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小鼠精子发生的阶段解析磷酸化蛋白质组图谱揭示了精子形态发生中的关键激酶信号传导

Stage-Resolved Phosphoproteomic Landscape of Mouse Spermiogenesis Reveals Key Kinase Signaling in Sperm Morphogenesis.

作者信息

Zhu Tianyu, Zhu Yan, Jiang Xinyi, Zhang Xiangzheng, Wang Bing, Chen Yu, Zhao Yichen, Wang Yulian, Zhou Qi, Han Zhongyan, Qi Yaling, Luo Mengjiao, Tu Haixia, Hao Bingjie, Gao Mengmeng, Ren Jie, Zhou Xin, Zhang Xingyu, Chen Xu, Li Haojie, Huang Qian, Situ Chenghao, Guo Yueshuai, Zhu Hui, Li Yan, Guo Xuejiang

机构信息

State Key Laboratory of Reproductive Medicine and Offspring Health, Department of Histology and Embryology, Gusu School, Nanjing Medical University, Nanjing, 211166, China.

Department of Bioinformatics, Fujian Key Laboratory of Medical Bioinformatics, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, 350122, China.

出版信息

Adv Sci (Weinh). 2025 Sep 3:e08538. doi: 10.1002/advs.202508538.

Abstract

Spermiogenesis is the committed step of sperm production, during which spermatid cells undergo dramatic morphological transformations and transcriptional silencing. Post-translational modifications (PTMs), including phosphorylation, provide a level of protein function flexibility and play important roles in spermiogenesis. Dynamic protein phosphorylation profiles of spermatids are characterized across four different developing steps, and identified phosphorylation regulation of key proteins in spermiogenesis. Expression module and kinase-substrate phosphorylation network analysis revealed significant kinase activities of CSNK1G1 and TTBK2. CSNK1G1 is localized in the acrosome and is indispensable for acrosome biogenesis. Ttbk2 male germ cell conditional knockout mice are infertile with flagella development and head shaping defects. TTBK2 is essential for both the phosphorylation and stabilization of IFT88, an intraflagellar transport (IFT) protein with which TTBK2 colocalizes and interacts. Ciliogenesis defects in Ttbk2 knockout cells can be rescued by overexpression of TTBK2 or IFT88 but not kinase-dead TTBK2. Collectively, the systematic profiling of the spermiogenesis phosphoproteome revealed the dynamic nature and important functions of kinase phosphorylation in spermiogenesis and male fertility.

摘要

精子形成是精子产生的关键步骤,在此过程中,精子细胞经历了显著的形态转变和转录沉默。包括磷酸化在内的翻译后修饰(PTM)为蛋白质功能提供了一定程度的灵活性,并在精子形成中发挥重要作用。研究了精子在四个不同发育阶段的动态蛋白质磷酸化谱,并确定了精子形成过程中关键蛋白质的磷酸化调控。表达模块和激酶-底物磷酸化网络分析揭示了CSNK1G1和TTBK2的显著激酶活性。CSNK1G1定位于顶体,对顶体生物发生不可或缺。Ttbk2雄性生殖细胞条件性敲除小鼠不育,伴有鞭毛发育和头部形态缺陷。TTBK2对于IFT88的磷酸化和稳定至关重要,IFT88是一种鞭毛内运输(IFT)蛋白,与TTBK2共定位并相互作用。Ttbk2敲除细胞中的纤毛发生缺陷可通过过表达TTBK2或IFT88来挽救,但不能通过激酶失活的TTBK2来挽救。总的来说,精子形成磷酸化蛋白质组的系统分析揭示了激酶磷酸化在精子形成和雄性生育中的动态性质和重要功能。

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