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The vertebrate- and testis- specific transmembrane protein C11ORF94 plays a critical role in sperm-oocyte membrane binding
Sperm-oocyte membrane fusion is necessary for mammalian fertilization. The factors that determine the fusion of sperm with oocytes are largely unknown. So far, spermatozoon factor IZUMO1 and the IZUMO1 counter-receptor JUNO on the oocyte membrane has been identified as a protein requiring fusion. So...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437168/ https://www.ncbi.nlm.nih.gov/pubmed/36050562 http://dx.doi.org/10.1186/s43556-022-00092-1 |
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author | Hao, Hongying Shi, Baolu Zhang, Jiacheng Dai, Ao Li, Wenhao Chen, Haidi Ji, Wenya Gong, Chenjia Zhang, Chang Li, Jing Chen, Li Yao, Bin Hu, Peng Yang, Hao Brosius, Juergen Lai, Shanshan Shi, Qinghua Deng, Cheng |
author_facet | Hao, Hongying Shi, Baolu Zhang, Jiacheng Dai, Ao Li, Wenhao Chen, Haidi Ji, Wenya Gong, Chenjia Zhang, Chang Li, Jing Chen, Li Yao, Bin Hu, Peng Yang, Hao Brosius, Juergen Lai, Shanshan Shi, Qinghua Deng, Cheng |
author_sort | Hao, Hongying |
collection | PubMed |
description | Sperm-oocyte membrane fusion is necessary for mammalian fertilization. The factors that determine the fusion of sperm with oocytes are largely unknown. So far, spermatozoon factor IZUMO1 and the IZUMO1 counter-receptor JUNO on the oocyte membrane has been identified as a protein requiring fusion. Some sperm membrane proteins such as FIMP, SPACA6 and TEME95, have been proved not to directly regulate fusion, but their knockout will affect the fusion process of sperm and oocytes. Here, we identified a novel gene C11orf94 encoding a testicular-specific small transmembrane protein that emerges in vertebrates likely acquired via horizontal gene transfer from bacteria and plays an indispensable role in sperm-oocyte binding. We demonstrated that the deletion of C11orf94 dramatically decreased male fertility in mice. Sperm from C11orf94-deficient mice could pass through the zona pellucida, but failed to bind to the oocyte membrane, thus accumulating in the perivitelline space. In consistence, when the sperm of C11orf94-deficient mice were microinjected into the oocyte cytoplasm, fertilized oocytes were obtained and developed normally to blastocysts. Proteomics analysis revealed that C11orf94 influenced the expression of multiple gene products known to be indispensable for sperm-oocyte binding and fusion, including IZUMO1, EQTN and CRISP1. Thus, our study indicated that C11ORF94 is a vertebrate- and testis-specific small transmembrane protein that plays a critical role in sperm binding to the oolemma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s43556-022-00092-1. |
format | Online Article Text |
id | pubmed-9437168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-94371682022-09-03 The vertebrate- and testis- specific transmembrane protein C11ORF94 plays a critical role in sperm-oocyte membrane binding Hao, Hongying Shi, Baolu Zhang, Jiacheng Dai, Ao Li, Wenhao Chen, Haidi Ji, Wenya Gong, Chenjia Zhang, Chang Li, Jing Chen, Li Yao, Bin Hu, Peng Yang, Hao Brosius, Juergen Lai, Shanshan Shi, Qinghua Deng, Cheng Mol Biomed Research Sperm-oocyte membrane fusion is necessary for mammalian fertilization. The factors that determine the fusion of sperm with oocytes are largely unknown. So far, spermatozoon factor IZUMO1 and the IZUMO1 counter-receptor JUNO on the oocyte membrane has been identified as a protein requiring fusion. Some sperm membrane proteins such as FIMP, SPACA6 and TEME95, have been proved not to directly regulate fusion, but their knockout will affect the fusion process of sperm and oocytes. Here, we identified a novel gene C11orf94 encoding a testicular-specific small transmembrane protein that emerges in vertebrates likely acquired via horizontal gene transfer from bacteria and plays an indispensable role in sperm-oocyte binding. We demonstrated that the deletion of C11orf94 dramatically decreased male fertility in mice. Sperm from C11orf94-deficient mice could pass through the zona pellucida, but failed to bind to the oocyte membrane, thus accumulating in the perivitelline space. In consistence, when the sperm of C11orf94-deficient mice were microinjected into the oocyte cytoplasm, fertilized oocytes were obtained and developed normally to blastocysts. Proteomics analysis revealed that C11orf94 influenced the expression of multiple gene products known to be indispensable for sperm-oocyte binding and fusion, including IZUMO1, EQTN and CRISP1. Thus, our study indicated that C11ORF94 is a vertebrate- and testis-specific small transmembrane protein that plays a critical role in sperm binding to the oolemma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s43556-022-00092-1. Springer Nature Singapore 2022-09-02 /pmc/articles/PMC9437168/ /pubmed/36050562 http://dx.doi.org/10.1186/s43556-022-00092-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Hao, Hongying Shi, Baolu Zhang, Jiacheng Dai, Ao Li, Wenhao Chen, Haidi Ji, Wenya Gong, Chenjia Zhang, Chang Li, Jing Chen, Li Yao, Bin Hu, Peng Yang, Hao Brosius, Juergen Lai, Shanshan Shi, Qinghua Deng, Cheng The vertebrate- and testis- specific transmembrane protein C11ORF94 plays a critical role in sperm-oocyte membrane binding |
title | The vertebrate- and testis- specific transmembrane protein C11ORF94 plays a critical role in sperm-oocyte membrane binding |
title_full | The vertebrate- and testis- specific transmembrane protein C11ORF94 plays a critical role in sperm-oocyte membrane binding |
title_fullStr | The vertebrate- and testis- specific transmembrane protein C11ORF94 plays a critical role in sperm-oocyte membrane binding |
title_full_unstemmed | The vertebrate- and testis- specific transmembrane protein C11ORF94 plays a critical role in sperm-oocyte membrane binding |
title_short | The vertebrate- and testis- specific transmembrane protein C11ORF94 plays a critical role in sperm-oocyte membrane binding |
title_sort | vertebrate- and testis- specific transmembrane protein c11orf94 plays a critical role in sperm-oocyte membrane binding |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437168/ https://www.ncbi.nlm.nih.gov/pubmed/36050562 http://dx.doi.org/10.1186/s43556-022-00092-1 |
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