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TBC1D21 Potentially Interacts with and Regulates Rap1 during Murine Spermatogenesis
Few papers have focused on small guanosine triphosphate (GTP)-binding proteins and their regulation during spermatogenesis. TBC1D21 genes (also known as male germ cell RAB GTPase-activating protein MGCRABGAP) are related to sterility, as determined through cDNA microarray testing of human testicular...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274753/ https://www.ncbi.nlm.nih.gov/pubmed/30360518 http://dx.doi.org/10.3390/ijms19113292 |
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author | Ke, Chih-Chun Lin, Ying-Hung Wang, Ya-Yun Wu, Ying-Yu Chen, Mei-Feng Ku, Wei-Chi Chiang, Han-Sun Lai, Tsung-Hsuan |
author_facet | Ke, Chih-Chun Lin, Ying-Hung Wang, Ya-Yun Wu, Ying-Yu Chen, Mei-Feng Ku, Wei-Chi Chiang, Han-Sun Lai, Tsung-Hsuan |
author_sort | Ke, Chih-Chun |
collection | PubMed |
description | Few papers have focused on small guanosine triphosphate (GTP)-binding proteins and their regulation during spermatogenesis. TBC1D21 genes (also known as male germ cell RAB GTPase-activating protein MGCRABGAP) are related to sterility, as determined through cDNA microarray testing of human testicular tissues exhibiting spermatogenic defects. TBC1D21 is a protein specifically expressed in the testes that exhibits specific localizations of elongating and elongated spermatids during mammalian spermiogenesis. Furthermore, through co-immunoprecipitation (co-IP) and nano liquid chromatography–tandem mass spectrometry (nano LC–MS/MS), Rap1 has been recognized as a potential TBC1D21 interactor. This study determined the possible roles of Rap1 and TBC1D21 during mammalian spermiogenesis. First, the binding ability between Rap1 and TBC1D21 was verified using co-IP. Second, the stronger signals of Rap1 expressed in elongating and elongated murine spermatids extracted from testicular sections, namely spermatogonia, spermatocytes, and round spermatids, were compared. Third, Rap1 and TBC1D21 exhibited similar localizations at postacrosomal regions of spermatids and at the midpieces of mature sperms, through isolated male germ cells. Fourth, the results of an activating Rap1 pull-down assay indicated that TBC1D21 overexpression inactivates Rap1 activity in cell models. In conclusion, TBC1D21 may interact with and potentially regulate Rap1 during murine spermatogenesis. |
format | Online Article Text |
id | pubmed-6274753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62747532018-12-15 TBC1D21 Potentially Interacts with and Regulates Rap1 during Murine Spermatogenesis Ke, Chih-Chun Lin, Ying-Hung Wang, Ya-Yun Wu, Ying-Yu Chen, Mei-Feng Ku, Wei-Chi Chiang, Han-Sun Lai, Tsung-Hsuan Int J Mol Sci Article Few papers have focused on small guanosine triphosphate (GTP)-binding proteins and their regulation during spermatogenesis. TBC1D21 genes (also known as male germ cell RAB GTPase-activating protein MGCRABGAP) are related to sterility, as determined through cDNA microarray testing of human testicular tissues exhibiting spermatogenic defects. TBC1D21 is a protein specifically expressed in the testes that exhibits specific localizations of elongating and elongated spermatids during mammalian spermiogenesis. Furthermore, through co-immunoprecipitation (co-IP) and nano liquid chromatography–tandem mass spectrometry (nano LC–MS/MS), Rap1 has been recognized as a potential TBC1D21 interactor. This study determined the possible roles of Rap1 and TBC1D21 during mammalian spermiogenesis. First, the binding ability between Rap1 and TBC1D21 was verified using co-IP. Second, the stronger signals of Rap1 expressed in elongating and elongated murine spermatids extracted from testicular sections, namely spermatogonia, spermatocytes, and round spermatids, were compared. Third, Rap1 and TBC1D21 exhibited similar localizations at postacrosomal regions of spermatids and at the midpieces of mature sperms, through isolated male germ cells. Fourth, the results of an activating Rap1 pull-down assay indicated that TBC1D21 overexpression inactivates Rap1 activity in cell models. In conclusion, TBC1D21 may interact with and potentially regulate Rap1 during murine spermatogenesis. MDPI 2018-10-23 /pmc/articles/PMC6274753/ /pubmed/30360518 http://dx.doi.org/10.3390/ijms19113292 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ke, Chih-Chun Lin, Ying-Hung Wang, Ya-Yun Wu, Ying-Yu Chen, Mei-Feng Ku, Wei-Chi Chiang, Han-Sun Lai, Tsung-Hsuan TBC1D21 Potentially Interacts with and Regulates Rap1 during Murine Spermatogenesis |
title | TBC1D21 Potentially Interacts with and Regulates Rap1 during Murine Spermatogenesis |
title_full | TBC1D21 Potentially Interacts with and Regulates Rap1 during Murine Spermatogenesis |
title_fullStr | TBC1D21 Potentially Interacts with and Regulates Rap1 during Murine Spermatogenesis |
title_full_unstemmed | TBC1D21 Potentially Interacts with and Regulates Rap1 during Murine Spermatogenesis |
title_short | TBC1D21 Potentially Interacts with and Regulates Rap1 during Murine Spermatogenesis |
title_sort | tbc1d21 potentially interacts with and regulates rap1 during murine spermatogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274753/ https://www.ncbi.nlm.nih.gov/pubmed/30360518 http://dx.doi.org/10.3390/ijms19113292 |
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