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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
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.
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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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