Park Yoo-Jin, Pang Won-Ki, Ryu Do-Yeal, Rahman Md Saidur, Pang Myung-Geol
Department of Animal Science & Technology and BET Research Institute, Chung-Ang University, Anseong, Gyeonggi-do 17546, Republic of Korea.
Department of Animal Science & Technology and BET Research Institute, Chung-Ang University, Anseong, Gyeonggi-do 17546, Republic of Korea.
J Adv Res. 2025 Mar 18. doi: 10.1016/j.jare.2025.03.035.
Despite the lack of essential cytoplasmic organelles in mature spermatozoa, which creates unfavorable conditions for transcription and translation, the presence of various mRNA and proteins during capacitation suggests potential for de novo protein synthesis.
We applied a metabolic labeling method using a fluorescent noncanonical amino acid tagging system (FUNCAT) and proximity ligation method (PLA) in normal and reduced fertility spermatozoa to detect different translation phenomena during sperm capacitation according to their fertility.
We explored different proteome changes in spermatozoa according to the time-sequential capacitation process (0, 20, 40, 60, and 120 min) between normal [average fertility rate (FR) = 77.44 % ± 1.51] and reduced fertility (average FR = 58.57 % ± 1.64) spermatozoa bull spermatozoa, as the representative male fertility models owing to their broad spectrum of fertility phenotypes. Moreover, the FUNCAT/PLA method was used to detect and visualize different translation phenomena during sperm capacitation according to fertility.
We found that sperm-associated protein (SPACA) 1 and SPACA5 were newly synthesized in the head of normal-fertility spermatozoa, whereas a lack of newly synthesized proteins in the head and a relatively earlier loss of SPACA1 and SPACA5 were observed in the reduced-fertility spermatozoa. Moreover, the mitochondrial translation inhibitor, chloramphenicol, partially inhibited sperm translation and delayed translocation, suggesting that mitochondria participate in sperm translation.
Our results unveil time-sequential microenvironmental changes in sperm proteomes during capacitation, which lead to the orchestra of proteins that complete fertilization. Fertile spermatozoa are selected through inter-competition during the journey of fertilization in the female reproductive tract. This study provides an overview of how translation dynamics acts on the sperm selection and influence the evolution of sperm fertility.
尽管成熟精子缺乏必需的细胞质细胞器,这为转录和翻译创造了不利条件,但获能过程中各种mRNA和蛋白质的存在表明其具有从头合成蛋白质的潜力。
我们应用一种使用荧光非经典氨基酸标记系统(FUNCAT)的代谢标记方法和邻近连接法(PLA),对正常生育力和生育力降低的精子进行检测,以根据其生育力检测精子获能过程中不同的翻译现象。
我们研究了正常生育力(平均生育率[FR]=77.44%±1.51)和生育力降低(平均FR=58.57%±1.64)的公牛精子在按时间顺序排列的获能过程(0、20、40、60和120分钟)中精子蛋白质组的不同变化,公牛精子作为具有广泛生育力表型的代表性雄性生育模型。此外,使用FUNCAT/PLA方法根据生育力检测和可视化精子获能过程中不同的翻译现象。
我们发现精子相关蛋白(SPACA)1和SPACA5在正常生育力精子的头部新合成,而在生育力降低的精子中,头部缺乏新合成的蛋白质,并且SPACA1和SPACA5相对较早丢失。此外,线粒体翻译抑制剂氯霉素部分抑制精子翻译并延迟易位,表明线粒体参与精子翻译。
我们的结果揭示了获能过程中精子蛋白质组随时间顺序的微环境变化,这导致了完成受精的蛋白质的协同作用。在雌性生殖道受精过程中,通过相互竞争选择出有生育能力的精子。本研究概述了翻译动力学如何作用于精子选择并影响精子生育力的演变。