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Gm364 coordinates MIB2/DLL3/Notch2 to regulate female fertility through AKT activation
Many integral membrane proteins might act as indispensable coordinators in specific functional microdomains to maintain the normal operation of known receptors, such as Notch. Gm364 is a multi-pass transmembrane protein that has been screened as a potential female fertility factor. However, there ha...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816931/ https://www.ncbi.nlm.nih.gov/pubmed/34635817 http://dx.doi.org/10.1038/s41418-021-00861-5 |
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author | Chen, Liang-Jian Zhang, Na-Na Zhou, Chun-Xiang Yang, Zhi-Xia Li, Yan-Ru Zhang, Teng Li, Cong-Rong Wang, Xin Wang, Yang Wang, Zi-Bin Xia, Zheng-Rong Wang, Zhen-Bo Zhang, Cui-Lian Guan, Yi-Chun Sun, Qing-Yuan Zhang, Dong |
author_facet | Chen, Liang-Jian Zhang, Na-Na Zhou, Chun-Xiang Yang, Zhi-Xia Li, Yan-Ru Zhang, Teng Li, Cong-Rong Wang, Xin Wang, Yang Wang, Zi-Bin Xia, Zheng-Rong Wang, Zhen-Bo Zhang, Cui-Lian Guan, Yi-Chun Sun, Qing-Yuan Zhang, Dong |
author_sort | Chen, Liang-Jian |
collection | PubMed |
description | Many integral membrane proteins might act as indispensable coordinators in specific functional microdomains to maintain the normal operation of known receptors, such as Notch. Gm364 is a multi-pass transmembrane protein that has been screened as a potential female fertility factor. However, there have been no reports to date about its function in female fertility. Here, we found that global knockout of Gm364 decreased the numbers of primordial follicles and growing follicles, impaired oocyte quality as indicated by increased ROS and γ-H2AX, decreased mitochondrial membrane potential, decreased oocyte maturation, and increased aneuploidy. Mechanistically, Gm364 directly binds and anchors MIB2, a ubiquitin ligase, on the membrane. Subsequently, membrane MIB2 ubiquitinates and activates DLL3. Next, the activated DLL3 binds and activates Notch2, which is subsequently cleaved within the cytoplasm to produce NICD2, the intracellular active domain of Notch2. Finally, NICD2 can directly activate AKT within the cytoplasm to regulate oocyte meiosis and quality. |
format | Online Article Text |
id | pubmed-8816931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88169312022-02-16 Gm364 coordinates MIB2/DLL3/Notch2 to regulate female fertility through AKT activation Chen, Liang-Jian Zhang, Na-Na Zhou, Chun-Xiang Yang, Zhi-Xia Li, Yan-Ru Zhang, Teng Li, Cong-Rong Wang, Xin Wang, Yang Wang, Zi-Bin Xia, Zheng-Rong Wang, Zhen-Bo Zhang, Cui-Lian Guan, Yi-Chun Sun, Qing-Yuan Zhang, Dong Cell Death Differ Article Many integral membrane proteins might act as indispensable coordinators in specific functional microdomains to maintain the normal operation of known receptors, such as Notch. Gm364 is a multi-pass transmembrane protein that has been screened as a potential female fertility factor. However, there have been no reports to date about its function in female fertility. Here, we found that global knockout of Gm364 decreased the numbers of primordial follicles and growing follicles, impaired oocyte quality as indicated by increased ROS and γ-H2AX, decreased mitochondrial membrane potential, decreased oocyte maturation, and increased aneuploidy. Mechanistically, Gm364 directly binds and anchors MIB2, a ubiquitin ligase, on the membrane. Subsequently, membrane MIB2 ubiquitinates and activates DLL3. Next, the activated DLL3 binds and activates Notch2, which is subsequently cleaved within the cytoplasm to produce NICD2, the intracellular active domain of Notch2. Finally, NICD2 can directly activate AKT within the cytoplasm to regulate oocyte meiosis and quality. Nature Publishing Group UK 2021-10-11 2022-02 /pmc/articles/PMC8816931/ /pubmed/34635817 http://dx.doi.org/10.1038/s41418-021-00861-5 Text en © The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chen, Liang-Jian Zhang, Na-Na Zhou, Chun-Xiang Yang, Zhi-Xia Li, Yan-Ru Zhang, Teng Li, Cong-Rong Wang, Xin Wang, Yang Wang, Zi-Bin Xia, Zheng-Rong Wang, Zhen-Bo Zhang, Cui-Lian Guan, Yi-Chun Sun, Qing-Yuan Zhang, Dong Gm364 coordinates MIB2/DLL3/Notch2 to regulate female fertility through AKT activation |
title | Gm364 coordinates MIB2/DLL3/Notch2 to regulate female fertility through AKT activation |
title_full | Gm364 coordinates MIB2/DLL3/Notch2 to regulate female fertility through AKT activation |
title_fullStr | Gm364 coordinates MIB2/DLL3/Notch2 to regulate female fertility through AKT activation |
title_full_unstemmed | Gm364 coordinates MIB2/DLL3/Notch2 to regulate female fertility through AKT activation |
title_short | Gm364 coordinates MIB2/DLL3/Notch2 to regulate female fertility through AKT activation |
title_sort | gm364 coordinates mib2/dll3/notch2 to regulate female fertility through akt activation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816931/ https://www.ncbi.nlm.nih.gov/pubmed/34635817 http://dx.doi.org/10.1038/s41418-021-00861-5 |
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