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HUWE1 plays important role in mouse preimplantation embryo development and the dysregulation is associated with poor embryo development in humans
HUWE1 is a HECT domain containing ubiquitin ligase implicated in neurogenesis, spermatogenesis and cancer development. The purpose of the current study is to investigate the role of HUWE1 in early embryo development. Here we demonstrate that Huwe1 is expressed in both nucleus and cytoplasm of preimp...
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/PMC5128802/ https://www.ncbi.nlm.nih.gov/pubmed/27901130 http://dx.doi.org/10.1038/srep37928 |
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author | Chen, L. J. Xu, W. M. Yang, M. Wang, K. Chen, Y. Huang, X. J. Ma, Q. H. |
author_facet | Chen, L. J. Xu, W. M. Yang, M. Wang, K. Chen, Y. Huang, X. J. Ma, Q. H. |
author_sort | Chen, L. J. |
collection | PubMed |
description | HUWE1 is a HECT domain containing ubiquitin ligase implicated in neurogenesis, spermatogenesis and cancer development. The purpose of the current study is to investigate the role of HUWE1 in early embryo development. Here we demonstrate that Huwe1 is expressed in both nucleus and cytoplasm of preimplantation mouse embryos as well as gametes. Hypoxia (5% O(2)) treatment could significantly increase Huwe1 expression during mouse embryo development process. HUWE1 knockdown inhibited normal embryonic development and reduced blastocyst formation, and increased apoptotic cell numbers were observed in the embryos of HUWE1 knockdown group. Human embryo staining result showed that reduced HUWE1 staining was observed in the poor-quality embryos. Furthermore, Western blot result showed that significantly reduced expression of HUWE1 was observed in the villi of miscarriage embryos compared with the normal control, indicating that reduced expression of HUWE1 is related to poor embryo development. Oxidative reagent, H(2)O(2) inhibited HUWE1 expression in human sperm, indicating that HUWE1 expression in sperm is regulated by oxidative stress. In conclusion, these results suggest that HUWE1 protein could contribute to preimplantation embryo development and dysregulated expression of HUWE1 could be related to poor embryo development and miscarriage in IVF clinic. |
format | Online Article Text |
id | pubmed-5128802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51288022016-12-09 HUWE1 plays important role in mouse preimplantation embryo development and the dysregulation is associated with poor embryo development in humans Chen, L. J. Xu, W. M. Yang, M. Wang, K. Chen, Y. Huang, X. J. Ma, Q. H. Sci Rep Article HUWE1 is a HECT domain containing ubiquitin ligase implicated in neurogenesis, spermatogenesis and cancer development. The purpose of the current study is to investigate the role of HUWE1 in early embryo development. Here we demonstrate that Huwe1 is expressed in both nucleus and cytoplasm of preimplantation mouse embryos as well as gametes. Hypoxia (5% O(2)) treatment could significantly increase Huwe1 expression during mouse embryo development process. HUWE1 knockdown inhibited normal embryonic development and reduced blastocyst formation, and increased apoptotic cell numbers were observed in the embryos of HUWE1 knockdown group. Human embryo staining result showed that reduced HUWE1 staining was observed in the poor-quality embryos. Furthermore, Western blot result showed that significantly reduced expression of HUWE1 was observed in the villi of miscarriage embryos compared with the normal control, indicating that reduced expression of HUWE1 is related to poor embryo development. Oxidative reagent, H(2)O(2) inhibited HUWE1 expression in human sperm, indicating that HUWE1 expression in sperm is regulated by oxidative stress. In conclusion, these results suggest that HUWE1 protein could contribute to preimplantation embryo development and dysregulated expression of HUWE1 could be related to poor embryo development and miscarriage in IVF clinic. Nature Publishing Group 2016-11-30 /pmc/articles/PMC5128802/ /pubmed/27901130 http://dx.doi.org/10.1038/srep37928 Text en Copyright © 2016, The Author(s) 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 Chen, L. J. Xu, W. M. Yang, M. Wang, K. Chen, Y. Huang, X. J. Ma, Q. H. HUWE1 plays important role in mouse preimplantation embryo development and the dysregulation is associated with poor embryo development in humans |
title | HUWE1 plays important role in mouse preimplantation embryo development and the dysregulation is associated with poor embryo development in humans |
title_full | HUWE1 plays important role in mouse preimplantation embryo development and the dysregulation is associated with poor embryo development in humans |
title_fullStr | HUWE1 plays important role in mouse preimplantation embryo development and the dysregulation is associated with poor embryo development in humans |
title_full_unstemmed | HUWE1 plays important role in mouse preimplantation embryo development and the dysregulation is associated with poor embryo development in humans |
title_short | HUWE1 plays important role in mouse preimplantation embryo development and the dysregulation is associated with poor embryo development in humans |
title_sort | huwe1 plays important role in mouse preimplantation embryo development and the dysregulation is associated with poor embryo development in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128802/ https://www.ncbi.nlm.nih.gov/pubmed/27901130 http://dx.doi.org/10.1038/srep37928 |
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