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Rac1 is dispensable for oocyte maturation and female fertility in vivo

Oocyte maturation, the important process to produce female haploid gamete, accompanies with polarity establishment and highly asymmetric cell division to emit minor polar body within little cytoplasm. Microfilaments play central roles in polarity establishment and asymmetric cell division. Several a...

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Autores principales: Hao, Jian-Xiu, Meng, Tie-Gang, Fan, Li-Hua, Yao, Yuan-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436689/
https://www.ncbi.nlm.nih.gov/pubmed/28545113
http://dx.doi.org/10.1371/journal.pone.0177202
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author Hao, Jian-Xiu
Meng, Tie-Gang
Fan, Li-Hua
Yao, Yuan-Qing
author_facet Hao, Jian-Xiu
Meng, Tie-Gang
Fan, Li-Hua
Yao, Yuan-Qing
author_sort Hao, Jian-Xiu
collection PubMed
description Oocyte maturation, the important process to produce female haploid gamete, accompanies with polarity establishment and highly asymmetric cell division to emit minor polar body within little cytoplasm. Microfilaments play central roles in polarity establishment and asymmetric cell division. Several actin regulators like WASP protein family as well as small GTPases function in microfilament dynamics, involving the process. Rac1, one member of RhoGTPases, has been reported to regulate the polarity and asymmetric cell division in mouse oocytes in vitro. The physiological role of Rac1 in mouse oocyte remains unknown. By conditional knockout technology, we specifically deleted Rac1 gene in mouse oocyte, and found that Rac1 deletion exerted little effect on mouse oocyte maturation including polarity establishment and asymmetric division, and the mutant mice showed normal fertility.
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spelling pubmed-54366892017-05-27 Rac1 is dispensable for oocyte maturation and female fertility in vivo Hao, Jian-Xiu Meng, Tie-Gang Fan, Li-Hua Yao, Yuan-Qing PLoS One Research Article Oocyte maturation, the important process to produce female haploid gamete, accompanies with polarity establishment and highly asymmetric cell division to emit minor polar body within little cytoplasm. Microfilaments play central roles in polarity establishment and asymmetric cell division. Several actin regulators like WASP protein family as well as small GTPases function in microfilament dynamics, involving the process. Rac1, one member of RhoGTPases, has been reported to regulate the polarity and asymmetric cell division in mouse oocytes in vitro. The physiological role of Rac1 in mouse oocyte remains unknown. By conditional knockout technology, we specifically deleted Rac1 gene in mouse oocyte, and found that Rac1 deletion exerted little effect on mouse oocyte maturation including polarity establishment and asymmetric division, and the mutant mice showed normal fertility. Public Library of Science 2017-05-18 /pmc/articles/PMC5436689/ /pubmed/28545113 http://dx.doi.org/10.1371/journal.pone.0177202 Text en © 2017 Hao 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hao, Jian-Xiu
Meng, Tie-Gang
Fan, Li-Hua
Yao, Yuan-Qing
Rac1 is dispensable for oocyte maturation and female fertility in vivo
title Rac1 is dispensable for oocyte maturation and female fertility in vivo
title_full Rac1 is dispensable for oocyte maturation and female fertility in vivo
title_fullStr Rac1 is dispensable for oocyte maturation and female fertility in vivo
title_full_unstemmed Rac1 is dispensable for oocyte maturation and female fertility in vivo
title_short Rac1 is dispensable for oocyte maturation and female fertility in vivo
title_sort rac1 is dispensable for oocyte maturation and female fertility in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436689/
https://www.ncbi.nlm.nih.gov/pubmed/28545113
http://dx.doi.org/10.1371/journal.pone.0177202
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