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Tropomodulin-3 is essential in asymmetric division during mouse oocyte maturation
The dynamic polymerization and depolymerization of actin filaments is essential for various cellular processes such as cell migration, rotation, cytokinesis, and mammalian oocyte maturation. Tropomodulin 3 (Tmod3) binds to the slow-growing (pointed) ends of the actin filament, thereby protecting the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931587/ https://www.ncbi.nlm.nih.gov/pubmed/27374327 http://dx.doi.org/10.1038/srep29204 |
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author | Jo, Yu-Jin Jang, Woo-In Kim, Nam-Hyung Namgoong, Suk |
author_facet | Jo, Yu-Jin Jang, Woo-In Kim, Nam-Hyung Namgoong, Suk |
author_sort | Jo, Yu-Jin |
collection | PubMed |
description | The dynamic polymerization and depolymerization of actin filaments is essential for various cellular processes such as cell migration, rotation, cytokinesis, and mammalian oocyte maturation. Tropomodulin 3 (Tmod3) binds to the slow-growing (pointed) ends of the actin filament, thereby protecting the filament from depolymerization. However, the roles of Tmod3 in mammalian oocyte maturation remain elusive. Tmod3 mRNA and protein is present at all stages of mouse oocyte maturation. Tmod3 protein is mainly localized in the cytoplasm and appears enriched near the chromosome during maturation. By knocking down or ectopically overexpressing Tmod3, we confirmed that Tmod3 regulate the level of the intracytoplasmic actin mesh and asymmetric spindle migration. Expression of N-terminal Tmod3 (correspond to 1–155 amino acids), which contains the tropomyosin-binding site, results in decreased density of the actin mesh, thereby demonstrating the importance of the interaction between tropomyosin and tropomodulin for the maintenance of the actin mesh. Taken together, these findings indicate that Tmod3 plays crucial roles in oocyte maturation, presumably by protecting the actin filament from depolymerization and thereby controlling the density of the cytoplasmic actin mesh. |
format | Online Article Text |
id | pubmed-4931587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49315872016-07-06 Tropomodulin-3 is essential in asymmetric division during mouse oocyte maturation Jo, Yu-Jin Jang, Woo-In Kim, Nam-Hyung Namgoong, Suk Sci Rep Article The dynamic polymerization and depolymerization of actin filaments is essential for various cellular processes such as cell migration, rotation, cytokinesis, and mammalian oocyte maturation. Tropomodulin 3 (Tmod3) binds to the slow-growing (pointed) ends of the actin filament, thereby protecting the filament from depolymerization. However, the roles of Tmod3 in mammalian oocyte maturation remain elusive. Tmod3 mRNA and protein is present at all stages of mouse oocyte maturation. Tmod3 protein is mainly localized in the cytoplasm and appears enriched near the chromosome during maturation. By knocking down or ectopically overexpressing Tmod3, we confirmed that Tmod3 regulate the level of the intracytoplasmic actin mesh and asymmetric spindle migration. Expression of N-terminal Tmod3 (correspond to 1–155 amino acids), which contains the tropomyosin-binding site, results in decreased density of the actin mesh, thereby demonstrating the importance of the interaction between tropomyosin and tropomodulin for the maintenance of the actin mesh. Taken together, these findings indicate that Tmod3 plays crucial roles in oocyte maturation, presumably by protecting the actin filament from depolymerization and thereby controlling the density of the cytoplasmic actin mesh. Nature Publishing Group 2016-07-04 /pmc/articles/PMC4931587/ /pubmed/27374327 http://dx.doi.org/10.1038/srep29204 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jo, Yu-Jin Jang, Woo-In Kim, Nam-Hyung Namgoong, Suk Tropomodulin-3 is essential in asymmetric division during mouse oocyte maturation |
title | Tropomodulin-3 is essential in asymmetric division during mouse oocyte maturation |
title_full | Tropomodulin-3 is essential in asymmetric division during mouse oocyte maturation |
title_fullStr | Tropomodulin-3 is essential in asymmetric division during mouse oocyte maturation |
title_full_unstemmed | Tropomodulin-3 is essential in asymmetric division during mouse oocyte maturation |
title_short | Tropomodulin-3 is essential in asymmetric division during mouse oocyte maturation |
title_sort | tropomodulin-3 is essential in asymmetric division during mouse oocyte maturation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931587/ https://www.ncbi.nlm.nih.gov/pubmed/27374327 http://dx.doi.org/10.1038/srep29204 |
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