Cargando…

Spermatozoa lacking Fertilization Influencing Membrane Protein (FIMP) fail to fuse with oocytes in mice

Sperm–oocyte fusion is a critical event in mammalian fertilization, categorized by three indispensable proteins. Sperm membrane protein IZUMO1 and its counterpart oocyte membrane protein JUNO make a protein complex allowing sperm to interact with the oocyte, and subsequent sperm–oocyte fusion. Oocyt...

Descripción completa

Detalles Bibliográficos
Autores principales: Fujihara, Yoshitaka, Lu, Yonggang, Noda, Taichi, Oji, Asami, Larasati, Tamara, Kojima-Kita, Kanako, Yu, Zhifeng, Matzuk, Ryan M., Matzuk, Martin M., Ikawa, Masahito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196805/
https://www.ncbi.nlm.nih.gov/pubmed/32295885
http://dx.doi.org/10.1073/pnas.1917060117
_version_ 1783528776324349952
author Fujihara, Yoshitaka
Lu, Yonggang
Noda, Taichi
Oji, Asami
Larasati, Tamara
Kojima-Kita, Kanako
Yu, Zhifeng
Matzuk, Ryan M.
Matzuk, Martin M.
Ikawa, Masahito
author_facet Fujihara, Yoshitaka
Lu, Yonggang
Noda, Taichi
Oji, Asami
Larasati, Tamara
Kojima-Kita, Kanako
Yu, Zhifeng
Matzuk, Ryan M.
Matzuk, Martin M.
Ikawa, Masahito
author_sort Fujihara, Yoshitaka
collection PubMed
description Sperm–oocyte fusion is a critical event in mammalian fertilization, categorized by three indispensable proteins. Sperm membrane protein IZUMO1 and its counterpart oocyte membrane protein JUNO make a protein complex allowing sperm to interact with the oocyte, and subsequent sperm–oocyte fusion. Oocyte tetraspanin protein CD9 also contributes to sperm–oocyte fusion. However, the fusion process cannot be explained solely by these three essential factors. In this study, we focused on analyzing a testis-specific gene 4930451I11Rik and generated mutant mice using the CRISPR/Cas9 system. Although IZUMO1 remained in 4930451I11Rik knockout (KO) spermatozoa, the KO spermatozoa were unable to fuse with oocytes and the KO males were severely subfertile. 4930451I11Rik encodes two isoforms: a transmembrane (TM) form and a secreted form. Both CRISPR/Cas9-mediated TM deletion and transgenic (Tg) rescue with the TM form revealed that only the TM form plays a critical role in sperm–oocyte fusion. Thus, we renamed this TM form Fertilization Influencing Membrane Protein (FIMP). The mCherry-tagged FIMP TM form was localized to the sperm equatorial segment where the sperm–oocyte fusion event occurs. Thus, FIMP is a sperm-specific transmembrane protein that is necessary for the sperm–oocyte fusion process.
format Online
Article
Text
id pubmed-7196805
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-71968052020-05-06 Spermatozoa lacking Fertilization Influencing Membrane Protein (FIMP) fail to fuse with oocytes in mice Fujihara, Yoshitaka Lu, Yonggang Noda, Taichi Oji, Asami Larasati, Tamara Kojima-Kita, Kanako Yu, Zhifeng Matzuk, Ryan M. Matzuk, Martin M. Ikawa, Masahito Proc Natl Acad Sci U S A Biological Sciences Sperm–oocyte fusion is a critical event in mammalian fertilization, categorized by three indispensable proteins. Sperm membrane protein IZUMO1 and its counterpart oocyte membrane protein JUNO make a protein complex allowing sperm to interact with the oocyte, and subsequent sperm–oocyte fusion. Oocyte tetraspanin protein CD9 also contributes to sperm–oocyte fusion. However, the fusion process cannot be explained solely by these three essential factors. In this study, we focused on analyzing a testis-specific gene 4930451I11Rik and generated mutant mice using the CRISPR/Cas9 system. Although IZUMO1 remained in 4930451I11Rik knockout (KO) spermatozoa, the KO spermatozoa were unable to fuse with oocytes and the KO males were severely subfertile. 4930451I11Rik encodes two isoforms: a transmembrane (TM) form and a secreted form. Both CRISPR/Cas9-mediated TM deletion and transgenic (Tg) rescue with the TM form revealed that only the TM form plays a critical role in sperm–oocyte fusion. Thus, we renamed this TM form Fertilization Influencing Membrane Protein (FIMP). The mCherry-tagged FIMP TM form was localized to the sperm equatorial segment where the sperm–oocyte fusion event occurs. Thus, FIMP is a sperm-specific transmembrane protein that is necessary for the sperm–oocyte fusion process. National Academy of Sciences 2020-04-28 2020-04-15 /pmc/articles/PMC7196805/ /pubmed/32295885 http://dx.doi.org/10.1073/pnas.1917060117 Text en Copyright © 2020 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Fujihara, Yoshitaka
Lu, Yonggang
Noda, Taichi
Oji, Asami
Larasati, Tamara
Kojima-Kita, Kanako
Yu, Zhifeng
Matzuk, Ryan M.
Matzuk, Martin M.
Ikawa, Masahito
Spermatozoa lacking Fertilization Influencing Membrane Protein (FIMP) fail to fuse with oocytes in mice
title Spermatozoa lacking Fertilization Influencing Membrane Protein (FIMP) fail to fuse with oocytes in mice
title_full Spermatozoa lacking Fertilization Influencing Membrane Protein (FIMP) fail to fuse with oocytes in mice
title_fullStr Spermatozoa lacking Fertilization Influencing Membrane Protein (FIMP) fail to fuse with oocytes in mice
title_full_unstemmed Spermatozoa lacking Fertilization Influencing Membrane Protein (FIMP) fail to fuse with oocytes in mice
title_short Spermatozoa lacking Fertilization Influencing Membrane Protein (FIMP) fail to fuse with oocytes in mice
title_sort spermatozoa lacking fertilization influencing membrane protein (fimp) fail to fuse with oocytes in mice
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196805/
https://www.ncbi.nlm.nih.gov/pubmed/32295885
http://dx.doi.org/10.1073/pnas.1917060117
work_keys_str_mv AT fujiharayoshitaka spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice
AT luyonggang spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice
AT nodataichi spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice
AT ojiasami spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice
AT larasatitamara spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice
AT kojimakitakanako spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice
AT yuzhifeng spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice
AT matzukryanm spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice
AT matzukmartinm spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice
AT ikawamasahito spermatozoalackingfertilizationinfluencingmembraneproteinfimpfailtofusewithoocytesinmice