Introduction

Spermiogenesis is the post-meiotic phase of male germ cell development during which the haploid spermatids differentiate into mature spermatozoa¹. Mouse spermiogenesis consists of 16 steps characterized by morphological changes in acrosome formation, nuclear condensation and elongation, flagellum formation, and cytoplasm removal². Acrosome biogenesis is one of the key events of spermiogenesis, and it begins with the initial stage of spermatid development. The acrosome is a specialized organelle with a cap-like structure covering the anterior part of the mature spermatozoon head and is indispensable for the fertilization process³. Although acrosome biogenesis is thought to be derived from the Golgi complex in early spermatids, growing evidence suggests that the endoplasmic reticulum (ER) and lysosomes are involved in acrosome biogenesis⁴. Defects in acrosome biogenesis can result in subfertility or infertility.

Acrosome biogenesis is generally classified into four successive phases, namely the Golgi, cap, acrosome, and maturation phases⁵. A number of ER and Golgi-associated proteins have been shown to be involved in acrosome biogenesis. Heat shock protein 90B1 (Hsp90b1) is an ER molecular chaperone that has been shown to be a testis-specific protein, and Hsp90b1 deficiency leads to a globozoospermia-syndrome like phenotype ⁶. Gm130 (Golgi matrix protein 130) localize on the cis surface of the Golgi apparatus, and loss of Gm130 causes acrosome malformations and results in male infertility⁷. Gopc (Golgi-associated PDZ and coiled-coil motif-containing) is a trans-Golgi-associated protein that plays a role in vesicle transport from the Golgi apparatus. Gopc deficiency leads to vesicle transport failure, which in turn results in malformation of the acrosome and to infertility⁸. Other vesicle transport proteins – including Pick1, Ica1l, and Vps13b – are involved in proacrosomal vesicle trafficking during acrosome formation^9,10. Recent evidence suggests that autophagy is involved in proacrosomal vesicle fusion and transport to form the acrosome, and disruption of Atg7^11,12 or Atg5 causes aberrant acrosome formation and male infertility or subfertility. Despite these findings, further studies are needed to better understand the complexity of acrosome biogenesis.

Transmembrane channel-like (Tmc) proteins are highly conserved ion channel-like proteins, with eight family members (Tmc1–Tmc8) identified in humans and mice ^13–16. Tmc proteins are predicted to have 6–10 transmembrane domains, and all protein members contain a conserved 120 amino acid Tmc domain¹⁵. The single-particle cryo-electron microscopy structure shows that Tmc1 assembles as dimers and that each monomer contains 10 transmembrane domains with four domains (S4–S7) that line the channel pore¹⁷. Tmc1 and 2 are mechano-electrical transducer (MET) channels in cochlear hair cells, and mutations in Tmc1/2 cause deafness in humans and mice¹⁸ by disrupting hair cell mechanoelectrical transduction, and Tmc gene therapy can restore auditory function and balance in mice^19,20. Germline mutations in Tmc6 and Tmc8 are associated with epidermodysplasia verruciformis, which leads to increased susceptibility to HPV infection ^14,15. Among the eight Tmc protein members, Tmc1 and Tmc2 are well studied due to their role in hearing conduction, and understanding the physiological and functional roles of other Tmc family members remains a major challenge.

In this study, we found that Tmc7 begins to be expressed in diplotene spermatocytes and that it is expressed at high levels in round spermatids in mouse testes. By generating Tmc7 conventional knockout mice (Tmc7^−/−), we demonstrate that Tmc7 deficiency leads to aberrant Golgi morphology and impaired fusion of Golgi-derived vesicles to the acrosome, thus resulting in male infertility with an oligo-astheno-teratozoospermia (OAT) phenotype. Our findings provide new insights into the physiological role of Tmc family members in spermiogenesis.

Results

Tmc7 expression is confined to the testis, and deletion of Tmc7 leads to male infertility

To explore the roles of Tmc family members during spermatogenesis, we analyzed the expression of Tmc1–Tmc8 using the mouse developmental transcriptome (E-MTAB-6798)²¹. Among the eight Tmc family proteins, we found that only Tmc5 and Tmc7 exhibited elevated expression in the testis during development (Fig. 1a). Tmc7 caught our great interest because Tmc7 was expressed at higher levels than Tmc5 in the testis during development. We next analyzed Tmc7 expression in different tissues using single-cell transcriptomic data from the Mouse Cell Atlas database²². We found that Tmc7 was predominantly expressed in the testis when compared with all other analyzed tissues (Fig. 1b). Further, we analyzed Tmc7 in different stages of germ cell development using single-cell sequencing data of male-specific tissues and organs in mice and humans²³. Interestingly, Tmc7 began to be expressed in diplotene spermatocytes and was expressed at high levels in round spermatids in mouse testes (Fig. 1c, d). The Tmc7 expression pattern was confirmed by RT-PCR (Fig. 1e, f), and Tmc7 was again found to be highly expressed in round spermatids of human testis (Fig. S1a, b). The distinct expression pattern in the testis indicates the potential role of Tmc7 in spermatogenesis.

Fig 1.

We generated Tmc7-deficient mice (Tmc7^−/−) by partial deletion of exon 2 (the first 241 bp) using the CRISPR/Cas9 system (Fig. 1g). Tmc7^−/− mice were confirmed by PCR-based genotyping and immunoblotting of the separated cytoplasmic and membrane testis proteins (Fig. S1c, d). We then examined the phenotypes and found that Tmc7-deficient mice were viable and had a normal appearance and exhibited a normal metabolic rate (Fig. S1e-j). However, Tmc7-deficient male mice showed smaller testes (Fig. 1h, i) and a reduced testis/body weight ratio (Fig. 1j) compared to control mice. Moreover, Tmc7^−/− male mice exhibited complete infertility (Table S1). No difference in the number of tubules per testicle or in the number of Sertoli cells was seen when comparing Tmc7^−/− and WT mice; Sertoli cell were identified by immunofluorescence staining of the Sertoli cell marker Sox9 (Fig. S1k, i). These findings suggest that Tmc7 is essential for spermatogenesis and thus for male fertility.

Tmc7 deficiency leads to severe defects in spermiogenesis

To determine the cause of infertility in Tmc7^−/− mice, we examined the composition of cell types in seminiferous tubules and cauda epididymis sections using hematoxylin staining in mouse testes at different developmental stages. In seminiferous tubules, the populations of germ cells were comparable between wild type (WT) and Tmc7^−/− mice at postnatal day (PD)14 and PD21. Intriguingly, the number of elongating spermatids in Tmc7^−/− mice decreased significantly compared with WT mice at PD28 (Fig. S2a). We next examined the testis and cauda epididymis sections of 9-week-old WT and Tmc7^−/− mice. We observed spermiogenesis defects in Tmc7^−/− mice as evidenced by the reduced number of elongating spermatids, the increased number of sloughed germ cells, and large vacuoles in the seminiferous tubules and cauda epididymis (Fig. 2a, b). The vacuolation became more serious with increasing age (Fig. S2a). The total number of sperm in the cauda epididymis was drastically decreased in Tmc7^−/− mice (∼0.15 × 10⁶ cells) compared to wild type (WT) mice (∼8.5 × 10⁶ cells) (Fig. 2c). The morphological assessment of spermatozoa from the caudal epididymis revealed that a large proportion of spermatozoa (∼85%) in Tmc7^−/− mice exhibited abnormal head morphology, similar to human OAT (Fig. 2d, e). In parallel with this, periodic acid Schiff (PAS) staining indicated that a large number of spermatids failed to differentiate into elongated spermatids with sickle-shaped heads and instead exhibited abnormal head morphology. The total number of spermatids began to significantly decrease at steps 9–12 of spermiogenesis (Fig. 2f, g), and we performed Mito-tracker staining and found shortened or disorganized mitochondrial sheaths in Tmc7^−/− spermatozoa collected from the cauda epididymis (Fig. 2h). Meanwhile, no motile or progressive sperm were found in the Tmc7^−/− mice (Fig. 2i, j). Moreover, meiotic progression was not affected in Tmc7^−/− mice as evidenced by immunofluorescence staining of the meiosis markers Sycp3 (red) and γH2ax (green) in the seminiferous tubules of PD20 WT and Tmc7^−/− mice (Fig. S3a). Overall, we concluded that Tmc7 ablation results in defects in spermiogenesis and in OAT-like phenotypes.

Fig 2.

Acrosome biogenesis is impaired starting from the Golgi phase in Tmc7^−/− spermatids

Acrosome biogenesis is one of the key events of spermiogenesis. To investigate whether Tmc7 is required for the proper formation of the acrosome, FITC-labelled peanut agglutinin (PNA) was used to assess the acrosomal status of spermatids in 9-week-old WT and Tmc7^−/− mice. The spermatids of WT mice had normal structures in the Golgi, cap, acrosome, and maturation phases, while spermatids in Tmc7^−/− mice exhibited abnormal acrosome morphology as early as the Golgi phase. Fragmented and malformed acrosomes were observed in all four phases of spermatids in the Tmc7^−/− mice (Fig. 3a). Absent or fragmented acrosomes were also found in Tmc7^−/− spermatids collected from the cauda epididymis (Fig. S4a). To better understand the morphologic defects of the acrosome in greater detail, transmission electron microscopy (TEM) was performed to analyze the acrosome structure in WT and Tmc7^−/− mice. We found that large vesicles accumulated adjacent to developing acrosomes in all phases of acrosome biogenesis, starting from the Golgi phase (Fig. 3b, left panel) in the spermatids of Tmc7^−/− mice. Additionally, abnormal acrosome structures and defective nuclear condensation were observed in Tmc7^−/− spermatids (Fig. 3b, right panels). Further investigation revealed that knockout of Tmc7 resulted in Golgi apparatus fragmentation and disorganization, as determined by TEM and immunofluorescence staining of the Golgi marker Gm130 (Fig. 3b-c). The aspect ratio (height over width) of the Golgi apparatuses in Tmc7^−/−spermatids (R = ∼2.9) based on TEM images were also significantly smaller than in WT spermatids (R = ∼4.9) (Fig. 3d). Meanwhile, we found that the Golgi body failed to correctly orient toward the acrosome (Fig. S4b). We further performed immunoblotting to measure Golgi stress markers, Hsp47 and Tfe3 in 9-week-old Tmc7^−/− testes compared with WT testes. The results showed that the protein levels of Hsp47 and Tfe3 were significantly increased upon loss of Tmc7, indicating the occurrence of Golgi stress (Fig. 3e). Gopc is localized in the trans-Golgi network and is involved in the transport and fusion of the proacrosomal vesicles with the acrosome⁸. By immunostaining for Gopc and PNA, we found that Gopc staining (red) was colocalized with PNA (green) in WT spermatids. In contrast, colocalized Gopc and PNA spermatids were significantly decreased in Tmc7^−/− mice (Fig. 3f). Together these findings suggest that Tmc7 is required for proacrosomal vesicle trafficking and fusion during acrosome biogenesis.

Figure 3.

Tmc7 localizes to the cis-Golgi, and this is required for maintaining Golgi integrity

To further delineate the role of Tmc7 in acrosome formation, we next sought to determine the subcellular localization of Tmc7 in the testis. We performed immunostaining and found that Tmc7 was predominantly expressed in the perinuclear regions of pachytene spermatocytes and round spermatids in WT testes but not in Tmc7^−/− testes, suggesting the specificity of the antibody (Fig. 4a). By immunofluorescence co-staining of Tmc7 with the cis-Golgi marker Gm130, the trans-Golgi marker Tgn46, and PNA, we found that Tmc7 colocalized closely with Gm130 but not with Tgn46 (Fig. 4b, c, Fig. S5a), indicating its localization to the cis-Golgi apparatus. Further evaluation showed that Tmc7 and PNA were closely associated but not colocalized (Fig. 4d, Fig. S5b). In parallel, we carried out co-immunoprecipitation with Tmc7 antibody coupled with immunoblotting in mouse testes and found that Tmc7 was able to pull down Gm130, the Gm130-interacting protein P115, and Grasp65 (Fig. 4e), further confirming that Tmc7 is localized to the cis-Golgi apparatus.

Figure 4.

Gm130 is reported to be involved in maintaining the function and integrity of the Golgi apparatus⁷. To gain more insight into the role of Tmc7 in the Golgi apparatus, we performed immunostaining against Gm130, P115, and Grasp65 in the testes of 9-week-old WT and Tmc7^−/− mice. The results showed that the protein levels of Gm130, P115, and Grasp65 were significantly reduced in Tmc7^−/− testes compared to WT testes (Fig. 4f, g, Fig. S5c-e). Immunoblotting further verified the reduced levels of Gm130, P115, and Grasp65 upon loss of Tmc7 (Fig. 4h). These results suggest that Tmc7 colocalizes to Gm30 in the cis-Golgi and that this is required for maintaining Golgi integrity.

Tmc7 depletion impairs cellular homeostasis and leads to spermatid apoptosis

Golgi pH and ion homeostasis is essential for proper function, including membrane trafficking, protein glycosylation, and protein sorting²⁴, and the Golgi apparatus has been shown to be another intracellular Ca²⁺ store in addition to the endoplasmic reticulum (ER)²⁵. Tmc1 mutation leads to reduced Ca²⁺ permeability, thus triggering hair cell apoptosis and subsequent deafness²⁶. We measured intracellular Ca²⁺ by flow cytometry in WT and Tmc7^−/− germ cells isolated from PD30 testes. The results showed that the intracellular Ca²⁺ concentration was significantly reduced in Tmc7^−/− germ cells compared to WT germ cells (Fig. 5a). In contrast, intracellular pH was increased in Tmc7^−/− germ cells compared to WT germ cells (Fig. 5b). These results suggest that the pH and ion homeostasis was impaired. We further measured the reactive oxygen species (ROS) levels and observed that ROS levels were significantly increased upon loss of Tmc7 (Fig. 5c) In addition, we examined ER stress-related proteins by immunoblotting and found that p-eif2α, Chop, and Grp78 were significantly increased in 9-week-old Tmc7^−/− testes compared with WT testes, indicating the occurrence of ER stress (Fig. 5d). Moreover, we carried out TUNEL staining in the seminiferous tubules and cauda epididymis of 9-week-old WT and Tmc7^−/− mice. The TUNEL-positive cells in seminiferous tubules and cauda epididymis were significantly increased in Tmc7^−/− mice compare to WT mice (Fig. 5e). The expression of apoptosis-related proteins was next measured by immunoblotting, and depletion of Tmc7 increased the levels of cleaved caspase-3 and Bax and decreased the levels of Bcl2 (Fig. 5f). These results support the hypothesis that Tmc7 is required to maintain Golgi pH and ion homeostasis and that this is needed for acrosome biogenesis.

Fig 5.

Discussion

Among the eight Tmc protein members, Tmc1 and Tmc2 are localized to the site of MET channels at the tips of the shorter stereocilia of cochlear hair cells^27,28, and mutations in Tmc1 and Tmc2 cause deafness. However, Tmc1 and Tmc2 expressed in heterologous cell lines remain in the ER and fail to localize to the plasma membrane¹⁸. Tmc4 is a voltage-dependent chloride channel that is predominantly expressed in the taste buds in the posterior region of the tongue²⁹. Tmc6 and Tmc8 are localized to the ER and play crucial roles in zinc transport³⁰. However, the physiological function of Tmc7 has not been defined. In this study, we demonstrated that Tmc7 was predominantly expressed in testes (Fig. 1e), and by generating knockout mice lacking Tmc7 we found that Tmc7 deficiency resulted in complete male infertility with an OAT-like phenotype. Interestingly, we found that Tmc7 co-localized with Gm130, but not with Tgn46 (Fig. 4b, c), as illustrated by the immunofluorescence co-staining assay, indicating that Tmc7 located on the cis side of the Golgi apparatus.

Our results demonstrate the critical role of Tmc7 during the formation of the acrosome. The acrosome is thought to be derived from the Golgi apparatus, so we speculated that Tmc7 deficiency might cause defects in acrosome formation because Tmc7 localized on the Golgi apparatus. We observed fragmented and malformed acrosomes starting from the Golgi phase in Tmc7^−/− spermatids as analyzed by TEM (Fig. 3b). Additionally, proacrosomal vesicles were found to accumulate around the acrosomes (Fig. 3b), and spermatids with colocalized Gopc and PNA were significantly decreased in Tmc7^−/− mice (Fig. 3f), suggesting that Golgi-derived vesicles failed to fuse with developing acrosomes. In accordance with our findings, other proteins that localize on the Golgi apparatus have also been reported to be involved in acrosome biogenesis. Gm130 deficiency results in acrosome biogenesis failure and male infertility because proacrosomal vesicles are unable to fuse to form acrosomes³⁰. Our findings showed that Tmc7 was co-localized with Gm130 and that Tmc7 depletion significantly reduced the protein level of Gm130. Gopc is localized on the trans-Golgi region, and its deficiency leads to defective fusion of Golgi-derived transport vesicles to the acrosomal cap and to a complete lack of acrosomes⁸. Colocalized Gopc and PNA spermatids were significantly decreased in Tmc7^−/− spermatids compared to WT spermatids. Further, Golga3, Pick1, and several other Golgi proteins are also required for acrosome biogenesis³¹. Our work, combined with previous studies, broadens our understanding of role the Golgi apparatus plays in the formation of acrosomes.

Our findings highlight the role of Tmc7 in maintaining Golgi and cellular homeostasis. Upon Tmc7 depletion, the Golgi apparatus undergoes significant disorganization and is unable to correctly orient toward the acrosome. The mechanism behind this is that intracellular Ca²⁺ concentrations decreased while the pH value was increased in Tmc7^−/− germ cells compared to WT germ cells, suggesting that Tmc7 is essential for maintaining the pH and ion homeostasis of the Golgi apparatus. Our findings further revealed that Tmc7 deficiency led to increased ROS levels, Golgi and ER stress, ultimately resulting in apoptosis of spermatids. The Na⁺/H⁺ exchanger Nhe8 is involved in the maintenance of intracellular pH and ion homeostasis, and Nhe8 deficiency leads to Golgi-derived vesicles failing to form large acrosomal granules and the acrosomal cap³². Slc9a3 is another Na⁺/H⁺ exchanger, and it is expressed in the acrosomal region of spermatids and loss of Slc9a3 causes severe acrosomal defects³³. These studies, together with our current findings, support the hypothesis that pH and ion homeostasis of the Golgi apparatus is needed for the proper progression of acrosome biogenesis.

In conclusion, our findings show that Tmc7 localizes to the cis-Golgi region in spermatids and that this is essential for acrosome biogenesis and for male fertility. In the absence of Tmc7, Golgi pH and ion homeostasis is disrupted, and this leads to Golgi disorganization and failure to correctly orientate to the acrosome. Subsequently, Golgi-derived proacrosomal vesicles are unable to fuse with the developing acrosome and acrosome biogenesis is severely impaired, and thus Tmc7-deficent male mice are completely infertile. Our study highlights the physiological role of TMC family members in spermatogenesis.

Materials and methods

Generation of Tmc7 knockout mice

Tmc7 conventional knockout mice in the C57BL/6J background were obtained from Cyagen Bioscience (China). Exon 2 was selected as the target site, and Cas9 mRNA and single guide RNA were co-injected into fertilized eggs for knockout mouse production. The pups were genotyped by PCR using the following primers: F1:5’-AGA TGG CTT AGT GGG TGC CTT AGT-3’; R1:5’TGA TGG ACA GAG AGA TGA TGA ATG G-3’; F3: 5’-CAG TCC CAG GTT CAG TTC AGT GAG-3’. In WT mice, the primer pair amplified a 513 bp PCR product, while in Tmc7^−/− mice it amplified an 891 bp product. Mice were housed under a controlled illumination regime (light for 12 h) at 21°C–22°C and 60% ± 10% relative humidity. Food and water were freely available, and all animal experiments were conducted in accordance with the guidelines of the Animal Care and Use Committee at Shandong University (ECSBMSSDU2022-2-113).

Metabolic assessment in mice

A Columbus Instruments Comprehensive Lab Animal Monitoring System CLAMS6 was used for the experiment. Nine-week-old WT and Tmc7^−/− male mice (n = 4) were weighed and had the metabolic rates measured over a period of 48 hours. The rate of oxygen consumption, RER (breathing entropy), energy expenditure, and food intake were automatically recorded every eight minutes. These data were analyzed with a 12 h dark:12 h light cycle at 22–23 °C.

RNA isolation and PCR

The tissues were homogenized in TRIzol (Invitrogen, 15596-026) with a grinder. Following centrifugation, the RNA in the supernatant was obtained by precipitating with isopropanol and washing with ethanol. A total of 1 μg RNA was reverse-transcribed into cDNA with HiScript III RT SuperMix for RT-PCR (+gDNA wiper) (Vazyme, R223-01) according to the manufacturer’s instructions. The cDNA was used to detect the expression of Tmc7 with Taq Master Mix (Vazyme, P112-03) with the following primers: F – AGC CAA TCC ATC CGC AAG TAT; R – TGC TGC TG TAC CGT TTC CAC. The products were analyzed by agarose gel electrophoresis.

Sperm collection

The cauda epididymis was collected and placed in an EP tube containing PBS. Sperm were released for 30 min in an atmosphere of 5% CO₂ at 37 °C. The suspension was diluted at 1:50 and transferred to a hemocytometer for counting. For the anther experiments, the PBS with sperm was spread on the slide and fixed with 4% paraformaldehyde (Servicebio, G1101). The slides were stored at –80°C after drying.

Histological analysis

For the morphology analysis of the sperm from the caudal epididymis, sperm smears were directly stained with hematoxylin and sealed with neutral balsam. The tissue was fixed in 4% paraformaldehyde overnight, then dehydrated and embedded in paraffin. Paraffin-embedded tissues were sectioned at 4 μm. Tissue slides were deparaffinized in xylene and dehydrated in a series of ethanol. The tissues were then stained by hematoxylin or with periodic acid staining using a PAS Stain Kit (Abcam, ab150680) according to the manufacturer’s instructions. Finally, tissue slides were rehydrated in a series of ethanol and xylene and sealed with neutral balsam. An Olympus BX53 microscope system was used for imaging.

Immunofluorescence

We performed immunofluorescence of germ cells in the testes using two methods, including testis slides and squashed seminiferous tubules. The squashed seminiferous tubules were prepared according to a previous report³⁴. The testis slides were deparaffinized in xylene and rehydrated in a series of ethanol. Antigen retrieval was performed by heating in EDTA Antigen Retrieval Solution (pH 9.0) (ZSGB-BIO, ZLI-9096), and nonspecific binding sites were blocked with EZ-Buffers M 1X Block BSA in PBS (Sangon, C520035-0250). The slides were incubated with primary antibody overnight at 4℃. Primary antibodies included anti-Tmc7 (1:200 dilution, Abcam, ab191521), anti-Sox9 (1:500 dilution, Sigma, AB5535), anti-Gopc (1:200 dilution, Proteintech, 12163-1-AP), anti-Sycp3 (1:500 dilution, Santa Cruz, sc-33195), anti-H2ax (1:500 dilution, Millipore, 05-636-1), anti-Gm130 (1:100 dilution, 610822, BD Biosciences), anti-P115 (1:200 dilution, Proteintech, 13509-1-AP), and anti-Grasp65 (1:200 dilution, Proteintech, 10747-2-AP). The next day they were incubated with the secondary antibody (1:500 dilution, Thermo, A-11070 and A-11012) for 1 h at room temperature. The Alexa Fluor 488 conjugates of lectin PNA (1:500 dilution, Thermo, L21409), anti-Gm130 (1:200 dilution, Proteintech, CL488-11308), and anti-Tgn46 (1:200 dilution, Proteintech, CL488-13573) were used as secondary antibodies. For the staining of Mito-track (1:5000 dilution, Beyotime, C1048), the sperm released from the caudal epididymis were directly stained for 30 min at 37 °C. The sperm were then spread on the slide and observed. A TUNEL assay was performed using a one-step TUNEL Apoptosis Assay Kit (KeyGEN BioTECH, KGA7072) according to the manufacturer’s instructions. Briefly, the slide was deparaffinized and antigen retrieval was performed. dUTP was used to label the cells, and the nuclei were stained with DAPI (Abcam, ab285390). Fluorescent images were captured on a Dragonfly 200 confocal microscopy system (Andor Technology).

Western blotting

The membrane and cytoplasmic proteins of the testis were obtained using a membrane protein extraction kit (Abmart, A1008) according to the manufacturer’s instructions. Total protein in the testis was obtained by grinding in a tissue grinder in RIPA lysis buffer (Beyotime, P0013B), and the concentration of protein was measured using a BCA protein assay kit (Beyotime, P0009). The proteins were separated by SDS-PAGE and then transferred to a PVDF membrane. The membranes were blocked in 5 % non-fat milk and then incubated with primary antibodies overnight at 4 °C. Primary antibodies included anti-Tmc7 (Dia-an Biotech), anti-Atp1a1 (Proteintech, 14418-1-AP), anti-Gapdh (Proteintech, 60004-1-1g), anti-Cleaved-Caspase3 (Cell Signaling Technology, 9661), anti-Caspase3 (Cell Signaling Technology, 9662), anti-Bax (Cell Signaling Technology, 41162), anti-Bcl2 (Cell Signaling Technology, 17447), anti-α-Tubulin (Proteintech,11224-1-AP), anti-P-Eif2α (ABclonal, AP0745), anti-Eif2α (ABclonal, A0764), anti-Grp78 (Proteintech, 11587-1-AP), anti-Chop (Proteintech, 15204-1-AP), anti-P115 (Proteintech, 13509-1-AP), and anti-Grasp65 (Proteintech, 10747-2-AP). All antibodies were diluted 1:1000. The next day, the membrane was incubated with horseradish peroxidase-conjugated secondary antibody for 1 hour, and the protein was detected using an ECL system (Vazyme, E412-02). The quantitation was performed in Image J.

Chromosome spreading

Meiotic nuclear spreading was performed as previously reported³⁵. Briefly, spermatocytes released from seminiferous tubules were incubated in hypotonic solution for 1 hour and then transferred to 100 mM sucrose. The suspension was spread on the glass slides with 1% PFA and 0.15% Triton X100, and dried slides were stored at –80°C or were used for the immunofluorescence staining.

Transmission electron microscopy

The testes of 9-week-old WT and Tmc7^−/− mice (n = 3) were used for the TEM analysis. The testes were washed in PBS three times and then fixed in 1% O_SO₄ in 0.1 M PBS (pH 7.4) buffer at 4°C overnight. The testes were then fixed in 1% O_SO₄ at room temperature for 1 hour. The samples were then washed with water three times for 15 min each and dehydrated in a graded ethanol series (50%, 70%, 95%, and 100%). The samples were finally embedded with resin, cut into 80 nm sections, and viewed with a JEM-1400 transmission electron microscope.

Flow cytometry

The testes of PD30 WT and Tmc7^−/− mice (n = 3) were used to obtain germ cells. The tunica albuginea was removed and placed into PBS with 120 U/ml Type I Collagenase (Gibco, 17100-017) on a shaker at 37°C and 220 rpm for 10 min. The supernatant was filtered through a 70 μm cell filter screen into a new tube. The sediment was digested again with 0.25% trypsin-EDTA (Gibco, 25200–072) on a shaker at 37°C and 220 rpm for 10 min and then neutralized by serum albumin and filtered. The germ cells were obtained by centrifuging twice at 1000 × g for 5 min and then removing the supernatant.

The levels of Ca²⁺, pH, and ROS were measured using fluorescent probes according to the manufacturer’s protocols (Beyotime, S1056, S1006, S0033S). The probes were all diluted 1:2000. Germ cells were stained with the probes at 37°C for 30 min, then washed with PBS three times and analyzed by flow cytometry (Gallios, US).

Co-immunoprecipitation

Testes of 9-week-old WT mice were ground in a tissue grinder in RIPA Lysis Buffer (Beyotime, P0013B) to obtain the total protein. Tmc7 (Dia-an Biotech) and IgG (Beyotime, A7016) antibodies were incubated with the proteins overnight. The next day, they were incubated with protein A/G magnetic beads (MCE, HY-K0202) for 2 hours. The beads were wash and boiled for 10 min in 1× SDS loading buffer. Western blotting was used for the analysis of input and immunoprecipitated samples with anti-P115 and anti-Grasp65 antibodies.

Statistical analysis

GraphPad Prism 9 was used to analyze the data, and the results are shown as the mean ± standard deviation (S.D.). Statistical significance was determined using two-sided Student’s t-tests or two-way analysis of variance (ANOVA). *p < 0.05, **p < 0.01, and ***p < 0.001 indicate the level of statistical significance, and ns stands for not significant.

Acknowledgements

We thank Translational Medicine Core Facility of Shandong University for consultation and instrument availability that supported this work. We also thank the Laboratory Animal Center of Shandong University for mouse housing and care. This work was supported by National Natural Science Foundation of China (82172718, 82301801, 82303055, 81972437).

Author Contributions

J.W., Y.Y, performed most experiments, and data analysis, and writing the manuscript. Z.W., L.Y., performed public database sequence data analysis. C.Q., Y.G., L.Y., helped with animal and cell experiment. F.G., G.Lu., Z.C., X.Z., is involved technical, material support and guided the experiment. H.L., Z.L. Supervised the project and revised the manuscript. Zhaojian Liu was the lead contact for the study. Final approval: All authors.

Conflict of interest

The authors declare no competing interests.