Lin Ying-Hung, Ke Chih-Chun, Wang Ya-Yun, Chen Mei-Feng, Chen Tsung-Ming, Ku Wei-Chi, Chiang Han-Sun, Yeh Chung-Hsin
Graduate Institute of Biomedical and Pharmaceutical Science, Fu-Jen Catholic University, New Taipei City 24205, Taiwan.
Department of Urology, En Chu Kong Hospital, New Taipei City 23702, Taiwan.
Int J Mol Sci. 2017 Jan 5;18(1):97. doi: 10.3390/ijms18010097.
According to recent estimates, 2%-15% of couples are sterile, and approximately half of the infertility cases are attributed to male reproductive factors. However, the reasons remain undefined in approximately 25% of male infertility cases, and most infertility cases exhibit spermatogenic defects. Numerous genes involved in spermatogenesis still remain unknown. We previously identified () through cDNA microarray analysis of human testicular tissues with spermatogenic defects. MGCRABGAP contains a conserved RABGAP catalytic domain, TBC (Tre2/Bub2/Cdc16). RABGAP family proteins regulate cellular function (e.g., cytoskeletal remodeling, vesicular trafficking, and cell migration) by inactivating RAB proteins. MGCRABGAP is a male germ cell-specific protein expressed in elongating and elongated spermatids during mammalian spermiogenesis. The purpose of this study was to identify proteins that interact with MGCRABGAP during mammalian spermiogenesis using a proteomic approach. We found that MGCRABGAP exhibited GTPase-activating bioability, and several MGCRABGAP interactors, possible substrates (e.g., RAB10, RAB5C, and RAP1), were identified using co-immunoprecipitation (co-IP) and nano liquid chromatography-mass spectrometry/mass spectrometry (nano LC-MS/MS). We confirmed the binding ability between RAB10 and MGCRABGAP via co-IP. Additionally, MGCRABGAP-RAB10 complexes were specifically colocalized in the manchette structure, a critical structure for the formation of spermatid heads, and were slightly expressed at the midpiece of mature spermatozoa. Based on these results, we propose that MGCRABGAP is involved in mammalian spermiogenesis by modulating RAB10.
根据最近的估计,2% - 15%的夫妇患有不育症,并且大约一半的不育病例归因于男性生殖因素。然而,在大约25%的男性不育病例中,病因仍不明确,并且大多数不育病例表现出精子发生缺陷。许多参与精子发生的基因仍然未知。我们之前通过对有精子发生缺陷的人类睾丸组织进行cDNA微阵列分析,鉴定出了()。MGCRABGAP包含一个保守的RABGAP催化结构域,即TBC(Tre2/Bub2/Cdc16)。RABGAP家族蛋白通过使RAB蛋白失活来调节细胞功能(例如,细胞骨架重塑、囊泡运输和细胞迁移)。MGCRABGAP是一种雄性生殖细胞特异性蛋白,在哺乳动物精子形成过程中的延长和延长型精子细胞中表达。本研究的目的是使用蛋白质组学方法鉴定在哺乳动物精子形成过程中与MGCRABGAP相互作用的蛋白质。我们发现MGCRABGAP具有GTP酶激活生物活性,并且使用免疫共沉淀(co - IP)和纳升液相色谱 - 质谱联用/质谱(nano LC - MS/MS)鉴定出了几种MGCRABGAP相互作用蛋白,即可能的底物(例如,RAB10、RAB5C和RAP1)。我们通过co - IP证实了RAB10与MGCRABGAP之间的结合能力。此外,MGCRABGAP - RAB10复合物特异性地共定位于精子细胞头部形成的关键结构——环带结构中,并且在成熟精子的中段有少量表达。基于这些结果,我们提出MGCRABGAP通过调节RAB10参与哺乳动物精子形成过程。