Chen Yuxi, Liang Puping, Huang Yan, Li Minyan, Zhang Xiya, Ding Chenhui, Feng Junyan, Zhang Zhen, Zhang Xueqing, Gao Yuanzhu, Zhang Qinfeng, Cao Shanbo, Zheng Haiyan, Liu Dan, Songyang Zhou, Huang Junjiu
Key Laboratory of Gene Engineering of the Ministry of Education, Institute of Healthy Aging Research and State Key Laboratory of Biocontrol, SYSU-BCM Joint Research Center, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.
Cell Discov. 2017 Aug 22;3:17030. doi: 10.1038/celldisc.2017.30. eCollection 2017.
Spermatids undergo the final steps of maturation during spermiogenesis, a process that necessitates extensive rearrangement of organelles such as the mitochondria. Male infertility has been linked to mitochondrial disorder, for example, hypospermatogenesis and asthenozoospermia. However, the mechanisms that regulate mitochondrial dynamics during spermiogenesis remain largely unknown. We found the glycerol kinase (Gyk)-like proteins glycerol kinase-like 1 (Gykl1) and glycerol kinase 2 (Gk2) were specifically localized to the mitochondria in spermatids. Male mice deficient in either or were infertile due to dysfunctional spermatozoa, which exhibited unregulated ATP production, disordered mitochondrial sheath formation, abnormal mitochondrial morphology, and defective sperm tail. We demonstrated that the unique C-terminal sequences found in Gykl1 and Gk2 mediated their targeting to the mitochondrial outer membrane. Furthermore, both Gykl1 and Gk2 could interact with Pld6 (MitoPLD) and induce Pld6 and phosphatidic acid (PA)-dependent mitochondrial clustering in cells. Taken together, our study has revealed previously unsuspected functions of Gyk-like proteins in spermiogenesis, providing new insight into the potential mechanisms that lead to spermatozoa dysfunction and male infertility.
在精子形成过程中,精子细胞经历成熟的最后阶段,这一过程需要对线粒体等细胞器进行广泛的重新排列。男性不育与线粒体功能障碍有关,例如精子发生减少和弱精子症。然而,在精子形成过程中调节线粒体动态变化的机制在很大程度上仍然未知。我们发现,甘油激酶(Gyk)样蛋白甘油激酶样1(Gykl1)和甘油激酶2(Gk2)特异性定位于精子细胞的线粒体中。缺乏Gykl1或Gk2的雄性小鼠由于精子功能障碍而不育,这些精子表现出ATP产生不受调控、线粒体鞘形成紊乱、线粒体形态异常以及精子尾部缺陷。我们证明,在Gykl1和Gk2中发现的独特C末端序列介导了它们定位于线粒体外膜。此外,Gykl1和Gk2都可以与Pld6(线粒体磷脂酶D)相互作用,并在细胞中诱导Pld6和磷脂酸(PA)依赖性的线粒体聚集。综上所述,我们的研究揭示了Gyk样蛋白在精子形成过程中以前未被怀疑的功能,为导致精子功能障碍和男性不育的潜在机制提供了新的见解。