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Expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice

The identification and characterization of germ cell-specific genes are essential if we hope to comprehensively understand the mechanisms of spermatogenesis and fertilization. Here, we searched the mouse UniGene databases and identified 13 novel genes as being putatively testis-specific or -predomin...

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Autores principales: Kwon, Jun Tae, Ham, Sera, Jeon, Suyeon, Kim, Youil, Oh, Seungmin, Cho, Chunghee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526581/
https://www.ncbi.nlm.nih.gov/pubmed/28742876
http://dx.doi.org/10.1371/journal.pone.0182038
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author Kwon, Jun Tae
Ham, Sera
Jeon, Suyeon
Kim, Youil
Oh, Seungmin
Cho, Chunghee
author_facet Kwon, Jun Tae
Ham, Sera
Jeon, Suyeon
Kim, Youil
Oh, Seungmin
Cho, Chunghee
author_sort Kwon, Jun Tae
collection PubMed
description The identification and characterization of germ cell-specific genes are essential if we hope to comprehensively understand the mechanisms of spermatogenesis and fertilization. Here, we searched the mouse UniGene databases and identified 13 novel genes as being putatively testis-specific or -predominant. Our in silico and in vitro analyses revealed that the expressions of these genes are testis- and germ cell-specific, and that they are regulated in a stage-specific manner during spermatogenesis. We generated antibodies against the proteins encoded by seven of the genes to facilitate their characterization in male germ cells. Immunoblotting and immunofluorescence analyses revealed that one of these proteins was expressed only in testicular germ cells, three were expressed in both testicular germ cells and testicular sperm, and the remaining three were expressed in sperm of the testicular stages and in mature sperm from the epididymis. Further analysis of the latter three proteins showed that they were all associated with cytoskeletal structures in the sperm flagellum. Among them, MORN5, which is predicted to contain three MORN motifs, is conserved between mouse and human sperm. In conclusion, we herein identify 13 authentic genes with male germ cell-specific expression, and provide comprehensive information about these genes and their encoded products. Our finding will facilitate future investigations into the functional roles of these novel genes in spermatogenesis and sperm functions.
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spelling pubmed-55265812017-08-07 Expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice Kwon, Jun Tae Ham, Sera Jeon, Suyeon Kim, Youil Oh, Seungmin Cho, Chunghee PLoS One Research Article The identification and characterization of germ cell-specific genes are essential if we hope to comprehensively understand the mechanisms of spermatogenesis and fertilization. Here, we searched the mouse UniGene databases and identified 13 novel genes as being putatively testis-specific or -predominant. Our in silico and in vitro analyses revealed that the expressions of these genes are testis- and germ cell-specific, and that they are regulated in a stage-specific manner during spermatogenesis. We generated antibodies against the proteins encoded by seven of the genes to facilitate their characterization in male germ cells. Immunoblotting and immunofluorescence analyses revealed that one of these proteins was expressed only in testicular germ cells, three were expressed in both testicular germ cells and testicular sperm, and the remaining three were expressed in sperm of the testicular stages and in mature sperm from the epididymis. Further analysis of the latter three proteins showed that they were all associated with cytoskeletal structures in the sperm flagellum. Among them, MORN5, which is predicted to contain three MORN motifs, is conserved between mouse and human sperm. In conclusion, we herein identify 13 authentic genes with male germ cell-specific expression, and provide comprehensive information about these genes and their encoded products. Our finding will facilitate future investigations into the functional roles of these novel genes in spermatogenesis and sperm functions. Public Library of Science 2017-07-25 /pmc/articles/PMC5526581/ /pubmed/28742876 http://dx.doi.org/10.1371/journal.pone.0182038 Text en © 2017 Kwon et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kwon, Jun Tae
Ham, Sera
Jeon, Suyeon
Kim, Youil
Oh, Seungmin
Cho, Chunghee
Expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice
title Expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice
title_full Expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice
title_fullStr Expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice
title_full_unstemmed Expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice
title_short Expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice
title_sort expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526581/
https://www.ncbi.nlm.nih.gov/pubmed/28742876
http://dx.doi.org/10.1371/journal.pone.0182038
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