TBC1D21 Potentially Interacts with and Regulates Rap1 during Murine Spermatogenesis

被引:14
作者
Ke, Chih-Chun [1 ,2 ]
Lin, Ying-Hung [3 ]
Wang, Ya-Yun [4 ]
Wu, Ying-Yu [3 ]
Chen, Mei-Feng [5 ]
Ku, Wei-Chi [6 ]
Chiang, Han-Sun [3 ]
Lai, Tsung-Hsuan [6 ,7 ,8 ]
机构
[1] Fu Jen Catholic Univ, PhD Program Nutr & Food Sci, New Taipei 24205, Taiwan
[2] En Chu Kong Hosp, Dept Urol, New Taipei 23702, Taiwan
[3] Fu Jen Catholic Univ, Grad Inst Biomed & Pharmaceut Sci, New Taipei 24205, Taiwan
[4] Fu Jen Catholic Univ, Dept Chem, New Taipei 24205, Taiwan
[5] Chang Gung Mem Hosp, Bone & Joint Res Ctr, Gueishan Township 33305, Taoyuan County, Taiwan
[6] Fu Jen Catholic Univ, Sch Med, New Taipei 24205, Taiwan
[7] Cathay Gen Hosp, Dept Obstet & Gynecol, Taipei 10630, Taiwan
[8] Natl Cent Univ, Inst Syst Biol & Bioinformat, Jhongli 32001, Taoyuan County, Taiwan
关键词
Rap1; TBC1D21; spermatids; male infertility; GTPASE-ACTIVATING PROTEIN; MEIOTIC CELL-CYCLES; EXPRESSION; IDENTIFICATION; LOCALIZATION; INFERTILITY; FERTILITY; GROWTH; GENES; GAPS;
D O I
10.3390/ijms19113292
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页数:10
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