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Kinesin-5 Eg5 is essential for spindle assembly and chromosome alignment of mouse spermatocytes

BACKGROUND: Microtubule organization is essential for bipolar spindle assembly and chromosome segregation, which contribute to genome stability. Kinesin-5 Eg5 is known to be a crucial regulator in centrosome separation and spindle assembly in mammalian somatic cells, however, the functions and mecha...

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Autores principales: She, Zhen-Yu, Zhong, Ning, Yu, Kai-Wei, Xiao, Yu, Wei, Ya-Lan, Lin, Yang, Li, Yue-Ling, Lu, Ming-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060529/
https://www.ncbi.nlm.nih.gov/pubmed/32165913
http://dx.doi.org/10.1186/s13008-020-00063-4
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author She, Zhen-Yu
Zhong, Ning
Yu, Kai-Wei
Xiao, Yu
Wei, Ya-Lan
Lin, Yang
Li, Yue-Ling
Lu, Ming-Hui
author_facet She, Zhen-Yu
Zhong, Ning
Yu, Kai-Wei
Xiao, Yu
Wei, Ya-Lan
Lin, Yang
Li, Yue-Ling
Lu, Ming-Hui
author_sort She, Zhen-Yu
collection PubMed
description BACKGROUND: Microtubule organization is essential for bipolar spindle assembly and chromosome segregation, which contribute to genome stability. Kinesin-5 Eg5 is known to be a crucial regulator in centrosome separation and spindle assembly in mammalian somatic cells, however, the functions and mechanisms of Eg5 in male meiotic cell division remain largely unknown. RESULTS: In this study, we have found that Eg5 proteins are expressed in mouse spermatogonia, spermatocytes and spermatids. After Eg5 inhibition by specific inhibitors Monastrol, STLC and Dimethylenastron, the meiotic spindles of dividing spermatocytes show spindle collapse and the defects in bipolar spindle formation. We demonstrate that Eg5 regulates spindle bipolarity and the maintenance of meiotic spindles in meiosis. Eg5 inhibition leads to monopolar spindles, spindle abnormalities and chromosome misalignment in cultured GC-2 spd cells. Furthermore, Eg5 inhibition results in the decrease of the spermatids and the abnormalities in mature sperms. CONCLUSIONS: Our results have revealed an important role of kinesin-5 Eg5 in male meiosis and the maintenance of male fertility. We demonstrate that Eg5 is crucial for bipolar spindle assembly and chromosome alignment in dividing spermatocytes. Our data provide insights into the functions of Eg5 in meiotic spindle assembly of dividing spermatocytes.
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spelling pubmed-70605292020-03-12 Kinesin-5 Eg5 is essential for spindle assembly and chromosome alignment of mouse spermatocytes She, Zhen-Yu Zhong, Ning Yu, Kai-Wei Xiao, Yu Wei, Ya-Lan Lin, Yang Li, Yue-Ling Lu, Ming-Hui Cell Div Research BACKGROUND: Microtubule organization is essential for bipolar spindle assembly and chromosome segregation, which contribute to genome stability. Kinesin-5 Eg5 is known to be a crucial regulator in centrosome separation and spindle assembly in mammalian somatic cells, however, the functions and mechanisms of Eg5 in male meiotic cell division remain largely unknown. RESULTS: In this study, we have found that Eg5 proteins are expressed in mouse spermatogonia, spermatocytes and spermatids. After Eg5 inhibition by specific inhibitors Monastrol, STLC and Dimethylenastron, the meiotic spindles of dividing spermatocytes show spindle collapse and the defects in bipolar spindle formation. We demonstrate that Eg5 regulates spindle bipolarity and the maintenance of meiotic spindles in meiosis. Eg5 inhibition leads to monopolar spindles, spindle abnormalities and chromosome misalignment in cultured GC-2 spd cells. Furthermore, Eg5 inhibition results in the decrease of the spermatids and the abnormalities in mature sperms. CONCLUSIONS: Our results have revealed an important role of kinesin-5 Eg5 in male meiosis and the maintenance of male fertility. We demonstrate that Eg5 is crucial for bipolar spindle assembly and chromosome alignment in dividing spermatocytes. Our data provide insights into the functions of Eg5 in meiotic spindle assembly of dividing spermatocytes. BioMed Central 2020-03-06 /pmc/articles/PMC7060529/ /pubmed/32165913 http://dx.doi.org/10.1186/s13008-020-00063-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
She, Zhen-Yu
Zhong, Ning
Yu, Kai-Wei
Xiao, Yu
Wei, Ya-Lan
Lin, Yang
Li, Yue-Ling
Lu, Ming-Hui
Kinesin-5 Eg5 is essential for spindle assembly and chromosome alignment of mouse spermatocytes
title Kinesin-5 Eg5 is essential for spindle assembly and chromosome alignment of mouse spermatocytes
title_full Kinesin-5 Eg5 is essential for spindle assembly and chromosome alignment of mouse spermatocytes
title_fullStr Kinesin-5 Eg5 is essential for spindle assembly and chromosome alignment of mouse spermatocytes
title_full_unstemmed Kinesin-5 Eg5 is essential for spindle assembly and chromosome alignment of mouse spermatocytes
title_short Kinesin-5 Eg5 is essential for spindle assembly and chromosome alignment of mouse spermatocytes
title_sort kinesin-5 eg5 is essential for spindle assembly and chromosome alignment of mouse spermatocytes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060529/
https://www.ncbi.nlm.nih.gov/pubmed/32165913
http://dx.doi.org/10.1186/s13008-020-00063-4
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