on porcine oocyte meiotic maturation and subsequent early embryo development. By immunofluorescence staining, KIF20A was found to exhibit a dynamic localization pattern during meiosis. KIF20A was restricted to centromeres after germinal vesicle breakdown (GVBD), transferred to the midbody at telophase I (TI), and again associated with centromeres at metaphase II (MII). Inhibition of endogenous KIF20A via a specific inhibitor, Paprotrain, resulted in failure of polar body extrusion. Further cell cycle analysis showed that the percentage of oocytes that arrested at early metaphase I (MI) stage increased after KIF20A activity inhibition; however, the proportion of oocytes at anaphase/telophase I (ATI) and MII stages decreased significantly. Our results also showed that KIF20A inhibition did not affect spindle morphology. In addition, KIF20A was localized at the nucleus of early embryos, and KIF20A inhibition resulted in failure of early parthenogenetic embryo development. These results demonstrated that KIF20A is critical for porcine oocyte meiotic maturation and subsequent early embryo development. |
format | Online Article Text |
id | pubmed-4103861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41038612014-07-21 KIF20A Regulates Porcine Oocyte Maturation and Early Embryo Development Zhang, Yu Liu, Jun Peng, Xu Zhu, Cheng-Cheng Han, Jun Luo, Jia Rui, Rong PLoS One Research Article KIF20A (Kinesin-like family member 20A), also called mitotic kinesin-like proteins 2 (MKLP2), is a mammalian mitotic kinesin-like motor protein of the Kinesin superfamily proteins (KIFs), which was originally involved in Golgi apparatus dynamics and thought to essential for cell cycle regulation during successful cytokinesis. In the present study, we investigated whether KIF20A has roles on porcine oocyte meiotic maturation and subsequent early embryo development. By immunofluorescence staining, KIF20A was found to exhibit a dynamic localization pattern during meiosis. KIF20A was restricted to centromeres after germinal vesicle breakdown (GVBD), transferred to the midbody at telophase I (TI), and again associated with centromeres at metaphase II (MII). Inhibition of endogenous KIF20A via a specific inhibitor, Paprotrain, resulted in failure of polar body extrusion. Further cell cycle analysis showed that the percentage of oocytes that arrested at early metaphase I (MI) stage increased after KIF20A activity inhibition; however, the proportion of oocytes at anaphase/telophase I (ATI) and MII stages decreased significantly. Our results also showed that KIF20A inhibition did not affect spindle morphology. In addition, KIF20A was localized at the nucleus of early embryos, and KIF20A inhibition resulted in failure of early parthenogenetic embryo development. These results demonstrated that KIF20A is critical for porcine oocyte meiotic maturation and subsequent early embryo development. Public Library of Science 2014-07-18 /pmc/articles/PMC4103861/ /pubmed/25036038 http://dx.doi.org/10.1371/journal.pone.0102898 Text en © 2014 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zhang, Yu Liu, Jun Peng, Xu Zhu, Cheng-Cheng Han, Jun Luo, Jia Rui, Rong KIF20A Regulates Porcine Oocyte Maturation and Early Embryo Development |
title | KIF20A Regulates Porcine Oocyte Maturation and Early Embryo Development |
title_full | KIF20A Regulates Porcine Oocyte Maturation and Early Embryo Development |
title_fullStr | KIF20A Regulates Porcine Oocyte Maturation and Early Embryo Development |
title_full_unstemmed | KIF20A Regulates Porcine Oocyte Maturation and Early Embryo Development |
title_short | KIF20A Regulates Porcine Oocyte Maturation and Early Embryo Development |
title_sort | kif20a regulates porcine oocyte maturation and early embryo development |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103861/ https://www.ncbi.nlm.nih.gov/pubmed/25036038 http://dx.doi.org/10.1371/journal.pone.0102898 |
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