Abstract
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 Gykl1 or Gk2 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.
Highlights
Mitochondria are sites of oxidative phosphorylation and essential for cellular energy production [1]
Patients with X-linked recessive glycerol kinase deficiency (GKD), which is caused by enzymatic inactivation or Gyk deletion [34], suffer from asymptomatic hyperglyceridaemia, growth and psychomotor retardation and metabolic disorders [25, 34, 35]
Unlike Gyk, which was detectable in the kidney and brain of C57BL/6J mice, glycerol kinase-like 1 (Gykl1) and glycerol kinase 2 (Gk2) mRNAs were found in mouse testis (Supplementary Figure S1B) [29, 33]
Summary
Mitochondria are sites of oxidative phosphorylation and essential for cellular energy production [1]. They change in shape and size and undergo fusion, fission, transport and mitophagy, which involve complicated steps and. While the exact mechanisms and physiological significance of mitochondria dynamics remain under active investigation, multiple players have been uncovered. Both mitochondrial fusion and fission appear to be mediated by mitochondrial membrane proteins and dynamin family members. Further investigations showed that the phosphatidate phosphatase LIPIN1 could terminate mitochondrial fusion by converting PA into DAG [16]. Phosphatidic acidpreferring phospholipase A1 (Pa-pla1) can deacylate PA into LPA, inhibiting mitochondrial fusion induced by Pld6 [1]
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