To explore the function of Srsf10 in male fertility and spermatogenesis, we mated Srsf10^{Floxed/Floxed} (Srsf10^F/F) mice, in which the exon 3 (104 bps) was flanked by two loxP sites, with Vasa-Cre transgenic mice in which the Cre recombinase driven by a Vasa promoter is specifically expressed in germ cells as early as E15 (Gallardo et al., 2007; Figure 1A, Figure 1—figure supplement 1A and B). Srsf10^F/+;Vasa-Cre males and Srsf10^F/F females were used for breeding, and the progeny was used for further experimental analysis (Figure 1—figure supplement 1A and B). Four genotypes of mice, including Srsf10^F/+, Srsf10^F/−, Srsf10^F/+;Vasa-Cre, and Srsf10^F/−;Vasa-Cre, were obtained and verified by PCR (Figure 1—figure supplement 1B and C). SRSF10 expression was barely detected in Mouse Vasa Homologue (MVH)-positive germ cells of Srsf10^F/−;Vasa-Cre (hereafter referred to as Srsf10-cKO) mice at postnatal day 8 (P8) (Figure 1B), confirming Srsf10 was specifically depleted in germ cells at P8.

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The testis weight and the number of PLZF+ cells of adult male mice.

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The 2-month-old Srsf10-cKO males looked grossly normal. Normal copulatory plugs could be observed when adult Srsf10-cKO males were mated with ICR wild-type females, but no pups were obtained (Table 1), indicating that Srsf10-cKO males were infertile. Compared to that of 2-month-old Srsf10^F/+ or Srsf10^F/+;Vasa-Cre mice, the testes of Srsf10-cKO males were much smaller (Figure 1C). The weight of testes and ratio of testes to body weight in Srsf10-cKO males were significantly reduced (Figure 1D and E). We then analyzed the histology of 2-month-old Srsf10^F/+, Srsf10^F/+;Vasa-Cre mice, and Srsf10-cKO testes using hematoxylin and eosin (H&E) staining. While all populations of spermatogonia, spermatocytes, and spermatids were observed in Srsf10^F/+ or Srsf10^F/+;Vasa-Cre mice seminiferous tubules, no spermatocytes and spermatids could be observed in the center of seminiferous tubules from Srsf10-cKO testes (Figure 1F). Moreover, no mature spermatozoa could be found in the cauda epididymis of Srsf10-cKO mice (Figure 1F). To further identify the remaining germ cells in Srsf10-cKO testes, we co-stained these germ cells with MVH and PLZF (the marker of all undifferentiated spermatogonia; Buaas et al., 2004). Immunofluorescence results showed that the MVH⁺ and PLZF⁺ cells were comparable in 2-month-old Srsf10^F/+ and Srsf10^F/+;Vasa-Cre mice (Figure 1G). As Srsf10^F/+ and Srsf10^F/+;Vasa-Cre mice were healthy and phenotypically normal, Srsf10^F/+;Vasa-Cre mice (hereafter, ‘control’) were used as control in the following experiments unless otherwise noted. Only sporadic MVH⁺PLZF⁺ cells can be detected around the basement of seminiferous tubules from 2-month-old Srsf10-cKO testes (Figure 1G). Statistical analysis showed that the number of PLZF⁺ cells was significantly reduced in 2-month-old Srsf10-cKO testes compared to the control (Figure 1H), suggesting that only a few PLZF⁺ undifferentiated spermatogonia were left in the adult Srsf10-cKO testes. Similarly, testes from 1-month-old Srsf10-cKO were also much smaller, and spermatocytes were absent (Figure 1—figure supplement 2). Taken together, these data demonstrate that Srsf10 is essential for male fertility and spermatogenesis.

As no spermatocytes were observed in the seminiferous tubules of 2-month-old and 1-month-old Srsf10-cKO testes, we speculated that the meiosis process may be failed in Srsf10-cKO mice. To figure out which stage in spermatogenesis was affected after Srsf10 deletion, we carefully analyzed the sections from P8, P10, P12, and P15 testes using H&E staining (Ahmed and de Rooij, 2009). At P8, type A spermatogonia (A), intermediate spermatogonia (In), and type B spermatogonia (B) could be observed in both control and Srsf10-cKO testes. Afterward, some germ cells entered into meiosis and developed into leptotene spermatocytes in P10 control testes, and abundant zygotene and pachytene spermatocytes could be observed in P12 and P15 control testes (Figure 2A). However, rare meiotic spermatocytes were detected in the seminiferous tubules of P10, P12, and P15 Srsf10-cKO testes (Figure 2A), suggesting that meiosis initiation might be impaired in Srsf10-deleted mice.

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The ratio of SYCP3⁺ tubule cross-sections in P12 testes.

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RAW western blot for γH2AX, SRSF10, and β-actin.

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To further confirm the above results, we co-stained MVH and SYCP3, which was a component of the synaptonemal complex and the marker of meiosis prophase I at P12. Spermatocytes in the vast majority of control seminiferous tubules had entered into meiotic prophase I as expected, and abundant MVH⁺SYCP3⁺ germ cells could be detected in the center. However, only very few seminiferous tubules contained a tiny minority (about 3–5) of MVH⁺SYCP3⁺ germ cells could be observed in Srsf10-cKO testes (Figure 2B). Statistically, the ratio of SYCP3⁺ seminiferous tubule cross-sections in Srsf10-cKO testes was significantly lower than the control at P12 (16.41%±4.79 vs 81.45%±4.33, mean ± SEM) (Figure 2C). Next, we detected the expression of the marker of homologous recombination γH2AX, which can be another indicator of meiosis, in P12 testes. Immunofluorescence results showed that γH2AX⁺ cells were nearly undetectable in the seminiferous tubules of Srsf10-cKO testes (Figure 2D). Western blot showed that γH2AX was markedly elevated in control testes from P10 to P12, consistent with the entering into meiotic prophase I of many spermatocytes around this time. However, the expression of γH2AX changed little in Srsf10-cKO testes from P8 to P12 (Figure 2E), indicating failure of meiosis entrance. These results indicate that Srsf10 deletion causes a severe defect in meiosis initiation during spermatogenesis.

Before meiosis, SSCs proliferate to self-renew or generate differentiation-committed progenitors. The progenitor spermatogonia respond to the RA signal and divide into KIT⁺ differentiating spermatogonia (Figure 3A). Then type B differentiating spermatogonia further proliferate and differentiate into meiotic spermatocytes. Therefore, the initiation of meiosis requires several rounds of mitotic divisions of progenitors for full expansion and efficient differentiation (Song and Wilkinson, 2014; Niedenberger et al., 2015; Busada et al., 2015). Interestingly, we found that the expression of MVH and PLZF was significantly reduced in Srsf10-cKO testes from P8 to P12 (Figure 3B). Co-staining of MVH and PLZF showed that the number of PLZF⁺ undifferentiated spermatogonia was apparently reduced in Srsf10-cKO testes at P12 (Figure 3—figure supplement 1A and B). These results indicate that loss of Srsf10 affects the normal development of spermatogonia, which may further lead to the failure of meiosis initiation.

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RAW western blot for MVH, PLZF, and β-actin.

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Quantification of MVH⁺, MVH⁺PLZF⁺, or MVH⁺PZF⁻ cells per tubule cross-section and KIT⁺ or GFRα1⁺ cells per 100 μm seminiferous tubule.

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Considering the loss of PLZF⁺ cells in P12 Srsf10-cKO testes, we speculated that the proliferation and thus the differentiation of progenitors may be affected when Srsf10 is depleted. Therefore, we analyzed the distribution and the number of both undifferentiated and differentiating spermatogonia in control and Srsf10-cKO testes at P8 and P6, when only spermatogonia and Sertoli cells can be observed in the seminiferous tubules. At P8, co-staining for MVH and PLZF showed that numerous differentiating spermatogonia (MVH⁺PLZF⁻) could be detected at the basement of seminiferous tubules in control. However, MVH and PLZF were largely co-localized in Srsf10-cKO testes, indicative of few differentiating spermatogonia (MVH⁺PLZF⁻; Figure 3C). Statistical analysis showed that differentiating spermatogonia (MVH⁺PLZF⁻) were nearly absent, and the number of undifferentiated spermatogonia (MVH⁺PLZF⁺) was significantly reduced in Srsf10-cKO testes compared to the control (Figure 3C). We further performed whole-mount staining of the testes for the differentiating spermatogonia expressing KIT. The number of KIT⁺ cells was obviously reduced in Srsf10-cKO testes compared to the control at P8 (Figure 3D), further confirming the lack of differentiating spermatogonia. At P6, co-staining for MVH and PLZF showed that most of the germ cells were undifferentiated spermatogonia (MVH⁺PLZF⁺) in both control and Srsf10-cKO testes (Figure 3E). However, the number of the undifferentiated spermatogonia (MVH⁺PLZF⁺) was also significantly reduced in Srsf10-cKO testes compared to the control (Figure 3E). PLZF is a broader marker of all undifferentiated spermatogonia including As, Apr, and Aal spermatogonia (Figure 3A). Thus, we performed whole-mount staining for GFRα1, which is specifically expressed in As and Apr spermatogonia (Sada et al., 2009; Grasso et al., 2012). The GFRα1⁺ cells were also reduced in Srsf10-cKO testes compared to the control at P6 (Figure 3F). Altogether, these results suggest that fewer PLZF⁺ undifferentiated progenitors (maybe also including GFRα1⁺ SSCs) are produced in the absence of Srsf10 as early as P6.

Because Vasa-Cre recombinase is expressed as early as E15.5, we examined the number of germ cells in both control and Srsf10-cKO testes at P3. There was no difference in germ cell numbers between control and Srsf10-cKO testes (Figure 3G). Interestingly, from P3 to P12, the number of PLZF⁺ undifferentiated spermatogonia was gradually increased in both control and Srsf10-cKO testes. However, the kinetics in Srsf10-cKO testes was much slower, leading to a comparable number of PLZF⁺ cells per tubule cross-section in P12 Srsf10-cKO to that in P6 control testes (Figure 3H). Western blot confirmed that the expression of PLZF in P3 testes was lower, and no significant difference was observed between control and Srsf10-cKO testes. With the resumption of mitosis, the expression of PLZF was apparently increased from P3 to P8 in control testes but was only slightly increased in Srsf10-cKO testes (Figure 3—figure supplement 1C). All these data suggest that Srsf10 may be essential for the expansion of the progenitor spermatogonia population, disturbance of which may further lead to differentiation defect.

To systematically investigate the molecular effects of Srsf10 loss in germ cells, we compared the transcriptomes of control and Srsf10-cKO testes at P3, P6, and P8. RNA-seq analyses identified only 10 upregulated and 9 downregulated genes in Srsf10-cKO testes compared with the control at P3 ( fragments per kilobase of exon per million reads mapped [FPKM] ≥5, fold change ≥2, and p<0.01; Figure 4A), suggesting that the transcriptome is largely normal at P3 in Srsf10-depleted testes. This is consistent with the immunostaining result showing that the number of germ cells is comparable between control and Srsf10-cKO testes at P3. However, 138 genes were differentially expressed between the control and Srsf10-cKO testes at P6, and nearly all genes (135/138) were downregulated in Srsf10-cKO testes (Figure 4A). 396 genes were differentially expressed in Srsf10-cKO testes at P8, including 243 upregulated and 153 downregulated genes (Figure 4A). Surprisingly, only 57 genes were commonly downregulated in the Srsf10-cKO testes at both P6 and P8 (Figure 4B). GO analysis of the 57 genes showed that these genes are involved in the meiotic cell cycle, spermatogenesis, cell differentiation, and germ cell development (Figure 4B). We then systematically analyzed the expression pattern of all downregulated genes in control and Srsf10-cKO testes from P3 to P8. The vast majority of downregulated genes were gradually increased from P3 to P8 (Figure 4—figure supplement 1A). Interestingly, many genes that were only significantly downregulated at P6 (e.g. Pou5f1, Sohlh1, Egr4, Nanos3, Foxc2, and Sox3) were mainly involved in the expansion and early differentiation of progenitor spermatogonia (Figure 4B). The expression level of these genes was very low in P6 Srsf10-cKO testes and somewhat upregulated afterward in P8 Srsf10-cKO testes (Figure 4—figure supplement 1A). Many genes that were only significantly downregulated at P8 (e.g. Kit, Sycp3, Sycp2, Atm, and Rec8) were involved in spermatogonia differentiation and meiosis and were barely upregulated in Srsf10-cKO testes from P6 to P8 (Figure 4B and Figure 4—figure supplement 1A), echoing nearly no differentiating spermatogonia and meiotic spermatocytes in P8 Srsf10-cKO testes. Unsupervised cluster analysis of spermatogonia-specific genes (SPGs; Green et al., 2018) showed that the gene expression pattern of Srsf10-cKO testes at P8 was much more similar to that of control testes at P6 (Figure 4C), consistent with the compromised and slower expansion and differentiation of progenitor spermatogonia in the Srsf10-cKO testes than control.

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List of the differential expression genes in control and Srsf10-cKO testes at P3, P6, and P8, respectively.

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Validation of the expression of marker genes in control and Srsf10-cKO testes using qRT-PCR at P6.

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We then analyzed several marker genes for stem cell maintenance, expansion, and differentiation of the spermatogonia population. Most genes involved in SSCs maintenance (Etv5, Bmi1, Id4, Lhx1, Cd82, and T) were hardly affected in the Srsf10-cKO testes from P3 to P8. However, genes associated with progenitor spermatogonia (Lin28a, Nanos3, Sox3, Neurog3, Pou5f1, and Sohlh1), undifferentiated spermatogonia (Zbtb16 (Plzf) and Sall4), and differentiating spermatogonia (Dmrtb1, Dnmt3b, Stra8, Kit, and Prdm9) were downregulated in Srsf10-cKO testes at P6 and P8 compared to control (Figure 4D and Figure 4—figure supplement 1B). The qRT-PCR results also confirmed that the expression of genes involved in the expansion and differentiation of progenitor cells was globally reduced in P6 Srsf10-cKO testes (Figure 4E). Taken together, these data suggest that Srsf10 deficiency disturbs genes involved in progenitor spermatogonia and thus their expansion and differentiation.

To address the heterogeneity of spermatogonia after Srsf10 depletion, we sought to enrich the undifferentiated and differentiating spermatogonia using their cell surface markers, THY1 (undifferentiated spermatogonia) and KIT (differentiating spermatogonia). We enriched THY1⁺ KIT⁻, THY1⁻KIT⁺, and THY1⁺ KIT⁺ spermatogonia from control (one replicate isolated from three different mice) and Srsf10-cKO testes (two replicates isolated from six different mice) using magnetic-activated cell sorting (MACS) with anti-THY1 and anti-KIT antibodies at P8 (Oatley et al., 2006). The isolated single cells were subjected to single-cell RNA-seq analysis using the 10× Genomics platform (Figure 5A). After filtering out low-quality cells, 1157 control and 766 Srsf10-cKO spermatogonial cells were used for further analysis. Clustering analysis identified five distinct spermatogonial subtypes/states as visualized using uniform manifold approximation and projection (UMAP; Becht et al., 2018; Figure 5B). Based on known cell type markers, we named these cell clusters USPG1 (undifferentiated spermatogonia 1), USPG2, DSPG1 (differentiating spermatogonia 1), DSPG2, and DSPG3 (Figure 5B). USPG1 cells corresponded to SSCs, as they highly express SSC marker genes, including Eomes, Id4, Lhx1, Etv5, Gfra1, and Smoc2 (Figure 5C and Figure 5—figure supplement 1). USPG2 cells were highly enriched for Nanos3, Pou5f1, and Zbtb16 (Plzf), with increased levels of Sox3 and Sohlh1, but lower levels of SSC-associated markers and differentiation markers (Figure 5C and Figure 5—figure supplement 1), corresponding to early progenitor spermatogonia. By contrast, DSPG1 cells expressed high levels of early differentiation marker genes such as Stra8, Sox3, Sohlh1, Sohlh2, and Dmrt1 and low levels of Pou5f1, Nanos3, and Zbtb16 (Figure 5C and Figure 5—figure supplement 1), indicating that this cell population is likely late progenitor/early differentiating spermatogonia. DSPG2 cells displayed lower Stra8 expression but mainly expressed differentiation marker genes including Kit, Dmrtb1, Cited1, and Dmrt1 (Figure 5C and Figure 5—figure supplement 1), implicating them as differentiated spermatogonia. The DSPG3 cluster was only observed from the Srsf10-cKO group. These cells express some differentiating markers such as Stra8, Dmrt1, Sohlh2, and Kit, but the expression level of Stra8 and Kit was lower than DSPG1 and DSPG2, respectively (Figure 5C), suggesting that DSPG3 cells might have differentiated but with abnormal development. The pseudotime analysis provided a trajectory indicating the development of germline cells from USPG1 to DSPG2 (Figure 5D).

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We then asked whether and how the subtypes of spermatogonia changed after Srsf10 depletion. We found that USPG1 (17.5%, 203 cells), USPG2 (20.2%, 234 cells), DSPG1 (23.6%, 273 cells), and DSPG2 cells (38.6%, 447 cells) were largely evenly distributed in the control group (Figure 5E). By contrast, the proportion in the Srsf10-cKO group was severely slanted, which was manifested by the dramatic decrease of USPG2 (8.1%, 62 cells), DSPG1 (11.6%, 89 cells), and DSPG2 (20.3%, 156 cells) subtypes, and the dominance of the USPG1 subtype (35.6%, 273 cells). On the other hand, 24.3% (186 cells) of the cells were sorted into the DSPG3 subtype, which was scattered in the other 4 spermatogonial subtypes (Figure 5E). These data suggest that Srsf10 deficiency severely impairs the development of spermatogonia. Taken together, single-cell transcriptional analysis of spermatogonia shows that the progenitor and differentiating spermatogonia are largely lost in Srsf10-cKO testes at P8, further confirming the requirement of Srsf10 for the expansion of progenitor spermatogonia.

We then analyzed the differentially expressed genes in the aforementioned four subtypes of cells between the control and Srsf10-cKO samples. In USPG1, 184 and 175 genes were downregulated and upregulated, respectively (|log2FC|>0.25 and p<0.01; Figure 6A). The downregulated genes were mainly enriched for cell cycle, chromosome segregation, mitotic spindle organization, spermatogenesis, and cell proliferation. The upregulated genes were enriched for G1/S transition of mitotic cell cycle, regulation of apoptotic process, and negative regulation of cell proliferation (Figure 6B). Consistently, Top2a, Mki67, Cdc20, Ccnb1, Ccna2, Cenpe, Rad50, Kif11, Nusap1, and Prc1, which are important for cell cycle and cell division, were significantly reduced in the USPG1 cells in the Srsf10-cKO sample (Figure 6B and C and Figure 6—figure supplement 1). Dnaja1, Aspm, Ccnb1, Btg1, Racgap1, Sycp1, Sycp3, and Mns1, which are required in spermatogenesis, were also significantly reduced in the USPG1 cells in the absence of Srsf10 (Figure 6B and C and Figure 6—figure supplement 1). In the USPG2, DSPG1, and DSPG2, the downregulated genes were also enriched for cell cycle, cell division, and cell proliferation (Figure 6—figure supplement 2). These data indicate that depletion of Srsf10 in germ cells likely disrupts the normal cell cycle and proliferation of spermatogonia.

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List of the differential expression genes in USPG1 and GO analysis of these differential expression genes.

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Quantification of the ratio of KI67⁺PLZF⁺ cells, EdU⁺PLZF⁺ cells, and CAP3⁺PLZF⁺ cells in PLZF⁺ cells in control and Srsf10-cKO testes.

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To test this idea, we first investigated the proliferation of spermatogonia in Srsf10-cKO testes by co-staining for PLZF and Ki-67 (labeling mitotic cells that are not in the G0 phase) to analyze the mitotic status of spermatogonia at P6. The immunofluorescence result showed nearly all PLZF⁺ cells were positive for Ki-67 in both control and Srsf10-cKO testes (Figure 6D). The number of Ki-67⁺PLZF⁺ cells was not significantly different between control and Srsf10-cKO testes (Figure 6E), suggesting that all the PLZF⁺ cells were in the mitotic status. We further tested the EdU incorporation of PLZF⁺ spermatogonia in the control and Srsf10-cKO testes at P6. EdU is a thymidine analog and can incorporate into the DNA molecule during S-phase. Control and Srsf10-cKO mice were intraperitoneally injected with EdU (5 mg/kg), and testes were collected 4 hr later for fixation and paraffin section. Co-staining for EdU and PLZF showed that the EdU incorporation was significantly reduced in Srsf10-cKO PLZF⁺ spermatogonia at P6 (Figure 6F and G). These results suggest that the proliferation of PLZF⁺ spermatogonia in Srsf10-cKO mice was significantly impaired. We also detected the EdU incorporation in spermatogonia expressing GFRα1 in the control and Srsf10-cKO testes at P3. Co-staining for EdU and GFRα1 showed that EdU incorporation of GFRα1⁺ cells was comparable in control and Srsf10-cKO P3 testes (Figure 6—figure supplement 3), suggesting that the proliferation of GFRα1⁺ SSCs was probably not much affected at P3.

As upregulation of apoptosis-related genes in the USPG1 and USPG2 cells, we also analyzed the apoptosis of PLZF⁺ spermatogonia. Double staining for cleaved caspase 3 (CAP3) and PLZF showed that the number of CAP3⁺PLZF⁺ spermatogonia was significantly higher in Srsf10-cKO testes compared to the control (Figure 6H and I), implying that the survival of spermatogonia was also impaired when Srsf10 is depleted. In conclusion, Srsf10 depletion might lead to abnormal cell cycle and mitotic division, and further affect the proliferation and survival of spermatogonia.

We then sought to probe into how Srsf10 depletion affects spermatogenesis at the molecular level. To this end, we collected the THY1⁺ spermatogonia using MACS from control and Srsf10-cKO testes at P6 to minimize the potential side effects (Oatley et al., 2006; Figure 7A). Flow cytometry and immunostaining analyses showed that the proportion of undifferentiated spermatogonia (THY1⁺ or PLZF⁺ cells) was significantly increased in the sorted group than that in the unsorted group (Figure 7—figure supplement 1A and B). We confirmed the dramatic decrease of Srsf10 in the enriched spermatogonia of Srsf10-cKO testes at both RNA and protein levels (Figure 7—figure supplement 1C and D). Next, we performed the linear amplification of complementary DNA ends and sequencing (LACE-seq) (Figure 7A; Su et al., 2021), a low-input method for global profiling of RBP target sites, to profile the SRSF10 binding events in the enriched spermatogonia. The LACE-seq data were highly reproducible between the two replications for SRSF10 (Pearson = 0.73) (Figure 7B, Figure 7—figure supplement 2A), which were pooled together for the following analyses. Most of the SRSF10 binding sites were in gene body regions, with 60.49% mapped to the exonic sequences (Figure 7C). SRSF10-binding peaks in mouse spermatogonia were significantly enriched for GA-rich consensus motif (GAAGAG) (Figure 7D), which was consistent with the motif analysis of RNA-seq data in chicken DT40 cells Zhou et al., 2014b. Further analysis showed that SRSF10 tended to bind exons and was enriched between 0 and 100 nt of the 5’ and 3’ exonic sequences flanking the constitutive splice sites (Figure 7E), presumably reflecting its roles in splicing. With a cutoff of FPKM ≥10, fold change ≥2 in both replicates, 1207 SRSF1-binding genes in THY1⁺ spermatogonia were identified (Figure 7—figure supplement 2B). These genes were significantly involved in chromatin organization, cell cycle, cellular response to DNA damage stimulus , stem cell population maintenance, spermatogenesis, and male meiosis (Figure 7F). These data indicate that SRSF10 functions as a crucial regulator by directly binding its targets in the development of spermatogonia.

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List of SRSF10 binding targets of LACE-seq data and GO analysis of the SRSF10 binding targets of LACE-seq data.

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To explore how SRSF10 is involved in gene regulation in spermatogonia development, we performed next-generation sequencing of the enriched THY1⁺ spermatogonia of P6 control and Srsf10-cKO testes (Figure 8A) and compared the transcriptome between them. RNA-seq analyses identified only 11 downregulated genes and 60 upregulated genes in Srsf10-cKO spermatogonia compared with the control using a commonly used cutoff (FPKM ≥5, |log2FC|≥1, and p<0.05). But if a lower cutoff (FPKM ≥2, |log2FC|≥0.5, and p<0.05) was used, 206 downregulated genes can be identified that were significantly enriched for spermatogenesis, meiotic cell cycle, cell differentiation, and male germline stem cell asymmetric division (Figure 8—figure supplement 1A). Among the 206 down-regulated genes were the markers of progenitor spermatogonia, such as Nanos3, Sox3, Lin28a, and Neurog3 (Figure 8—figure supplement 1A), presumably due to the absence of the progenitor spermatogonia, as observed in the scRNA-seq data. We compared the differentially expressed genes with 1207 targets in LACE-seq data and found that only 24 genes were overlapped (Figure 8—figure supplement 1B), suggesting that changes in gene expression might be regulated indirectly by SRSF10.

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Differential alternative splicing events in the Iso-seq data using SUPPA2 analysis and RNA-seq data using comprehensive AS Hunting analysis and raw GO analysis data of all 675 differential alternative splicing genes.

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Raw GO terms for 113 genes directly bound by SRSF10 with significantly affected AS events.

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Raw RT-PCR gel for Bclaf1, Nasp, Sycp1, Cenph, Rif1, and Mcm10.

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Raw western blot for BCLAF1, NASP, DAZL, and KAT7.

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Srsf10 is an SR protein and is involved in AS. We asked whether depletion of Srsf10 would affect the splicing and AS in spermatogonia. THY1⁺ spermatogonia at P6 were collected and subjected to PacBio isoform sequencing (Iso-seq) (Figure 8A), which can generate and capture the full-length cDNAs and present more accurate information about isoforms, alternatively spliced exons, and fused transcripts. We then analyzed the Iso-seq data for identification of the differentially spliced events (DSEs) between control and Srsf10-cKO spermatogonia using SUPPA2 software (Trincado et al., 2018). 522 DSEs in 417 genes were identified (p<0.05 and |ΔPSI|>0.1), the majority of which were exon skipping (191) (Figure 8—figure supplement 2A). Among the 522 DSEs, 266 AS events had negative ΔPSI values, and 256 had positive ΔPSI values, indicating that Srsf10 has no bias in the regulation of exon inclusion or exclusion (Figure 8—figure supplement 2B). Additionally, the RNA-seq data were analyzed for AS using Comprehensive AS Hunting (CASH) software, which is an AS event detecting method with a high rate of validation (Wu et al., 2018). 332 DSEs involved in 317 genes were identified (p<0.05), the majority of which were exon skipping (229) (Figure 8—figure supplement 2C). Combining the Iso-seq and RNA-seq data, we identified 675 abnormally spliced genes in the Srsf10-cKO spermatogonia (Figure 8B). GO analysis of the 675 genes showed that these genes were involved in cellular response to DNA damage stimulus, cell cycle, translation, mitotic G2/M transition checkpoint, DNA replication, and spermatogenesis (Figure 8—figure supplement 2D). These data indicate that SRSF10 functions as an important splicing regulator in mouse spermatogenesis. However, the functional consequences of these DSEs for genes themselves and specific cellular or developmental events warrant further investigation experimentally.

We then asked how these differentially spliced genes were regulated by SRSF10. Among the 675 differentially spliced genes, 113 genes were bound by SRSF10 as identified in LACE-seq (Figure 8B), indicating that these genes are probably the direct targets of SRSF10. The 113 genes were involved in RNA splicing, regulation of translation, chromosome segregation, synaptonemal complex assembly, mitotic spindle organization, and regulation of double-strand break repair (Figure 8C). Importantly, we successfully verified that loss of SRSF10 in spermatogonia resulted in differential splicing of exon 7 in Nasp (increased exon skipping), exon 6 in Sycp1 (increased exon skipping), alternative 3’ splice sites of exon 5 in Bclaf1, exon 32 in Rif1 (increased exon skipping), exon 8 in Cenph (increased exon skipping), and exon 5 in Mcm10 (increased exon skipping) (Figure 8D). The remaining 562 differentially spliced genes were not detectably bound by SRSF10 (Figure 8B), suggesting their altered splicing might be an indirect effect of SRSF10 depletion, for example, a secondary result of altered splicing of other splicing factors (e.g. RBM5, RBM19, and HNRNPC) in the absence of SRSF10 (Figure 8C). Some genes involved in important spermatogonia-related processes, including cell cycle and germ cell development were also successfully verified. For example, loss of Srsf10 resulted in differential splicing of exon 8 in Dazl (increased exon inclusion), alternative last exon in Ret, alternative 5’ splice sites of exon 9 in Kit (absence of four amino acids), exon 8 in Cdc7 (increased exon inclusion), exon 9 in Zfp207 (increased exon skipping), exon 14 in Kat7 (increased exon skipping), exon 7 in Ccna (increased exon skipping), alternative first exon in Ccne2, and alternative 5’ splice sites of exon 10 in Exo1 (Figure 8—figure supplement 3). Furthermore, we confirmed the corresponding changes at the protein level of the direct targets (Nasp and Bclaf1) and indirect targets (Dazl and Kat7) (Figure 8E). These data suggest that SRSF10 is required for the correct splicing of functional genes, thus maintaining the homeostasis of AS during spermatogenesis.

In adult testes, Srsf10 depletion mediated by Vasa-Cre leads to the absence of differentiating spermatogonia, with the existence of only fewer PLZF⁺ undifferentiated spermatogonia in adult testes, suggesting that the undifferentiated spermatogonia cannot undergo efficient expansion during SSC-dependent spermatogenesis. In the neonatal mice testes, the number of PLZF⁺ undifferentiated spermatogonia increases but at a much slower pace from P6 to P12, and differentiating spermatogonia and spermatocytes can barely be observed. This phenotype is much earlier and more severe than that of the depletion of genes that are important for the maintenance of SSCs (Etv5, Bcl6b, Id4, and Taf4b; Oatley et al., 2006; Oatley et al., 2011; Chen et al., 2005; Falender et al., 2005) or differentiation of spermatogonia (Sohlh1 and Sohlh2; Hao et al., 2008; Ballow et al., 2006). The former does not lead to infertility until adulthood and exhibits an age-dependent progressive loss of germ cells, while the latter leads to loss of differentiating spermatogonia but with limited effect on undifferentiated spermatogonia. So, the defects of Srsf10-cKO testes might mainly be due to failed self-renewal of SSCs and expansion of the progenitor spermatogonia population.

The number of GFRα1⁺ cells was decreased in P6 Srsf10-cKO testes, and SSC markers expression was not upregulated from P3 to P8, suggesting that loss of SRSF10 in spermatogonia might not cause the accumulation of SSCs. Although the ratio of USPG1 (SSCs) was increased in Srsf10-cKO samples as detected in the scRNA-seq data, it is more likely a result of the loss of progenitors (USPG2) and differentiating cells (DSPG1 and DSPG2).

scRNA-seq data showed that the expression of genes associated with the cell cycle in USPG1 (corresponding to SSCs) and USPG2 (corresponding to progenitor cells) was abnormal in Srsf10-cKO testes. However, EdU incorporation was reduced in PLZF⁺ spermatogonia in P6 Srsf10-cKO testes but was comparable between control and Srsf10-cKO GFRα1⁺ cells in P3 testes, suggesting that the cell cycle defect was more severe in the progenitor cells than in SSCs. This might be due to the faster proliferation rate of progenitor spermatogonia than SSCs which are normally quiescent and exhibit a very slow cell cycle rate (de Rooij and Russell, 2000). Additionally, the PLZF⁺ spermatogonia gradually increased, but at a slower pace, in Srsf10-cKO testes from P3 to P12, and the expression of genes involved in the expansion and early differentiation of progenitor spermatogonia was also somewhat upregulated from P6 to P8 Srsf10-cKO testes. Although we cannot fully exclude the possibility that the cell cycle defect in SSCs impedes the transition to progenitors, the significantly decreased undifferentiated spermatogonia is more likely a result of abnormal cell cycle or proliferation of progenitor cells.

In neonatal mice, the first round of spermatogenesis initiates directly from prospermatogonia to KIT⁺ differentiating spermatogonia, which continue to develop and produce the first wave of spermatozoa (Yoshida et al., 2006; Law et al., 2019). Meanwhile, another set of prospermatogonia become SSCs which are capable of self-renewal or differentiate into progenitors to initiate spermatogenesis and support the continuity of steady-state spermatogenesis (Yoshida et al., 2006). In P3 Srsf10-cKO testes, despite the drastic loss of SRSF10 protein, the number of MVH⁺ germ cells was comparable to that in control, suggesting that prospermatogonia can probably develop into KIT⁺ differentiating spermatogonia. However, the meiosis initiation was still impaired in the P8-P15 Srsf10-cKO testes during the first wave of spermatogenesis. This suggests that loss of SRSF10 might lead to developmental arrest of KIT⁺ differentiating spermatogonia or SRSF10 might be also involved in the initiation of meiosis. In 2-month-old Srsf10-cKO testes, differentiating spermatogonia cannot be detected, indicating that the inefficient expansion of PLZF⁺ undifferentiated spermatogonia may lead to failure of differentiation during the subsequent rounds of SSC-dependent spermatogenesis.

In the absence of SRSF10, it is interesting that a unique cluster of cells, the DSPG3 was only observed in the scRNA-seq data of the Srsf10-cKO group. These cells express the differentiated markers Stra8, Kit, and Sohlh1, but at a lower level than that in the DSPG1 and DSPG2. We speculate that these cells might be directly transited from the fetal prospermatogonia in the first round of spermatogonia (Yoshida et al., 2006), or a population of abnormally differentiated cells in the process of spermatogonia differentiation, but later cell cycle defects of these cells lead to developmental arrest.

As a splicing factor, SRSF10 depletion in spermatogonia affected the splicing of several hundreds of genes, among which were 113 genes that were directly bound by SRSF10 as detected by LACE-seq. These targets are involved in many fundamental biological processes, such as regulation of double-strand break repair, chromosome segregation, and mitotic spindle organization. Importantly, aberrant splicing of some functional genes can be successfully verified experimentally at both the mRNA and protein levels. For example, Nasp, which encodes a histone chaperone that preferentially transports H1 histones into nuclei and exchanges H1 histones with DNA (Richardson et al., 2006), preferentially skips exon 7 in the absence of SRSF10 in the spermatogonia. This leads to a dramatic decrease of the long isoform (also known as testicular NASP or tNASP; Richardson et al., 2000) and an increase of a shorter isoform. Notably, depletion of tNASP reportedly inhibits proliferation in prostate cancer PC-3 cells and renal cell carcinoma cells (Alekseev et al., 2011; Fang et al., 2015), echoing the cell cycle defects of Srsf10-cKO spermatogonia. Bclaf1 is a known target of SRSF10, and the inclusion of Bclaf1 exon5a was directly regulated by SRSF10 (Zhou et al., 2014a). In colorectal cancer cells, knockdown of the BCLAF1-L isoform (exon 5 a included) inhibited growth, and overexpression of the BCLAF1-L isoform increased tumorigenic potential (Zhou et al., 2014a). In Srsf10-cKO-enriched spermatogonia, the inclusion of Bclaf1 exon5a was decreased at both the RNA and protein levels, leading to downregulation of BCLAF1-L isoform and thus proliferation defects. Therefore, the negative effects on cell proliferation of Srsf10-depleted spermatogonia might be due to abnormal AS of abundant functional genes (Figure 8). However, how the aberrant splicing of these genes affects their functions in spermatogonia needs to be further clarified.

Besides the factors that are involved in fundamental cellular events, we found and verified the aberrant splicing of many genes that play critical roles in male germ cells, including Dazl, Kit, Ret, and Sycp1, in Srsf10-deficient spermatogonia (Figure 9). Although the functions of specific isoforms and the effects of isoform switches in these genes in spermatogonia are unclear at the moment, specific targets or functions of different isoforms are reported in other cell lines (Yoshinaga et al., 1991; Caruana et al., 1999; Crosier et al., 1993; Hofmann, 2008; Naughton et al., 2006; Parker et al., 2014). For example, the specific mRNA targets for both DAZL isoforms (the exon 8-included long isoform is increased in Srsf10-cKO testes) were identified in ESCs, implying the potential functional divergence of these two isoforms in spermatogenesis (Xu et al., 2013). We speculate that the splicing of these genes should be precisely regulated to keep the balance of their isoforms and exert normal functions in spermatogenesis. However, it should be noted that these genes are not directly bound by SRSF10, indicating that their abnormal splicing may be a secondary effect of Srsf10 depletion.

Interestingly, besides changes in gene splicing as expected, depletion of Srsf10 in spermatogonia leads to changes in gene expression, especially when lower the cutoff (378 upregulated and 206 downregulated). However, almost none of these genes were the direct targets of SRSF10 (24 genes in 1207 genes, 0.041% overlap), and nearly no DSEs were observed (27 genes in 675 genes, 4% overlap). Considering the altered cell types (e.g. the loss of progenitors and differentiating spermatogonia) and gene splicing in the absence of SRSF10, changes in gene expression might be regulated indirectly by SRSF10.

All mice were maintained under specific-pathogen-free conditions and the illumination time, temperature, and humidity were all in accord with the guidelines of the Institutional Animal Care and Use Committee of the Institute of Zoology at the Chinese Academy of Sciences (CAS; SYXK 2018–0021). The procedures for care and use of animals were approved by the Ethics Committee of the Institute of Zoology at the Chinese Academy of Sciences (IOZ20180083). The Srsf10^{Floxed/Floxed} (Srsf10^F/F) mice were purchased from Shanghai Model Organisms Center, Inc. The Srsf10^F/F male mice were mated with Vasa-Cre transgenic females to obtain the mouse model with Srsf10 specific deletion in the germ cell lines. The purchased Srsf10^F/F mice are on C57BL/6 J genetic background, while the Vasa-Cre mice are on a mixed background. Srsf10^F/+;Vasa-Cre males (the floxed allele in mature sperm will be deleted by Vasa-Cre and thus generate a knockout allele [‘-’]), and Srsf10^F/F females were used for breeding. Four genotypes in the progeny, including Srsf10^F/+, Srsf10^F/−, Srsf10^F/+;Vasa-Cre, and Srsf10^F/−;Vasa-Cre can be identified. The genotype of Srsf10^F/−;Vasa-Cre was used as mutants and was referred to as Srsf10-cKO. The genotypes of Srsf10^F/+;Vasa-Cre were used as control. Genotyping of Srsf10 was performed by PCR of mice tail genomic DNA. Forward primer: 5-AACATTTAGCACATTTGAGGAT-3, and reverse primer: 5-AACAGCCATATTAACCCGTCTTG-3 were used to detect the wild-type allele (615 bp) and the floxed allele (467 bp). Forward primer: 5-AGCATGCCTATCTTGTGT-3, and reverse primer: 5-TAACCCGTCTTGTAGTAAATCT-3 were used to detect the mutant allele (300 bp). The Vasa-Cre was genotyped with forward primer (5-CACGTGCAGCCGTTTAAGCCGCGT-3) and reverse primer (5-TTCCCATTCTAAACAACACCCTGAA-3) with the product was 240 bp. The annealing temperature of all primers was 58℃.

Each control and Srsf10-cKO male mice (8–12 weeks, n=8) were caged with two 8-week-old wild-type ICR females, and vaginal plugs were checked every morning. Once a vaginal plug was identified (day 1 postcoitus), the male was allowed to rest for 2 days. Two days later, another two females were placed in the cage for another round of mating until two to three plugged females for each male mouse were obtained. The plugged females were separated and monitored for their pregnancy. The fertility test lasted for at least 4 weeks.

For histological analysis, testes from control and Srsf10-cKO were isolated and fixed in Bouin’s solution (saturated picric acid: 37% formaldehyde:glacial acetic acid = 15:5:1) overnight at room temperature (RT). These testes were dehydrated through a graded ethanol (30, 50, 70, 80, 90, 100, and 100%) 1 hr for each step, xylene three times, 1 hr for each, paraffin (65°C), two changes, 2 hr each, and embedded testes in paraffin. Then, paraffin-embedded samples were cut into sections of 5 μm thickness. After dewaxing and hydration, the sections were stained with hematoxylin and 1% eosin and imaged with a Nikon ECLIPSE Ti microscope.

For immunostaining, testes from control and Srsf10-cKO mice were isolated and fixed in 4% PFA overnight at 4℃. Following dehydration, the testes were embedded in paraffin and cut into sections of 5 μm thickness. After dewaxing and hydration, the sections were boiled in citrate antigen retrieval solution (0.01 M citric acid/sodium citrate, pH 6.0) for 20 mins in the microwave oven. After free cooling, the sections were washed with PBS (pH 7.4) three times and blocked with 5% BSA in PBS for 1 hr at RT. Then, the sections were incubated with primary antibody diluted with 1% BSA overnight at 4℃. On the second day, we washed the sections with PBS three times and incubated them with the secondary antibody diluted with 1% BSA for 1 hr at RT.

After washing in PBS three times, the sections were incubated with 2 µg/ml of Hoechst 33342 (Sigma, B2261) diluted with PBS for 15 min at RT. Finally, the sections were washed with PBS two times and mounted with Fluoromount-G medium (Southern Biotech, 0100–01). The immunofluorescence staining was imaged with a laser scanning confocal microscope LSM880 (Carl Zeiss, Germany).

The primary antibodies used were listed as follows: rabbit anti-SRSF10 polyclonal antibody (ab254935, Abcam, 1:200); goat anti-PLZF polyclonal antibody (AF2944, R&D, 1:200); goat anti-KIT polyclonal antibody (AF1356, R&D, 1:200); goat anti-GFRα1 polyclonal antibody (AF560, R&D, 1:200); rabbit anti-DDX4/MVH polyclonal antibody (ab13840, Abcam, 1:200); rabbit anti-phospho-Histone H2A.X (Ser139/Tyr142) antibody (#5438, Cell Signaling Technology, 1:200); mouse anti-SCP3 antibody (mouse monoclonal) (ab97672, Abcam, 1:200); rabbit anti-Cleaved Caspase-3 (Asp175) antibody (#9661, Cell Signaling Technology, 1:200); and rabbit anti-Ki67 polyclonal antibody (ab15580, Abcam, 1:200).

The secondary antibodies used were listed as follows: Alexa Fluor 488 donkey anti-rabbit (Jackson, 1:500); Alexa Fluor 549 donkey anti-rabbit (Jackson, 1:500); Alexa Fluor 488 donkey anti-mouse (Jackson, 1:500); Alexa Fluor 549 donkey anti-mouse (Jackson, 1:500); and Alexa Fluor 488 donkey anti-goat (Jackson, 1:500).

Total RNA was extracted from whole testes or enriched cells using RNAzol RT (Molecular Research Center. Inc, RN 190) following the manufacturer’s instructions. After removing the residual genomic DNA with the DNase I Kit (Promega, M6101), 500 ng of total RNA was reverse-transcribed into cDNAs using the PrimeScript RT Reagent Kit (TaKaRa, RR037A) according to the manufacturer’s protocol. qRT-PCR was performed using an Eva Green 2× qPCR MasterMix-No Dye kit (Abm, MasterMix-S) on a LightCycler 480 instrument (Roche). Relative gene expression was analyzed based on the 2^−ΔΔCt method with β-actin as internal controls. At least three independent experiments were analyzed. All primers were listed in Supplementary file 1.

The protein from testes or enriched cells was extracted using Radio-Immunoprecipitation Assay (RIPA) lysis buffer (50 mM Tris–HCl (pH 7.5), 150 mM NaCl, 1% sodium deoxycholate, 1% Triton X-100, 0.1% Sodium dodecyl sulfate (SDS), 5 mM EDTA, 1 mM Na₃VO₄, and 5–10 mM NaF) containing a protease inhibitor cocktail (Roche, 04693132001), and the protein lysis buffers were incubated on ice for 20 min. After the ultrasound, the protein lysis buffers were centrifuged at 4°C, 12,000 rpm for 20 min, and quantified using a BCA reagent kit (Beyotime, P0012-1). After being boiled at 95°C for 6 min, equal amounts of total protein lysates were used for immunoblotting analysis. Different molecular weight proteins were separated in a 10% SDS–PAGE gel and transferred onto polyvinylidene fluoride (PVDF) membranes. After blocking with 5% non-fat milk dissolved with Tris Buffered Saline with Tween 20 (TBST, pH 7.4) for 1 hr at RT, the membranes were incubated with diluted primary antibodies diluted with 1% BSA at 4°C overnight. After three washes with TBST, the membranes were incubated with secondary antibodies diluted with TBST at RT for 1 hr. The signals were developed with Pierce ECL Substrate (Thermo Fisher Scientific, #34080), detected with Bio-RAD ChemiDocTMXRs+, and analyzed with Quantity One software (Bio-Rad Laboratories). All primary antibodies were listed as follows, rabbit anti-SRSF10 polyclonal antibody (NB110-93598, Novus Biologicals, 1:1,000); goat anti-PLZF polyclonal antibody (AF2944, R&D, 1:1,000); rabbit anti-DDX4/MVH polyclonal antibody (ab13840, Abcam, 1:1,000); rabbit anti-phospho-Histone H2A.X (Ser139/Tyr142) antibody (#5438, Cell Signaling Technology, 1:1,000); mouse anti-human DAZL monoclonal antibody (MCA23336, Bio-Rad, 1:500); BCLAF1 rabbit polyclonal antibody (26809–1-AP, Proteintech, 1:1000); NASP rabbit polyclonal antibody (11323–1-AP, Proteintech, 1:1000); and KAT7 rabbit polyclonal antibody (13751–1-AP, Proteintech, 1:1000).

The secondary antibodies used were listed as follows: Goat Anti-Rabbit IgG (H+L), HRP Conjugated (EASYBIO, BE0101, 1:3000); Goat Anti-Mouse IgG (H+L)-HRP Conjugated (EASYBIO, BE0102, 1:3000); Rabbit Anti-Goat IgG (H+L)-HRP Conjugated (ZSGB-BIO, ZB-2306, 1:3000).

The testes were collected and dissected to remove the tunica albuginea. Seminiferous tubules were dispersed with tweezers and fixed at 4% PFA overnight at 4 °C. The tubules were washed three times with PBST (pH 7.4) for 10 min each and permeated with 0.1% TritonX-100 for 4 h at RT. Then, the tubules were washed three times with PBST and blocked with 5% BSA in PBST for 2 h at RT. The tubules were incubated with primary antibodies diluted with 1% BSA at 4 °C overnight. After washing with PBST and the tubules were incubated with secondary antibodies diluted with PBST for 4 h at RT. With the washing of PBST, the tubules were stained with Hoechst diluted with PBST for 30 min at RT. After simply washing, the tubules were mounted with Fluoromount-G medium (Southern Biotech, 0100–01). The imaging of whole-mount staining followed the protocol described above.

Testes samples were collected from P3, P6, and P8 control and Srsf10-cKO mice. THY1⁺ spermatogonia were isolated from P6 control and Srsf10-cKO mice. The RNA-seq experiment was performed in two biological replications of P3, P6, and P8 testes and isolated THY1⁺ spermatogonia in control and Srsf10-cKO mice. Total RNA was isolated using the RNAzol RT (Molecular Research Center. Inc, RN 190) according to the manufacturer’s protocol and treated with DNase I to remove residual genomic DNA. A total amount of 1 μg of RNA per sample was used to prepare cDNA libraries generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (NEB) following the manufacturer’s instructions. 6 G base pairs (raw data) were generated by Illumina Novaseq 6000 for each cDNA library. The adaptor sequence and sequences with a high content of unknown bases or low-quality reads were removed to produce the clean reads used for bioinformatic analysis.

After initial quality control, the clean reads were aligned to the mouse reference genome (mm 9) using Tophat v2.1.1 (Trapnell et al., 2009). Next, the gene expression was calculated by Cufflinks v2.2.1. The normalization of gene expression values was based on theFPKM.

EdU (RiboBio, C00053) dissolved in PBS was injected intraperitoneally at 5 mg/kg of body weight. Testes were collected from control and Srsf10-cKO mice 4 hr later following EdU incorporation. For the EdU and PLZF co-staining, the testes were fixed in 4% PFA overnight at 4°C, embedded in paraffin, and then performed according to the protocol of Cell-Light Apollo567 Stain Kit (100T) (RiboBio, C10310-1). Briefly, paraffin-embedded samples were cut into sections of 5 μm thickness. After dewaxing and hydration, the sections were washed with 2 mg/ml glycine for 10 min, incubated with 0.5% TrionX-100 in PBS for 10 min, and then washed with PBS for 5 min. Next, the section was stained with fresh 1×Apollo reaction solution for 30 min at RT. The section was washed with 0.5% TrionX-100 three times for 10 min each time, washed with methanol two times for 5 min each time, and PBS two times for 5 min each. Then, the sections were blocked with 5% BSA in PBS for 1 hr at RT, incubated with primary antibody diluted with 1% BSA overnight at 4 ℃. On the second day, we washed the sections with PBS three times and incubated them with secondary antibody diluted with 1% BSA for 1 hr at RT. After washing in PBS three times, the sections were incubated with 2 µg/ml of Hoechst 33342 (Sigma, B2261) diluted with PBS for 15 min at RT. Finally, the sections were washed with PBS two times and mounted with Fluoromount-G medium (Southern Biotech, 0100–01). The immunofluorescence staining was imaged with a laser scanning confocal microscope LSM880 (Carl Zeiss, Germany).

Testes from P6 mice were used to generate single-cell suspensions following enzymatic digestion as described previously (Oatley and Brinster, 2006). In brief, testes were collected from P6 or P8 control and Srsf10-cKO mice in Hanks’ balanced salt solution, and the tunica albuginea was removed. Then, the testes were digested with 4.5 ml 0.25% trypsin/EDTA and 0.5 ml 7 mg/ml DNase I solution (Sigma, d5025) for 6 min at 37°C. After gently pipetting, another 0.5 ml DNase I solution was added to the cell suspension to digest for another 2–3 min at 37°C and followed by the addition of 1 ml 10% FBS. Single-cell suspensions were made by gently repeated pipetting and passed through a 40-μm pore size cell strainer. The cells are centrifugated at 600 g for 7 min at 4°C and resuspended with 180 μl running buffer (Miltenyi Biotec, 130-091-221) for MACS selection.

We added 20 μl THY1 antibody-conjugated microbeads (anti-mouse CD90.2 [Thy1.2] MicroBeads; Miltenyi Biotech, 130-121-278) to the single-cell suspensions and mixed well, then incubated for 20 min at 4°C. After incubation, 2 ml running buffer was added to the cells and centrifugated at 600 g for 7 min at 4°C. The pellet was then resuspended in 500 μl of running buffer for magnetic cell separation. The LS columns (Miltenyi Biotec, 130-042-401) were placed in the magnetic field of the MACS Separator and prewashed with 0.5 ml of running buffer followed by the addition of the THY1-labeled cell suspension. Wash the LS columns three times with 3 ml running buffer, and the unlabeled THY1⁻ cells were eluted. Then, the LS columns were removed from the separator and placed on new 15 ml centrifuge tubes. The THY1⁺ cells were eluted from the LS columns in a 5-ml running buffer and centrifuged at 600 g for 7 min at 4°C. After centrifugation, the supernatant is removed, and the pellet of THY1⁺ cells was stored at –80°C for subsequent sequencing analysis and validation.

THY1⁺ KIT^-, KIT⁺ THY1⁻, and THY1⁺KIT⁺ spermatogonia collection: Testes collected from P8 control and Srsf10-cKO mice were digested, and the single-cell suspensions were generated following the protocol described above. We added 20 μl THY1 antibody-conjugated microbeads (anti-mouse CD90 [Thy1.2] MicroBeads; Miltenyi Biotech, 130-121-278) and 40-μl KIT antibody-conjugated microbeads (anti-mouse CD117 MicroBeads; Miltenyi Biotech, 130-091-224) to the single-cell suspensions for 20 min at 4°C, and followed the protocol described above to get the THY1⁺ KIT⁻, KIT⁺ THY1⁻, and THY1⁺KIT⁺ spermatogonia.

The single-cell RNA-seq experiment was performed with one replicate of control that was collected from three mice, and two replications of Srsf10-cKO that were collected from six mice, respectively. Single cells were suspended in PBS containing 0.04% BSA and loaded onto the Chromium 3' v3 platform (10× Genomics) to generate single-cell libraries according to the manufacturer’s protocol. Briefly, single cells were partitioned into Gel Bead-In-EMulsions (GEMs) in the 10× Chromium Controller instrument followed by cell lysis and barcoded reverse transcription using a unique molecular identifier (UMI). The cDNA was generated and then amplified, and the libraries were finally sequenced using an Illumina Novaseq 6000 sequencer with a sequencing depth of at least 100,000 reads per cell with a pair-end 150 bp (PE150) reading strategy (performed by CapitalBio Technology, Beijing).

Raw data were processed using the Cell Ranger Software (version 4.0.0). Briefly, the raw files were converted to demultiplexed fastq files through the Cell Ranger mkfastq pipeline. The fastq files were then aligned to the mouse reference genome (mm 10) using the STAR aligner. Next, the reads were further filtered for valid cell barcodes and UMIs to produce a count matrix. Finally, the count matrix was imported into the R package Seurat, and quality control was performed to remove outlier cells and genes. Cells with 200–4000 detected genes were retained. Genes were retained in the data if they were expressed in ≥3 cells. After applying these quality control criteria, 1923 cells and 23,310 genes remained for further analysis. Additional normalization was performed in Seurat on the filtered matrix to obtain the normalized count. Highly variable genes across single cells were identified, and principal components analysis was performed to reduce the dimensionality. Then the top 16 principal components were used for cluster/subtype identification and UMAP visualization (Becht et al., 2018). Known cell type-specific markers were used to match each cell type.

Germ cell lineage trajectories were constructed according to the procedure recommended in the Monocle3 documentation (Trapnell et al., 2014, https://cole-trapnell-lab.github.io/monocle3/docs/starting/). Briefly, the top differentially expressed genes were selected as ‘ordering genes’ to recover lineage trajectories in Monocle3 using default parameters. After pseudotime was determined, differentially expressed genes were clustered to verify the fidelity of lineage trajectories.

SRSF10 LACE-seq was performed based on a previously described protocol with some modifications. Briefly, THY1⁺ cells were collected into 1.5 ml LoBind microcentrifuge tubes (Eppendorf, 022431021) with 5 µl of 1×PBS (pH 7.4). The cells were irradiated twice with 0.40 J cm−2 UV light (254 nm) in a CL-1000 ultraviolet crosslinker (UVP). 10 µl of protein A/G magnetic beads (per sample, Thermo Scientific, 26162) were washed twice with BSA/PBS solution (0.1% BSA in 1×PBS) and incubated with 200 µl blocking buffer (1×PBS, 0.2 mg/ml glycogen, 0.2 mg/ml BSA) at RT for 1 hr. The blocked beads were then washed once with 0.1 M Na-phosphate buffer (93.2 mM Na₂HPO₄, 6.8 mM NaH₂PO₄, 0.05% tween 20, pH 8.0) and then resuspended in 40 µl of 0.1 M Na-phosphate buffer containing 5 µg SRSF10 antibody (Cat No.) or IgG (Cat No.), incubating at RT for 1 hr. The antibody-coupled beads were washed twice with wash buffer (1×PBS, 0.1% SDS, 0.5% NP-40, 0.5% sodium deoxycholate) and resuspended in 10 µl of wash buffer per sample. The cross-linked samples were lysed on ice with 50 µl of wash buffer for 10 min. After removal of genomic DNA with 4 µl of RQ1 DNase (Promega, M6101) in the presence of 1 µl of RNase inhibitor (Thermo Scientific, EO0381), 10 µl of antibody-coupled beads were added to the lysate and incubated for 1 hr at 4°C. Bead-bound antibody-RNA complexes were then washed twice with wash buffer, once with high-salt wash buffer (5×PBS, 0.1% SDS, 0.5% NP-40, 0.5% sodium deoxycholate), and once with PNK buffer (50 mM Tris-HCl, pH 7.4, 10 mM MgCl₂, 0.5% NP-40). The immunoprecipitated RNAs were then fragmented with 1×10^–5 U of micrococcal nuclease (MNase, New England BioLabs, M0247S) in 1×MN reaction buffer (50 mM Tris-HCl, pH 8.0, 5 mM CaCl₂) for 3 min at 37°C. After another round of extensive washing (twice with 1×PNK + EGTA buffer [50 mM Tris-HCl, pH 7.4, 20 mM EGTA, 0.5% NP-40], twice with wash buffer, and twice with PNK buffer), the RNA 3’ ends were dephosphorylated on beads with FastAP alkaline phosphatase (Thermo Scientific, EF0651) for 15 min in FastAP buffer. After washing beads twice with 1×PNK + EGTA buffer, twice with 1×PNK buffer, and twice with BSA solution (0.2 mg/ml BSA in DEPC water), the 3’ linker was ligated with T4 RNA ligase 2 (New England BioLabs, M0242) for 2.5 hr at RT. After washing beads three times with 1×PNK buffer, the RNA was reverse transcribed with Superscript II reverse transcriptase (Thermo Scientific,18064014) according to the manufacturer’s instruction. Then excess T7-RT primer was digested with Exonuclease I (New England BioLabs, M0293), first-strand cDNA was released from Protein A/G beads by treatment with RNase H (Thermo Scientific, EN0202) and captured by streptavidin C1 beads (Thermo Scientific, 650002). After washing beads twice with 1×B & W buffer (5 mM Tris-HCl, pH 7.5, 0.5 mM EDTA, 1 M NaCl), once with BSA solution, the cDNA 3’ linker was ligated with T4 RNA ligase 1 (New England BioLabs, M0437) overnight at RT. Then cDNA was pre-amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems, KK2601), and PCR products were purified with Ampure XP beads (Beckman Coulter, A63881). Then in vitro transcription was performed, the DNA template was removed with TURBO DNase (Thermo Scientific, AM2238), and the RNA was purified with Agencourt RNA Clean beads (Beckman Coulter, A63987). After reverse transcription and indexed PCR, the PCR products were size-selected on a 2% agarose gel, and regions corresponding to 250–500 bp were purified using Gel Extraction Kit (Qiagen, 28604). The LACE-seq library was paired-end sequenced using Illumina NovaSeq 6000 at Novogene.

The first 4 nt at 5’ end of read1 and read2 were extracted as UMI and then the adaptor sequences, poly(A) tails at the 3’ end and low-quality reads were removed using fastp (Chen et al., 2018) with parameters ‘--detect_adapter_for_pe -m -e 20 l 18 -y -Y 10 c --overlap_len_require 10 --overlap_diff_percent_limit 10 U --umi_loc per_read --umi_len 4--poly_x_min_len 5’. Clean reads were then first mapped to mouse pre-rRNA using Bowtie2 software (v.2.1.0; Langmead and Salzberg, 2012), and the remaining unmapped reads were aligned to mouse mm9 genome using HISAT2 (Kim et al., 2015). PureCLIP (Krakau et al., 2017) was used to identify peaks with default parameters. For motif analysis, LACE-seq peaks were firstly extended 20 nt to the 5’ upstream, and the overrepresented hexamers were identified using the resultant peaks with Homer Heinz et al., 2010. The enrichment of mRNA in each sample was calculated using cufflinks 2.2.1 and expressed as FPKM.

THY1⁺ spermatogonia were isolated from P6 control and Srsf10-cKO mice. Total RNA was isolated using the RNAzol RT (Molecular Research Center. Inc, RN 190) according to the manufacturer’s protocol and treated with DNase I to remove residual genomic DNA. 5 μg of total RNA per sample was used to prepare the Iso-Seq library using the Clontech SMARTer cDNA synthesis kit and the BluePippin Size Selection System protocol as described by Pacific Biosciences (PN 100-092-800-03).

After running the Iso-Seq pipeline, sequence data were processed using the SMRTlink 5.0 software. A circular consensus sequence was generated from subread BAM files. Additional nucleotide errors in consensus reads were corrected using the Illumina RNAseq data with the software LoRDEC. Then all the consensus reads were aligned to the mouse reference genome (mm 9) using Hisat2.

Differential splicing events of Iso-seq data were analyzed using SUPPA2 software with the standard protocol. The SUPPA2 software can identify the seven common modes of AS events and obtain accurate splicing change quantification between control and Srsf10-cKO samples. We used p<0.05 and |ΔPSI |>0.1 as the threshold to filter for significantly differential splicing events. Differential splicing events of NGS data were analyzed using CASH software with the standard protocol using p<0.05 as the threshold for filtering. For validation, we first imported the differentially spliced sites of interesting functional genes analyzed by SUPPA2 and CASH into the integrative genomics viewer tool to efficiently and flexibly visualize and explore spliced sites between control and Srsf10-cKO samples. The primers for differentially spliced exons were designed using Primer5. Primers were designed within constitutive exons flanking the differentially spliced exons. Standard PCR for analysis by gel electrophoresis was performed according to the manufacturers’ instructions and visualized by running on a 2% agarose gel. All primers were listed in Supplementary file 2.

All experiments were performed at least three independent times. At least three independent biological samples were collected for the quantitative experiments. Quantification of positively stained cells was counted from at least three independent fields of view. Paired two-tailed Student’s t-test was used for statistical analysis, and data were presented as mean ± SEM. *** represent p<0.001, ** represent p<0.01, and * represent p<0.05. p<0.05 was considered with a significant difference level. Equal variances were not formally tested. No statistical method was used to predetermine sample sizes.

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

We thank Dr. Wei Xie's lab from Tsinghua University for computational facility assistance. We thank Dr. Eugene Yujun Xu from Nanjing Medical University for kindly providing anti-DAZL antibody. We thank Chengpeng Xu, Shiwen Li and Xili Zhu for their technical assistance. Jian Chen and all members of Sun lab for their helpful advice. We thank Mingming Fan for her guidance on MACS of spermatogonia. This study was funded by the National R & D Program (2018YFA0107701), National Natural Science Foundation of China (31801241, 31801240, 81971452, 81871211), the Natural Science Foundation of Guangdong Province, China (Grant No. 2018A030313665 and 2021 A1515011011), and the Medical Key Discipline of Guangzhou (2021–2023).

All mice were maintained under specific-pathogen-free (SPF) conditions and the illumination time, temperature and humidity were all in accord with the guidelines of the Institutional Animal Care and Use Committee of the Institute of Zoology at the Chinese Academy of Sciences (CAS; SYXK 2018-0021). The procedures for the care and use of animals were approved by the Ethics Committee of the Institute of Zoology at the Chinese Academy of Sciences (IOZ20180083).

© 2022, Liu, Lu, Zhao et al.

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