Spatiotemporal translation of sperm acrosome associated proteins during early capacitation modulates sperm fertilizing ability

IF 13 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Journal of Advanced Research Pub Date : 2026-01-01 Epub Date: 2025-03-18 DOI:10.1016/j.jare.2025.03.035
Yoo-Jin Park, Won-Ki Pang, Do-Yeal Ryu, Md Saidur Rahman, Myung-Geol Pang
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Abstract

Introduction

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.

Objectives

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.

Methods

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.

Results

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.

Conclusion

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.

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精子顶体相关蛋白在获能早期的时空翻译调节精子的受精能力
尽管成熟精子缺乏必要的细胞器,这为转录和翻译创造了不利的条件,但在获能过程中各种mRNA和蛋白质的存在表明有可能重新合成蛋白质。目的应用荧光非规范氨基酸标记系统(FUNCAT)和近端结扎法(PLA)对正常精子和低生育能力精子进行代谢标记,检测精子获能过程中不同的翻译现象。方法以正常[平均生育率(FR) = 77.44 %±1.51]和生育力降低(平均FR = 58.57 %±1.64)的公牛精子为代表的雄性生殖模式,由于其具有广泛的生育表型,我们根据时间顺序(0、20、40、60和120 min)对其蛋白质组变化进行了研究。此外,利用FUNCAT/PLA方法检测和可视化精子获能过程中不同的翻译现象。结果精子相关蛋白(SPACA1)和SPACA5在正常生育的精子头部有新合成,而在生育能力低下的精子头部缺乏新合成的蛋白,SPACA1和SPACA5的缺失相对较早。此外,线粒体翻译抑制剂氯霉素部分抑制精子翻译和延迟易位,表明线粒体参与了精子翻译。结论我们的研究结果揭示了精子获能过程中蛋白质组的微环境时序变化,这导致了完成受精的蛋白质群。可育精子是在雌性生殖道受精过程中通过相互竞争选择出来的。本研究概述了翻译动力学如何作用于精子选择和影响精子生育能力的进化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Advanced Research
Journal of Advanced Research Multidisciplinary-Multidisciplinary
CiteScore
21.60
自引率
0.90%
发文量
280
审稿时长
12 weeks
期刊介绍: Journal of Advanced Research (J. Adv. Res.) is an applied/natural sciences, peer-reviewed journal that focuses on interdisciplinary research. The journal aims to contribute to applied research and knowledge worldwide through the publication of original and high-quality research articles in the fields of Medicine, Pharmaceutical Sciences, Dentistry, Physical Therapy, Veterinary Medicine, and Basic and Biological Sciences. The following abstracting and indexing services cover the Journal of Advanced Research: PubMed/Medline, Essential Science Indicators, Web of Science, Scopus, PubMed Central, PubMed, Science Citation Index Expanded, Directory of Open Access Journals (DOAJ), and INSPEC.
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