The N-myc downstream regulated gene (NDRG) family consists of 4 members, NDRG-1, -2, -3, -4. Physiologically, we found Ndrg3, a critical gene which led to homologous lethality in the early embryo development, regulated the male meiosis in mouse. The expression of Ndrg3 was enhanced specifically in germ cells, and reached its peak level in the pachytene stage spermatocyte. Haplo-insufficiency of Ndrg3 gene led to sub-infertility during the male early maturation. In the Ndrg3+/− germ cells, some meiosis events such as DSB repair and synaptonemal complex formation were impaired. Disturbances on meiotic prophase progression and spermatogenesis were observed. In mechanism, the attenuation of pERK1/2 signaling was detected in the heterozygous testis. With our primary spermatocyte culture system, we found that lactate promoted DSB repair via ERK1/2 signaling in the male mouse germ cells in vitro. Deficiency of Ndrg3 gene attenuated the activation of ERK which further led to the aberrancy of DSB repair in the male germ cells in mouse. Taken together, we reported that Ndrg3 gene modulated the lactate induced ERK pathway to facilitate DSB repair in male germ cells, which further regulated meiosis and subsequently fertility in male mouse.
Spermatogenesis, by which the spermatogonia develop into highly specialized cells, spermatozoa, is the most essential and complex process in male reproduction1. Abnormal alterations of the events such as DSB repair and energy metabolism et al. in germ cells are potentially involved in hypo-spermatogenesis or even lead to ultimately male infertility2,3,4.
The programmed induction of the DSBs during meiosis allows the exchange of genetic material between homologous chromosomes which increases the genome diversity5,6,7. However, the DSBs are highly lethal lesions that jeopardize genome integrity8. Two major strategies, homologous recombination (HR) and non-homologous end joining (NHEJ) are used to control the DSB repair tightly9,10,11,12. DSBs provoke an extensive reaction in neighboring chromatin involving the covalent modifications of histones. Phosphorylation of the histone H2AX on serine 139 of its C-terminal tail (γH2AX) is used as a biomarker for cellular response to DSBs13,14,15. The γH2AX/MDC1 signaling pathway participates into both the HR and NHEJ DNA repair pathways16,17. Defects in DSB repair causes abnormal recombination and arrest of spermatogenesis, which ultimately result in male infertility18.
Testis, a tightly compartmentalized organ, is a place where the male germ cell matures. A metabolic profile shift from aerobic to anaerobic pathways in germ cells takes place as the differentiation of the male germ cells from spermatogonia to spermatozoa4. The metabolite lactate secreted from the sertoli cells is utilized as the central fuel for ATP producing during the male meiosis3,4,19,20. Latest reports showed that lactate could activate Raf-ERK signaling by binding to NDRG3 to mediate the lactate triggered hypoxia responses21,22.
Ndrg3 belongs to the N-myc down-regulated gene (NDRG) family23,24. Previous reports have suggested the involvement of the NDRG family in the early life development such as organ formation25,26,27,28, somite differentiation29. The multiple expression of NDRG3 in human tissues and organs, with the highest expression in testis23,30 is suggesting the presence of some important function of NDRG3 physiologically, especially in testis. The 5α-dihydrotestosterone regulated Ndrg3 at the beginning of spermatogenesis further implied the function of Ndrg3 gene may possibly be involved in spermatogenesis31. To date, however, little is known about the exact role of NDRG3 involved in such process.
In this study, we detected the temporo-spatial expression pattern of Ndrg3. It was tightly associated with meiosis progression in testis. Our genetically modified mouse model showed the haplo-insufficiency of Ndrg3 gene impaired the meiosis in the male germ cells, indicating the biological role of Ndrg3 in spermatogenesis. Our approach based on the in vitro primary germ cell culture further showed that Ndrg3 was required for the lactate induced DSB repair via modulating the ERK1/2 pathway. This study will also be helpful for providing a new prospect that how metabolite lactate influences meiosis in the male germ cells.
The Ndrg3 expression and distribution in testis
Given the highest expression of human NDRG3 existing in testis, we examined the distribution of Ndrg3 in mouse tissues by real-time PCR assay30. The mRNA level of Ndrg3 was detected highest in testis compared with other tissues (Fig. 1a). To further investigate the protein level of NDRG3 in testis, we analyzed its expression in the indicated ages. Western blot assay showed that the basal protein level of NDRG3 in testis was very low at 6 days postpartum (dpp), but strikingly induced at 12 dpp and 18 dpp significantly. An even higher expression level of NDRG3 was detected at 36 dpp (Fig. 1b). These data showed that the NDRG3 protein level was raised during the sexual maturation in male mice. To further identify the cell types in which NDRG3 was mainly expressed, the immunohistochemistry assay was carried out. The results showed that NDRG3 protein was detected specifically in germ cells including spermatogonia (green arrows), spermatocytes (red arrows) and spermatids (blue arrows) at 12–36 dpp (Fig. 1c), indicating that the Ndrg3 gene functioned in the male germ cell development during the spermatogenesis. We further compared the mRNA and protein levels of NDRG3 in spermatogonia, meiosis I prophase subgroups (leptotene, zygotene and pachytene & diplotene stages), spermatids and sertoli cells. Both of the results showed the expression of NDRG3 was exclusively in germ cells and largely induced in the meiosis I prophase spermatocytes and spermatids compared with the spermatogonium group. (Fig. 1d and e), implying that NDRG3 exerted the physiological role shortly after the initiation of the meiosis.
Establishment of NDRG3 deficient mice
To determine the role of Ndrg3 gene during spermatogenesis, we generated the C57BL/6 mice in which the Ndrg3 gene was disrupted by TALENs. In short, the TALENs were constructed to target the DNA sequence of the mouse Ndrg3 gene (Fig. 2a) as illustrated graphically in Fig. 2b. A 593 bp PCR product was amplified from each offspring and subjected to the endonuclease survey (T7E1), which cleaved the PCR amplicon into ~380-bp and ~210-bp fragments. Agarose gel photograph of the surveyor nuclease assay demonstrated the digestion products of predicted size from pup #2, #3, #5, #7, #8 with a ~380-bp and a ~210-bp fragments (Fig. 2c). The above chimeric offspring strains were then subjected to the DNA sequencing and one of the strains (#2) that 7-base deletion in the space area (caggatgttcaactcac) was detected (Fig. 2d). The strain #2 chimeric offspring were crossed to the C57BL/6 background wild type mouse to obtain the heterozygous mice. The heterozygous offspring were further confirmed by sequencing (Fig. 2e). However, we failed to obtain the Ndrg3−/− homology (Fig. 2f and g). The number of the pups with indicated genotypes was counted. The mean number of the wild type or heterozygous group was 16 or 31 respectively, indicating the homologous lethality effect of Ndrg3 (Fig. 2g). We examined the genotype of the embryos from E5.5 to the new born pups, but no homologous mouse was found (data not shown). Thus we thought NDRG3 may influence the early embryo development. We performed the neutralization experiment with an anti-NDRG3 antibody and control IgG in the one-cell stage fertilized eggs. As was shown, about 17.6% eggs developed to the blastocyst stage in the antibody treated group, whereas more than 60% eggs developed to that stage in the IgG treated group (Fig. 2h). The neutralization assay here helped to provide a piece of evidence that NDRG3 protein was required during the early embryo development. Western blot of the whole testis lysates from adult mouse testes showed that the Ndrg3 gene was disturbed in heterozygous resulted in a down regulated NDRG3 protein level (Fig. 2i).
Haplo-insufficiency of Ndrg3 impaired the fertility, testis development and spermatogenesis in male mice
Ndrg3+/− male mice were apparently normal in growth (data not shown). To investigate whether the fertility of Ndrg3+/− male was impaired, 5- to 8-week-old male heterozygous mice and their wild type littermates were mated with wild type (C57BL6) females (6-week-old) respectively. The number of average pups per Ndrg3+/− mouse was significantly decreased, when compared with the wild type litter mates at the indicated time points. The mean number of litters produced by wild type male was about 5.5 at 6-week period whereas the number of Ndrg3+/− group was 2.7. The number of the offspring produced by wild type male was 6 whereas the Ndrg3+/− group was 3.4 at 7-week period. The wild type group number was about 6.7 while the Ndrg3+/− group was 5.2 at 8-week period (Fig. 3a). The number of spermatozoa was significantly lower in Ndrg3+/− mice when compared with that in the wild type groups (Fig. 3b) at the time points of 6 to 8 weeks postpartum. The decreased numbers of pups and spermatozoa in the heterozygotes suggested that the deficiency of NDRG3 led to the sub-fertility during the early stage of male maturation. We examined the testis weight of the Ndrg3+/− and wild type groups from 6 to 48 dpp. Ndrg3+/− and wild type groups showed no apparent difference at 6 and 11 dpp. As the growth continuing, the mean weight number of Ndrg3+/− group was16, 20.5, 36 and 58.6 milligram at each time point respectively, which were significantly lower than that observed in the wild type group (Fig. 3c). On the other hand, we did not detect any significant difference in body weight (data not shown) between the two groups. Next, we performed histological analysis between the two group testes at early developmental stages in order to investigate the reasons causing subfertility and reduced testis weight in Ndrg3+/− mice. No obvious difference was observed between the wild type and Ndrg3+/− testis histology before 8 dpp (data not shown). At 18 dpp, we observed a large number of late pachytene spermatocytes in the wild type tubules whereas the most frequent spermatocytes presented was leptotene or zygotene-like stage cells in the Ndrg3+/− testes (Fig. 3d and e). As the Ndrg3 gene was high in brain (Fig. 1a), we also determined the testosterone level between the wild type and the Ndrg3+/− group, but no significantly changes were found (Supplemental Figure 1), indicating that the testicular tubule defect was mainly due to the development failure of the male germ cells. These above visible defects in spermatocyte development implied the abnormality of meiosis in the Ndrg3+/− testes. Taken together, haplo-insufficiency of Ndrg3 in testis impaired the male fertility, testis maturation, male germ cell development and spermatogenesis.
Deficiency of Ndrg3 resulted to the meiosis abnormality
According to the location of NDRG3 protein in tubules (Fig. 1) and the physiological defect found in testis (Fig. 3), we hypothesized that haplo-insufficiency of Ndrg3 affected meiosis in male. Firstly, the spermatogenesis progression analysis was performed using 8 weeks old mice. The morphologies of mid-pachytene spermatocyte, metaphase stage of spermatogonium, metaphase I and metaphase II spermatocyte were distinguished according to the previous study32 and the results were shown in Supplemental Figure 2. Based on counting the specific cell number per 1000 spermatocytes, Ndrg3+/− mouse resulted in a significant decrease in the frequencies of meiosis I metaphase (MMI) or meiosis II metaphase (MMII) (Table 1), indicating that spermatogenesis was disturbed in Ndrg3+/− mice. Secondly, we performed real-time PCR assay to find out which stage of spermatogenesis was affected. As was shown in Fig. 4a, no significant difference in the mRNA levels of Uchl1 and Gfra1 was found between the wild type and Ndrg3+/− testes (The expression of Uchl1 and Gfra1 is high in spermatogonia33,34), suggesting NDRG3 deficiency did not affect the spermatogonia. However, the mRNA levels of Sycp3, Sycp1 (synaptonemal complex (SC) proteins establishing the architecture of the meiotic chromosomes), Rec8 (a cohesion protein that binds sister chromatids together to form the synaptonemal complex35), Rad51, Dmc1, Mre11, Rad50 (DSB repair associated), Fzr1 (meiosis arrest associated) were found to be down-regulated significantly in the Ndrg3+/− testis. These results strongly suggested that the deficiency of Ndrg3 impaired the events appearing in the early stage of meiosis.
In order to further characterize the function of NDRG3 in the meiotic prophase I progression. Testicular cells were spread and stained with the anti-SYCP3 antibody, and the numbers of the germ cells in the indicated sub-stages of meiotic prophase I were counted, respectively. The relative ratios of the leptotene and zygotene stage cell of Ndrg3+/− mice were increased significantly compared with the wild type group (~16% vs ~11%, ~30% vs ~7% respectively), while the relative ratios of pachytene and diplotene stage cells were decreased in Ndrg3+/− mice (~45% vs ~64%, ~9% vs ~18% respectively) (Fig. 4b). This indicated that Ndrg3 deficiency interfered with the transition from zygotene to pachytene in male germ cells.
Dynamic changes in chromatin structure take place along the meiotic process accompanied by the histone H2AX phosphorylation at ser139 (γH2AX) which is triggered by the DNA double strand breaks (DSBs) formation. The phosphorylation of H2AX is detected on large domains of chromatin in the vicinity of the breaks13,14,15. After entering into the meiosis, the γH2AX signal is detected throughout the nuclei from the leptotene stage to the early zygotene stage. As meiosis proceeds to the pachytene stage, γH2AX disappears from synapsed autosomes and is restricted to the unsynapsed sex chromosomes in the sex body16. Herein we performed the immunohistochemistry (IHC) assay and our results showed that more than 60.0% tubules containing the germ cells with the entire nuclei stained by γH2AX in the Ndrg3+/− group, whereas this staining pattern was detected in 43.7% tubules in the wild type group (Fig. 4c and d). However, about 80% tubules contained the spermatocytes with the punctate positive staining indicating the γH2AX was restricted to the sex body region in the wild type group, whereas the number of these tubules was ~56% in the Ndrg3+/− group (Fig. 4c and e). These results suggested that the deficiency of Ndrg3 impairs DSB repairing in spermatocytes. We further studied the effect of NDRG3 on γH2AX distribution in meiotic male germ cells via spreading assay. We did not detect any significant different staining in the leptotene or early zygotene between the Ndrg3+/− and wild type group, suggesting the successful generation of DSB in Ndrg3+/− germ cells. At pachytene and diplotene stages, only the sex body (white dashed regions) was stained with γH2AX antibody, as expected, in the wild type spermatocytes, indicating that DSBs disappeared from the autosomes. However, the γH2AX foci remained on the autosomes at pachytene and diplotene stages in the Ndrg3+/− spermatocytes, indicating the presence of abnormal DSBs in the pachytene and diplotene in the Ndrg3 deficient mice. Additionally, some autosomes were also observed in the γH2AX staining sex body region in some pachytene and diplotene spermatocytes in the Ndrg3+/− group (Fig. 4f). The number of the spermatocytes at pachytene and diplotene stage with abnormal staining of γH2AX were significantly higher in the Ndrg3+/− than in wild type group, respectively (Fig. 4g and h). These results suggested that the deficiency of Ndrg3 impairs DSB repair in spermatocytes. In zygotene, repair of meiotic DSBs occurs, concomitant with the pairing of homologous chromosomes. Thus an examination of RAD51, a DNA repair marker, was performed between the Ndrg3+/− and wild type spermatocytes. A decreased number of the RAD51 foci was observed in Ndrg3+/− spermatocytes compared to the wild type group (Fig. 4i and j), strongly suggesting that the haplo-insufficiency of Ndrg3 led to the impaired DSB repair. The quantification of the indicated protein levels by western blot assay further confirmed the down-regulated DSB repair ability and abnormal DSB retention in the Ndrg3+/− testes (Fig. 4k). We also analyzed the homologous chromosomes synapsis (SYCP1) and crossover (MLH1) markers, but no significant difference was detected between the Ndrg3+/− and wild type groups (Supplemental Figure 3). Collectively, our results demonstrated that the deficiency of Ndrg3 gene resulted in the impaired DSB repair ability in zygotene, subsequently resulting in an abnormal presence of DSBs at the stages of pachytene and diplotene in meiosis I which was followed by a disturbed meiosis progression in male mice.
DSB repair required the lactate induced ERK1/2 signaling
Lactate, binding with NDRG3, a common product of anaerobic metabolism, not only protects NDRG3 from proteasomal degradation, but also activates the ERK1/2 pathway in the hypoxia responses21. Here, we confirmed that the lactate activated the ERK1/2 signaling in male germ cells in vitro. As was shown, after added to the cultured primary germ cells, lactate raised the level of pERK1/2 in the wild type male germ cells (Fig. 5a and b). Additionally, Fig. 5b showed that the lactate enhanced the NDRG3 protein level in a dose-depending way, which strongly suggested the inhibitory role of lactate to the NDRG3 proteasomal degradation.
As the MAPK cascade plays complicated roles in meiosis in the male germ cells36,37,38. In order to explore whether the lactate-NDRG3-ERK1/2 axis is required in DSB repair, we measured the expression of some associated genes during meiosis in vitro. Our real-time PCR assay showed the mRNA levels of Rad50, Mre11, Rad51 and Dmc1 were increased significantly after the treatment with lactate (Fig. 5c), suggesting that lactate participated in the DSB repair via up-regulating the associated genes.
To test whether the DSB repair requires the ERK signal in male germ cells, we isolated the male mouse germ cells and cultured with (15 μM and 30 μM) or without (0 μM) the ERK signal inhibitor U0126. Then real-time PCR assay detected the decreasing of Rad50, Mre11, Rad51, Dmc1, Brca1 and Brca2 (Fig. 5d). The down regulation of the above genes suggested the ERK signal was required for DSB repair. The ERK inhibition effect of U0126 was shown by western blot assay (Supplemental Figure 4). The co-effect of U0126 and lactate on DSB repair was analyzed by the real-time PCR assay, a majority of DSB repair associated genes was not induced by lactate in the U0126 treated male germ cells in vitro (Fig. 5e), indicating that the lactate induced DSB repair required the activation of ERK1/2 signaling. The protein level of RAD51 was measured in the Ndrg3+/− and wild type spermatocytes in vitro. The down-regulation of the meiosis associated proteins (Fig. 5f and Supplemental Figure 5) and other DSB repair related genes (Fig. 4a) in Ndrg3 deficient testes implied that NDRG3 influences the ERK1/2 signaling. We then compared the levels of pERK1/2 between the Ndrg3+/− and wild type testes. As was expected, the level of pERK1/2 was lower in the Ndrg3+/− than in the wild type groups (Fig. 5g), suggesting an attenuated ERK activation resulted from Ndrg3 deficiency in mouse testis.
Ndrg3 gene modulated the ERK1/2 signaling in the DSB repair
We hypothesized that NDRG3 played its meiosis-regulating role in a lactate-dependent way. In the cultured primary testicular cells from 6–8 week-age mice, we found that the pERK1/2 pathway (ERK1/2-pCREB) was enhanced apparently in the wild type germ cells, whereas the pERK1/2 in Ndrg3+/− germ cells was up regulated slightly after the treatment of lactate (30 mM) (Fig. 6a), suggesting NDRG3 is required for the lactate-induced activation of ERK1/2.
The mRNA levels of meiosis-associated genes were then examined by the real-time PCR assay. With the treatment of lactate, the DSB repair related genes such as Rad50, Mre11, Rad51, Dmc1, Brca1 and Brca2 were increased significantly in the wild type group. But the expressions of these genes were improved in various degrees in Ndrg3+/− germ cells (Fig. 6b). Then a longer time treatment of lactate with the spermatocytes were performed between the Ndrg3+/− and wild type groups in vitro (>36 hours). Some of the DSB repair genes were improved largely both in the wild type and Ndrg3+/− spermatocytes (for example, Rad51). Figure 6c showed the mRNA level of Rad51 were increased dramatically both in the Ndrg3+/− and wild type spermatocytes significantly. Note 4 fold increase of Rad51 mRNA detected in the Ndrg3+/− spermatocytes with the lactate treatment. Additionally, immunofluorescence assay showed the number of RAD51 foci increased obviously both in wild type and Ndrg3+/− spermatocytes, but the number of the foci was still less in the Ndrg3+/− group than that in wild type group under the treatment of lactate (Fig. 6d and e). These results gained in vitro suggested that insufficiency of NDRG3 impaired the lactate-responsive DSB repair.
To investigate how lactate-ERK-pCREB pathway influences the DSB repair, some DSB repair genes’ promoter regions were analyzed in silico. Three putative CRE (pCREB binding site) sequences (TGACGTCA) were found in the promoter region of Rad51 (−51/−56, −109/−114, −228/−233). One of the three putative CREs (−51/−56) located in a high conserved region (Fig. 6f). Thus we hypothesized that the pCREB binds to the CREs (−51/−233) in the Rad51 promoter. CHIP-qPCR assay showed U0126 significantly repressed the binding of pCREB to this promoter region approximately by 30% (Fig. 6g). These results demonstrated that the ERK-CREB signaling mediated the DSB repair by regulating the transcript level of Rad51.
Taken together, our present data demonstrated that the Ndrg3 gene regulated the expression of Rad51and the DSB repair via modulating the lactate-induced pERK1/2 signal pathway in the mouse male germ cells (Fig. 6h).
Although NDRG3 expresses highest in testis both in human and mouse, its physiological function has not been reported. In this present study, we demonstrated that NDRG3 plays an important role in DSB repair during the meiotic prophase I in testis.
Testis is a naturally oxygen-deprived organ in which lactate is the central energy metabolite for male germ-cell39. In testis, lactate also plays other key roles more than just serves as a substrate in metabolism. Previous reports showed that the lactate, which exerted an anti-apoptotic effect on germ cells40, was responsible for RNA and protein synthesis and improved spermatogenesis41. However, the elucidation of how lactate exerts its role in spermatocytes exactly is still very limited. NDRG3 has been reported to be bound to lactate, and then activate the Raf-ERK pathway in hypoxia21. Here, we established the Lactate-NDRG3-ERK1/2-CREB-RAD51 regulatory pathway in male germ cells, in which lactate not only stabilized NDRG3 protein, but also activated ERK signaling in an NDRG3-dependent way. Activation of ERK signaling transcriptionally raised the expression of RAD51 via phosphorylating CREB. Therefore, this pathway represented a new mechanism in DSB repair. Interestingly, our study also revealed a functional link between metabolism and the high expression of NDRG3 in testis. We observed that lactate improved the stability of NDRG3, which provided a piece of evidence for why NDRG3 expression is high in testis.
DSBs are formed by the induction of type II-like topoisomerase SPO1142 during the meiotic prophase I. Non-homologous end joining (NHEJ) and homologous recombination (HR) are two major mechanisms applied in DSB repair. MRN complex (consisting of MRE11, RAD50 and NBS1) and a number of kinases (such as ATM, ATR and DNA PKcs) are involved in DNA replication, DNA repair, and signaling to the cell cycle checkpoints43. In the in vitro assay, we revealed that NDRG3 mediated the DSB related genes via modulating lactate-ERK signaling. However, it should be mentioned that the mRNA levels of the DSB repair related genes (Rad50, Mre11, Dmc1 and Rad51) were partially rescued after the treatment of lactate in the Ndrg3+/− group compared with the wild type germ cells indicating that NDRG3 participated more than one signal pathway. The lactate-ERK independent transcription of Sycp1 and Sycp3 showed in the in vitro assay, together with the down-regulation of the transcript levels of meiosis associated genes (Sycp1, Sycp3, Fzr1 and Rec8) detected in vivo further supported this above speculation.
Interestingly, the fertility of male Ndrg3+/− mouse was recovered after 10–12 weeks age (Supplemental Figure 6). The phylogenetic analysis of the NDRG gene family demonstrated that the NDRG1 and NDRG3 belonged to one subfamily44,45. Along with the published data that NDRG1 was up-regulated under hypoxia46, therefore, we think NDRG1 might compensate the effect resulted from the deficiency of NDRG3. As a piece of supporting evidence for the hypothesis, we detected that expression of Ndrg1 was up-regulated after 36 and 48 dpp (Supplemental Figure 7), while the up-regulation of NDRG1 did not exist when NDRG3 mediating the spermatogenesis progression during the first wave.
Numerous studies showed that the activation of ERK signaling either inhibited or promoted the DNA repair according to different cells38,47,48,49. An aberrant up-regulation of EGFR signaling in the male germ cells was shown recently to impair the DSB repair with the down regulation of DNA-dependent kinase activation and over-staining of the γH2AX signals, indicating that the hyper-activation of MAPK cascade inhibited the DSB repair in meiosis38. In the present study, we showed the requirement of ERK signal pathway during the DSB repair. Inactivation of ERK1/2 cascade impaired the DSB repair with an abnormal retention of the γH2AX signal in male germ cells in vivo and decreased a series of DSB repair associated genes. Therefore, we provided a new mouse model showing that hypo-activation of MAPK cascade also affected the DSB repair during meiosis. In a rational manner, it may be speculated that the MAPK cascade is regulated precisely in germ cells, while those factors/chemicals which caused hyper- or hypo-activation of MAPK cascade will eventually result in the failure of DSB repair.
In summary, we have established the Lactate-NDRG3-ERK1/2-CREB-Rad51 regulatory pathway, which plays an important role in the first wave spermatogenesis. However, its significance in male infertility remains unknown and is worth a next approach. As the clinical data have showed a high prevalence of the subfertility was with metabolite disorders50, thus a further identification of the NDRG3 interacted proteins and the regulating mechanisms will make a significant contribution to a deeper understanding of male sub-infertility.
Materials and Methods
For fertility testing, 5 to 8 weeks old Ndrg3+/− or the wild type males were housed with 6 weeks old wild type C57BL/6 females primed with PMSG (5U) and hCG (5U). The number of the offspring from each pregnant female was counted after birth. All mice were kept under the controlled photoperiod conditions (lights on 07:00–19:00) and supplied with food and sterilized H2O ad libitum. All experiments were conformed to the regulations drafted by Association for Assessment and Accreditation of Laboratory Animal Care in Shanghai and were approved by the Shanghai Institute of Planned Parenthood Research Center for Animal Research.
Epididymides were removed from the wild type and Ndrg3+/− mice, incised and incubated in 1 ml buffer containing 75 mM NaCl, 24 mM EDTA, and 0.4% bovine serum albumin (Sigma, A2058) at 34 °C with 5% CO2 for 5 minutes to allow sperm to release. The suspension containing sperms was collected and counted with a CASA system (IVOS II Sperm Analyser, Hamilton).
Hematoxylin and eosin (H&E) staining, immunohistochemistry (IHC)
Testes were collected and immediately fixed in Bouin’s solution for H&E staining and fixed in 4% paraformaldehyde (PFA) for immunohistochemistry. For IHC assay, sections (4–5 μm) were deparaffinized in xylene and rehydrated in gradient alcohols. After antigen retrieval, the blocked sections were incubated with primary antibodies overnight at 4 °C. The sections were incubated with secondary antibodies for 20 minutes the next day and then developed with DAB and counterstained with hematoxylin. Antibodies were diluted as follows: NDRG3, at 1:100 (Santa Cruz Biotechnology), γH2AX (Abcam) at 1:1000. To ensure reproducibility of the results, samples from ≥3 animals were used.
Meiotic prophase cell spreading and immunofluorescence staining
Spreads of spermatocytes and immunofluorescence staining were prepared according to the previous references51,52. Briefly, seminiferous tubules were incubated in hypotonic extraction buffer (50 mM Sucrose, 17 mM Sodium citrate, 30 mM Tris (pH 8.2), 2.5 mM DTT, 1 mM PMSF (pH 8.3) and 5 mM EDTA on ice for 20 minutes, minced in 100 mM sucrose, spread on slides and fixed in 1% PFA with 0.1% Triton X-100. Slides were incubated in a humid chamber overnight, dried, and washed in PBS and water containing Photoflo (Kodak, NY, USA). Following blocking in 10% donkey serum and 3% BSA, immunofluorescence staining was performed by incubating with primary antibodies: γH2AX (1:500; abcam) and SYCP3 (1:100; Abcam) overnight at room temperature. Alexa 488 donkey anti-rabbit (1:500, Molecular Probes), Alexa 594 goat anti-mouse (1:200, Molecular Probes) were used as secondary antibodies. Slides were incubated with secondary antibodies at 37 °C for 1 hour in the dark, washed and mounted with Vecta shield cover slips. (Vector Laboratories).
Primary germ cell preparation
Testicular cells were obtained as previously described53. Briefly, the capsules of the testis were removed and the testicular tubules were minced and transferred to a 50 mL Falcon tube. Tissue was suspended in F12/DMEM (Gibco), centrifuged, collected, and then subjected to digestion. Use trypsin/EDTA (0.1 mg/mL; Sigma), DNase (0.02 mg/mL; Sigma), glycine (1 M; Sigma), EDTA (2 mM; Sigma) and STI (0.1 mg/mL; Sigma) to eliminate Leydig cells. Use Collagenase 1 A (0.1 mg/mL; Sigma) and DNase (5 μg/mL; Sigma) to reduce peritubular cells. Then testicular cells were washed and plated in medium with gentamicin (0.02 g/L; Sigma), maintained in a humidified atmosphere at 34 °C with 5% CO2 for 6–8 hrs. Germ cells were harvested by gentle shaking and suction gently54. The residual aggregate was consisted of sertoli cells (SC). To collect the spermatogonia (SPG), 7–8 dpp male mice were employed. For the sub-group meiosis prophase I spermatocytes, the method of STA-PUT was used and cells were isolated according to the diameters. leptotene (LS): 8–10 μm, zygotene (ZS): 10–12 μm, and pachytene & diplotene (PDS): 14–18 μm. Spermatids (SPD) were isolated by the method of flow cytometry with the Hoechst 33342 staining. According to a published report55, the identification of the testicular cells were showed in Supplemental Figure 8.
RNA isolation and real-time PCR
Total RNA was extracted from the wild type and Ndrg3+/− mouse indicated, tissues or isolated primary cells homogenized in TRIzol reagent (Invitrogen), followed by RNA precipitation. cDNA was synthesized with a reverse transcription kit (TaKaRa). Real-time PCR was performed using SYBR Premier EX Taq (TaKaRa). Genes were amplified with the indicated primers (Supplemental Table). Relative levels of mRNAs were calculated using MX3500pro software and normalized to the levels of endogenous β-Actin in the same samples.
Tissue or cell extracts containing 30 μg proteins were resolved by SDS-PAGE and transferred to nitrocellulose (NC) membrane (Millipore Corp). After probing with primary antibodies, the membranes were incubated with Odyssey fluro-800–conjugated anti-rabbit/mouse IgG antibodies (Li-Cor). The primary antibodies used were NDRG3 (Santa Cruz Biotechnology, 1:1000), pERK1/2 (CST, 1:1000), ERK1/2 (CST, 1:1000) and β-Actin (Sigma, 1:10000).
Germ cells cultured were treated with or without U0126 (15 μM) overnight. Cells were harvested and DNA was precipitated with a polyclonal anti-pCREB antibody, or mouse IgG as a negative control. Precipitated DNA was amplified with the following primer sets for the Rad51 promoter region: P1 5′-ATTCTGGGTTATGTAGTCCT-3′ (upper) and P2 5′-TCCCGCCAAATCCTCACGCT-3′ (lower). The PCR products were confirmed by sequencing.
All statistical data were analyzed with GraphPad Prism version 5. The statistical data of litter sizes, sperm number, testis weight, testosterone levels, number of spermatocytes cells and relative mRNA expression were presented as means ± SEM. ANOVA or Student’s t test were used for statistical comparison to determine significance. The difference of the number of spermatogonium, MMI and MMII cells as well as the ratios of MMII to MMI were tested for significance using the Mann-Whitney U-test as described previously32. Statistical significance set: NS, P > 0.05; *P ≤ 0.05; **P ≤ 0.01. All presented results were from at least 3 independent experiments.
How to cite this article: Pan, H. et al. Ndrg3 gene regulates DSB repair during meiosis through modulation the ERK signal pathway in the male germ cells. Sci. Rep. 7, 44440; doi: 10.1038/srep44440 (2017).
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We thank Prof. Minghan Tong, who is a PI in Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, for his helpful discussions. This work was supported by grants from the National Natural Science Foundation of China (grant no. 81270760 (RL), 81571495 (RL), 31630050 (QS), 31371519 (QS), 31501199 (XJ)), the National Basic Research Program of China (grant 2014CB943104 (RL)), Shanghai Municipal Committee of Science and Technology (grant nos 14ZR1435400 (HP), 15431902800 (RL) and 15140903100 (RL)), Shanghai Municipal Commission of Health and Family Planning (20144Y0211 (HP)).
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