|Home | About | Journals | Submit | Contact Us | Français|
The agouti-yellow (Ay) deletion is the only genetic modifier known to suppress testicular germ cell tumor (TGCT) susceptibility in mice or humans. The Ay mutation deletes Raly and Eif2s2, and induces the ectopic expression of agouti, all of which are potential TGCT-modifying mutations. Here we report that the reduced TGCT incidence of heterozygous Ay males and the recessive embryonic lethality of Ay are caused by the deletion of Eif2s2, the beta subunit of translation initiation factor eIF2. We found that the incidence of affected males was reduced 2-fold in mice that were partially deficient for Eif2s2 and that embryonic lethality occurred near the time of implantation in mice that were fully deficient for Eif2s2. In contrast, neither reduced expression of Raly in gene-trap mice nor ectopic expression of agouti in transgenic or viable-yellow (Avy) mutants affected TGCT incidence or embryonic viability. In addition, we provide evidence that partial deficiency of Eif2s2 attenuated germ cell proliferation and differentiation, both of which are important to TGCT formation. These results show that germ cell development and TGCT pathogenesis are sensitive to the availability of the eIF2 translation initiation complex and to changes in the rate of translation.
The agouti-yellow (Ay) mutation is one of the original mutants inherited from mouse fanciers at the beginning of genetics a century ago. Ay achieved notoriety because its inheritance was an apparent violation of Mendel's law of segregation (1,2). The Ay mutation deletes Raly (a member of the hnRNP RNA-binding protein family) and Eif2s2 (the beta subunit of translation initiation factor eIF2), and also causes the ectopic expression of agouti (a melanocortin receptor antagonist) (Fig. 1A) (3,4). Ay produces remarkably diverse phenotypes. Ectopic expression of agouti and the resulting chronic inhibition of melanocortin receptor signaling causes dominantly inherited yellow fur, obesity, type II diabetes and susceptibility to somatic tumors (4–8). Loss of Raly expression has been implicated in the embryonic lethality of homozygous Ay mice (3,4,9). Interestingly, deletion of Eif2s2 in agouti-yellow mice has not been associated with an Ay phenotype, which is surprising considering the central role of eIF2 in regulating the global rate of translation initiation (10), the link between translation efficiency and tumorigenesis (11–13), and the lethal phenotype of eIF2 subunit mutations in yeast (14–16).
The Ay mutation is also the only known suppressor of susceptibility to spontaneous testicular germ cell tumors (TGCTs) when congenic on the 129 inbred background (17,18). TGCTs occur at an appreciable frequency only in the 129 family of inbred strains of mice (19). These TGCTs are strikingly similar to human pediatric testicular teratomas and teratocarcinomas, and arise during embryogenesis from primordial germ cells (PGCs), the precursors of sperm and eggs (20–24). As in humans, the genetic component of TGCT susceptibility in mice is strong but highly complex (18,19,25–28). In humans, the gr/gr deletion on the Y chromosome is the only variant that reproducibly associates with TGCT (27,28). In mice, targeted deficiency of Pten is the only mutation that increases susceptibility on all genetic backgrounds that have been tested (29). In addition, several single-gene mutations that modify TGCT susceptibility when congenic on the 129 inbred background have been useful in defining pathways that contribute to TGCT pathogenesis (30–34). Therefore, characterizing the gene at the agouti locus that modulates TGCT risk in mice is the first step towards identifying the cellular pathways that reduce TGCT susceptibility in mice and humans.
In the present study, we undertook a systematic series of tests including gene expression analyses and tumor surveys to determine which of the three candidate genes involved in the Ay mutation reduces TGCT susceptibility. We found that reduced expression of Eif2s2 suppresses TGCT susceptibility and influences the proliferation and differentiation of TGCT susceptible germ cells. In contrast, reduced expression of Raly and ectopic expression of agouti did not affect the frequency of affected males. Furthermore, in the process of identifying the TGCT-suppressing mutation, we also discovered that embryonic lethality of homozygous Ay mice results from loss of Eif2s2 expression.
We first sought to verify previous studies that showed TGCT incidence is significantly reduced in 129-Ay/+ males (17,19). However, the low incidence of TGCTs in wild-type 129 males means that large numbers of mice must be screened to test for reduced susceptibility. To enable a more statistically powerful test, Ay was bred onto the 129-Chr19MOLF (M19) chromosome substitution strain background, in which both copies of chromosome 19 are derived from the wild-derived MOLF/Ei inbred strain (35). Because homosomic M19 has a TGCT incidence of ~80%, tests for reduced susceptibility are relatively easy in a modest number of mice. A previous survey of M19-Ay/+ congenic consomic males showed that the Ay mutation significantly reduces the frequency of spontaneous TGCTs in M19 males (31). We increased the sample size of this survey, which now demonstrates that the Ay mutation reduces TGCT incidence in M19 males by 24% (Table 1). Therefore, because of these statistical advantages, subsequent studies to identify the TGCT-suppressing mutation in Ay mice were carried out using the M19 genetic background.
As a first step towards identifying the TGCT-suppressing mutation in Ay mice, we determined whether the three candidate genes are expressed in the testis during the correct developmental period. In mice, TGCTs arise from PGCs during a critical developmental window between embryonic days 11.5 and 13.5 (E11.5 to E13.5), and become evident microscopically as foci of embryonal carcinoma tumor stem cells at E15.5 to E16.5 (21,36). Currently, it is unknown whether TGCT susceptibility results from dysfunctions in PGCs, supporting somatic cells, or both. Thus, changes in candidate gene expression in one of several cell lineages during the period of susceptibility may influence TGCT incidence.
Eif2s2 and Raly were strongly expressed in the M19 embryonic testis at the time of TGCT initiation (Fig. 2). In contrast, agouti was expressed at minimally detectable levels in the M19 embryonic testis, as was observed in the adult M19 testis (Fig. 2C and Supplementary Material, Fig. S4B) (3). Analysis of wild-type embryonic testes that were FACS-sorted with a germ cell-specific Oct4ΔPE:GFP transgene (37) detected Raly and Eif2s2 in both PGCs and somatic cells (Supplementary Material, Fig. S1). In contrast, agouti, including a testis-specific splice variant (3), was detectable at minimal levels only in the somatic cells of the M19 embryonic testis (Supplementary Material, Fig. S2). We then tested whether the Ay mutation affected the expression of the candidate genes. The Ay deletion of Eif2s2 and Raly significantly reduced expression of both genes in the embryonic testis at the time of TGCT initiation (Fig. 2A and B). Furthermore, the Ay mutation significantly increased agouti expression in both PGCs and somatic cells (Fig. 2C and Supplementary Material, Fig. S2). Because Eif2s2, Raly and agouti are expressed in the fetal testis and because Ay alters their expression, all three genes qualify as candidate TGCT modifiers.
The next test sought to determine whether partial deficiency of Eif2s2 or Raly, in the absence of ectopic agouti expression, suppresses TGCT incidence. 129/Sv embryonic stem cell lines harboring 5′ untranslated region (5′-UTR) gene-trap alleles of Eif2s2 (Eif2s2Trap) or Raly (RalyTrap) were identified, and were independently bred onto the M19 genetic background (Supplementary Material, Fig. S3A–D). M19 mice heterozygous for Efi2s2Trap (Eif2s2Trap/+) or RalyTrap (RalyTrap/+) were viable, fertile and showed no gross abnormal phenotypes other than TGCTs. In both Eif2s2Trap/+ and RalyTrap/+ embryonic testes and adult tissues, expression of the targeted gene was reduced to the levels detected in Ay/+ embryonic and adult tissues (Fig. 2A and B and Supplementary Material, Fig. S3E and F).
The TGCT surveys of M19-Eif2s2Trap/+ and M19-RalyTrap/+ mice produced interesting results. The TGCT incidence in M19-Eif2s2Trap/+ mice was significantly reduced 2-fold compared with wild-type M19 siblings (Table 1). This decrease in TGCT susceptibility was similar to the previously reported reduction in TGCT incidence in M19-Ay/+ mice (31). In contrast, a survey of M19-RalyTrap/+ mice and M19 siblings showed that reduced expression of Raly did not reduce TGCT incidence (Table 1). Therefore, reduced expression of Eif2s2, but not Raly, acts as a TGCT suppressor in agouti-yellow mice.
To test whether the ectopic expression of agouti also influences TGCT susceptibility, we bred a ubiquitously expressed agouti transgene onto the M19 background (Supplementary Material, Fig. S4A). Compared with expression in wild-type M19 embryonic testes, agouti was strongly expressed in hemizygous transgenic embryonic testes, in both somatic cells and PGCs, at the time of TGCT initiation (Fig. 2C and Supplementary Material, Fig. S2). Furthermore, the agouti transgene was expressed in all adult tissues assayed (including the testis) and resulted in yellowing of the fur and a significant increase in body weight compared with wild-type siblings (Supplementary Material, Fig. S4B–D). Importantly, despite reproducing these dominant Ay phenotypes and inducing agouti expression in the fetal and adult testis, the transgene failed to reduce TGCT susceptibility in M19 mice (Table 1).
As a second test of the influence of agouti on TGCT susceptibility, we transferred the viable yellow (Avy) mutation onto the M19 background. Avy results from an intracisternal A particle (IAP) insertion in pseudo-exon 1A of agouti (Fig. 1B) (38). Cryptic promoters or enhancers in the long terminal repeats of the IAP drive ubiquitous expression of agouti without affecting Raly or Eif2s2, and thereby produce phenotypes similar to those of Ay/+ mice (8). Expression of agouti was significantly increased in Avy/+ embryonic testes, in both somatic cells and PGCs, at the time of TGCT initiation (Fig. 2C and Supplementary Material, Fig. S2). Additionally, the Avy mutation did not alter expression of Raly and Eif2s2 in the embryonic testis (Fig. 2A and B). As with the agouti transgene, the Avy mutation failed to reduce TGCT susceptibility in M19-Avy/+ or 129-Avy/+ males (Table 1 and Supplementary Material, Table S1).
We next tested whether variable levels of agouti expression in Avy/+ mice influence TGCT susceptibility. Promoter activity of the Avy IAP varies due to incomplete erasure of epigenetic modifications in the maternal germ line (39,40), resulting in a continuum of agouti expression and variable phenotype expressivity in isogenic Avy mice (38). Therefore, if agouti influences TGCT susceptibility, tumor incidence may be correlated with promoter activity and agouti expression levels. Coat color can be used as a proxy for promoter activity of the Avy IAP. Yellow mice have IAP activity in all cells, mottled-yellow mice are mosaics of cells with or without IAP activity, and agouti-like mice have an inactive IAP promoter in most cells (41). TGCT incidence was similar in yellow, mottled-yellow and agouti-like M19-Avy/+ and 129-Avy/+ mice (Supplementary Material, Table S2). The effect of IAP silencing extended to the Avy/+ embryonic testis, with expression varying over a 5-fold range and with one sample having almost undetectable levels of agouti expression (Fig. 2C). These results demonstrate that agouti expressivity did not affect TGCT susceptibility. Together, the results from the TGCT surveys of Eif2s2 gene-trap, Raly gene-trap, agouti transgenic and Avy mice support the conclusion that reduced expression of Eif2s2 acts as the TGCT suppressor in agouti-yellow mice.
For many TGCT modifiers, tumor susceptibility is elevated in heterozygotes and higher still in homozygous mutant males, but for other modifiers homozygosity causes embryonic lethality (19,33–35,42). Previous in vitro and genomic-based studies suggested that deletion of Raly causes the embryonic lethality of Ay/Ay mice (4,9). However, at the time of those studies, presence of Eif2s2 within the Ay deletion interval was not known and the contribution of Eif2s2 deficiency to embryonic development was not evaluated. Therefore, to test whether homozygosity for Eif2s2Trap further reduces TGCT susceptibility or causes lethality, Eif2s2Trap/+ mice were intercrossed to produce Eif2s2Trap/Eif2s2Trap offspring. Interestingly, these intercrosses failed to produce homozygous progeny, demonstrating that the loss of Eif2s2 expression was lethal (Table 2). In contrast, homozygous Raly gene-trap offspring were viable and present at the expected Mendelian frequency (Table 2).
Homozygous Ay mice die near the time of implantation, which is in part determined by genetic background (43). Therefore, we monitored Eif2s2 gene-trap intercross progeny from birth to weaning and did not observe lethality. Additionally, a small decrease in intercrosses litter size was observed when compared with backcross litters (Supplementary Material, Table S3). These observations are consistent with an embryonic lethal phenotype. To determine whether Eif2s2Trap/Eif2s2Trap embryos are lost near the time of implantation, E8.5 embryos from heterozygous intercrosses were genotyped. At E8.5, wild-type and heterozygous embryos were present at the expected Mendelian frequency for an intercross, but no homozygotes were found (Table 2). Additionally, approximately one-quarter of decidual swellings were empty, the majority of these probably corresponded to implantations of Eif2s2Trap/Eif2s2Trap embryos that induced a decidual response but failed to develop into gastrulated embryos (Table 2). These observations are consistent with those for other mutations that cause peri-implantation lethality (44,45). These findings show that loss of Eif2s2 expression leads to the embryonic lethality of Ay/Ay mice. Furthermore, with evidence from yeast showing that each of the three eIF2 subunits is essential for cell viability (14–16), these results demonstrate that the function of eIF2 during translation initiation is essential for viability among diverse eukaryotes.
Eif2s2 functions as one of the three subunits of eIF2, which is involved in one of the most tightly regulated steps in translation initiation (10). In response to stress, the availability of active eIF2 for translation initiation is reduced, which in turn decreases the global rate of protein synthesis (46). Modulating eIF2 availability controls cell division and survival, and increased eIF2 activity induces neoplastic transformation in vitro and is associated with several cancers in vivo (11,12). Conversely, several putative anti-cancer agents, which target the various regulatory steps of translation, including the availability of eIF2, decrease the rate of translation and inhibit tumor formation by inducing apoptosis or blocking cell cycle progression (47–50). Similarly, deficiency of eIF2 subunits likely decreases the availability of active eIF2 complexes and reduces the rate of translation initiation, which could act as a suppressor of tumorigenic potential.
Stevens and others proposed that TGCTs in 129/Sv mice arise from PGCs that continue to divide instead of entering mitotic arrest, which normally occurs around E13.5 (17). We therefore tested whether partial deficiency of Eif2s2 reduces TGCT incidence by decreasing proliferation, inducing apoptosis, or inhibiting the differentiation of germ cells after E13.5. To test whether the Eif2s2 gene-trap influences PGC proliferative capacity, we immunostained embryonic testis sections for phospho-Histone H3, a nuclear marker of mitotic cells (51). Interestingly, no significant difference in the percentage of proliferating PGCs was detected between M19 and M19-Eif2s2Trap/+ testes from E13.5 to E15.5 (Fig. 3A). However, at E16.5 the percentage of proliferating PGCs was significantly reduced in M19-Eif2s2Trap/+ testes compared with those from M19 control embryos (Fig. 3A–C). These findings are similar to a previous study of 129-Ay/+ embryonic testes, which demonstrated that the Ay mutation does not reduce the number of aberrantly proliferating PGCs until E16.5 (17). Thus, partial deficiency of Eif2s2 accounts for the reduced TGCT incidence and aberrant PGC proliferation in Ay males.
Chronic suppression of eIF2 activity induces apoptosis under certain cellular conditions (52). Therefore, we immunostained embryonic testis sections for cleaved caspase 3, a key mediator of programmed cell death (53), to test whether Eif2s2-deficiency influences the survival of aberrantly proliferating PGCs. Interestingly, apoptotic PGCs were rare in both M19-Eif2s2Trap/+ and M19 fetal testes, and a difference in the percentage of apoptotic PGCs was not observed from E13.5 to E16.5 (Fig. 3D). Taken together, these proliferation and apoptosis assays demonstrate that partial deficiency of Eif2s2 influences the mitotic activity but not the survival of PGCs.
Interestingly, the effect of the Eif2s2 gene-trap on PGC proliferation was restricted to a subset of cells. PGCs actively proliferate during development, expanding from a population of a few dozen cells at E7.5 to 25 000 cells at E13.5 (54). If reduced Eif2s2 expression influenced the proliferative capacity of the entire PGC population, then the total number of PGCs in the Eif2s2Trap/+ embryonic testis should be reduced compared with wild-type controls by E13.5. However, total germ cell numbers were similar between M19 and M19-Eif2s2Trap/+ embryonic testes at E14.5 and E16.5 (Fig. 3E). Therefore, the effect of reduced Eif2s2 expression on PGC proliferation appears to be restricted to the small population of aberrantly proliferating PGCs at a specific developmental time-point.
Reduced expression of Eif2s2 also affected adult germ cell development. Adult testis weight is often used as an indirect measure of alterations in germ cell numbers (55) and reduced fertility is an established TGCT risk factor (56,57). Interestingly, we observed a small but significant decrease in M19-Eif2s2Trap/+ testis weight compared with M19 controls at 6 weeks of age (Fig. 4A). Reductions in the spermatogonial stem cell pool can often lead to reduced germ cell numbers in the adult testis. However, comparison of testes from 1-day-old (P1) M19 and M19-Eif2s2Trap/+ neonates showed that the gene-trap did not reduce the initial spermatogonial stem cell population (Fig. 3E). Additionally, we did not observe significant defects in spermatogenesis in the adult gene-trap testes when compared with M19 controls (Fig. 4B and C). These results suggest that reduced Eif2s2 expression impeded but did not repress adult germ cell maturation.
An adult germ cell phenotype similar to that of mice partially deficient for Eif2s2 was reported for mice partially deficient for Eif2s3 (eIF2-gamma) (58). In mice, Eif2s3 is encoded on the short arm of the Y chromosome (Eif2s3y) and the X chromosome (Eif2s3x) (59). The Sxrb Y chromosome deletion of Eif2s3y causes a defect in spermatogonial proliferation and differentiation at several important stages of spermatogenesis, resulting in reduced numbers of meiotic spermatocytes and infertility (55,58). Additionally, Eif2s3y is one of a several genes known to escapes X inactivation, indicating that Eif2s3 gene dosage is critical in both sexes (59). Together with our results, these observations indicate that eIF2 subunit gene dosage is vital for proper maintenance of the germ cell lineage.
A systematic series of tests including gene expression analyses and tumor surveys revealed that reduced expression of Eif2s2 is the TGCT suppressor in agouti-yellow mice. Reduced Eif2s2 expression in gene-trap mice decreased TGCT incidence by 2-fold. Furthermore, reduced Eif2s2 expression decreased the number of aberrantly proliferating PGCs at E16.5 in TGCT susceptible testes and impaired adult spermatogenesis. In contrast, neither reduced expression of Raly in gene-trap mice nor ectopic expression of agouti in Avy or agouti transgenic mice suppressed TGCT susceptibility. Importantly, this is the first dominant Ay phenotype to be associated with the deletion of Eif2s2 and the only TGCT suppressing mutation to be characterized in humans and mice. Surprisingly, homozygosity for the Eif2s2 but not the Raly gene-trap resulted in embryonic lethality. As with Ay/Ay mice, death of Eif2s2 homozygous gene-trap mice occurred around the time of implantation, demonstrating that the loss of Eif2s2 expression accounts for the recessive embryonic lethality of Ay.
It remains to be determined how reduced expression of Efi2s2 suppresses TGCT susceptibility. However, changes in translation efficiency are a common feature of tumorigenesis (11,60). Several oncogenes and cell cycle regulators, including c-Myc, p27 and cyclin D1, have complex 5′-UTR secondary structures and require highly efficient translation initiation to maintain their expression (11,12,61). Activation of translation also suppresses expression of pro-apoptotic proteins (11). Not surprisingly, it has been proposed that increased translation rates promote tumor progression by maintaining proliferation, suppressing apoptosis and promoting pluripotency (12,13). In vitro studies support these hypotheses and implicate a role for increased eIF2 availability in proliferation, survival and neoplastic transformation (11,12). Conversely, decreased eIF2 availability likely prevents these processes. In the TGCT susceptible testis, our results suggest that reduced Eif2s2 expression suppresses proliferation and ultimately transformation.
The defects in adult male germ cell development in mice partially deficient for Eif2s2 and Eif2s3 may provide clues to the effect of reduced Eif2s2 expression on PGC development and TGCT pathogenesis. Differentiation from a spermatogonial stem cell to a meiotically committed Type B spermatagonia requires several concomitant mitotic divisions, which are intricately associated with germ cell differentiation (62). These division and differentiation steps appear to be sensitive to gene dosage effects of eIF2 subunits. In a similar manner, a reduction in the availability of eIF2 may attenuate the ability of aberrantly proliferating PGCs to obtain the self-renewal capacity and pluripotency of TGCT stem cells (63). In fact, we observed an effect on self-renewal in our proliferation assays. Eif2s2-deficency did not reduce the number of aberrantly proliferating PGCs until E16.5, a developmental time point at which TGCT foci have already begun to form (21,36). It is intriguing to speculate that the reduced number of proliferating PGCs observed in Eif2s2-deficient, E16.5 gonads resulted from blocking the acquisition of self-renewal capacity in the aberrantly proliferating PGC population. As observed in TGCT-resistant germ cells, the few remaining aberrantly proliferating PGCs in the majority of Eif2s2 gene-trap testes likely entered mitotic arrest (63).
Interestingly, Eif2s2 is not the only TGCT modifier that regulates translation. We previously identified a nonsense point mutation in Dead end 1 (Dnd1) as the cause for germ cell loss and increased TGCT susceptibility in 129/Sv-Ter mutant mice (33). Dnd1 has significant sequence similarity to the RNA-binding subunit (Acf) of the RNA editing complex and has been shown to block miRNA access to 3′-UTRs of transcripts involved in PGC development (Nanos1) and cell cycle regulation (Cdkn1b) (33,64). Argonaute or Piwi proteins associated with miRNAs in the RNA-induced silencing complex (miRISC) bind to 3′-UTRs of target transcripts (65). This complex inhibits translation by associating with the 5′cap of mRNAs and blocking assembly of the cap-binding complex (65). Interestingly, the Dnd1Ter mutation and the Ay deletion of Eif2s2 interact to modulate TGCT susceptibility (32), which implies that 5′cap and 3′-UTR regulation of translation are both important to the development of the PGC lineage and the pathogenesis of TGCTs.
129S1/SvImJ (129/Sv) (002448), C57BL/6J-Ay/+ (000021) and C57BL/6J-Avy/+ (000017) were obtained from the Jackson Laboratory (Bar Harbor, ME, USA). 129S1/SvImJ mice homozygous for the Oct4ΔPE:GFP transgene (33) and homosomic for the Chr19MOLF chromosome substitution (35) were obtained from our research colony. The Ay and Avy mutations as well as the Oct4ΔPE:GFP transgene were backcrossed for at least 10 generations onto 129/Sv to establish congenic strains and were then transferred with crosses to the M19 genetic background (See Supplementary Material, Table S4 for genotyping primer sequences). All protocols were approved by the CWRU Institutional Animal Care and Use Committee.
An agouti cDNA transgene driven by the human beta-actin promoter (pBAP-a) was modified to contain the loxP-flanked neomycin resistance cassette from pL452 (Supplementary Material, Fig. S4A) (6,66). The transgenic construct was introduced by electroporation into R1 ES cells, a hybrid of 129X1/SvJ and 129S1/Sv. G418 selection and quantitative real-time PCR (Q-PCR) were used to identify transgenic clones. BayGenomics ES cell clones RST374 and XH413 (derived from the 129P2/OlaHsd ES cell line E14Tg2a.4) were identified to have insertions in the second intron of Raly and the first intron of Eif2s2, respectively. Both inserted 5′ of the open reading frames and sequencing verified proper splicing of gene-trap sequences to 5′-UTR exons. The reverse transcriptase–PCR (RT–PCR) analysis of ES cell RNA verified proper splicing of the gene-traps to exon 2 of Raly and exon 1 of Eif2s2, respectively (Supplementary Material, Fig. S3A–C). ES cells were injected into C57BL/6J blastocysts using standard procedures to produce chimeras and the agouti transgene and gene-traps were transferred with crosses onto M19 background (see Supplementary Material, Table S5 for RT–PCR primer sequences).
Yellow fur and light pigmentation of the tail were used to distinguish Ay/+, Avy/+ and agouti transgenic mice from their wild-type siblings (56). PCR genotyping was used to identify Avy, agouti transgenic and gene-trap mice and embryos. RT–PCR genotyping of liver tissue was used to identify Ay embryos (See Supplementary Material, Table S4 for genotyping primer sequences).
Embryonic day 0.5 (E0.5) was assumed to be noon of the day the vaginal plug was observed. On the morning of the desired embryonic day, pregnant females were euthanized by cervical dislocation and embryos removed from the uterus in ice-cold 1xPBS. Embryos older than E14.5 were decapitated prior to dissection and gonads were removed in ice-cold 1xPBS. Tissues were collected and processed for specific assays and genotyping. PCR genotyping for Sry identified the sex of E12.5 embryos (Supplementary Material, Table S4). Gonad morphology identified the sex of E13.5–E16.5 embryos.
Crosses between M19 and M19-agouti mutant, transgenic or gene-trap mice, in both parental directions, were used to produce embryos for gonad dissections. Embryonic testes were lysed and RNA was prepared using the RNeasy Micro Kit (Qiagen). Adult tissues were collected and stored at −20°C in RNAlater (Ambion). RNA from adult tissues was collected by TriReagent extraction. RNA, 500 ng, was reverse transcribed with the SuperScript First-Strand Synthesis System. Q-PCR for agouti, Raly and Eif2s2 expression was performed with the Chromo4 real-time PCR system (MJ Research) and the PerfeCTa SYBR Green Supermix kit (VWR Scientific) using manufacturer-suggested protocols. Expression of agouti, Raly and Eif2s2 was normalized to the ubiquitously expressed housekeeping gene Rpl7 (67). Serial dilutions of wild-type (Raly and Eif2s2 expression analysis) or Avy (agouti expression analysis) adult testis cDNA were used to generate standard curves for each primer set. Significant differences in expression were tested by one-way ANOVA with the Bonferroni post-test for pair-wise comparisons (see Supplementary Material, Table S5 for Q-PCR primer sequences).
M19-Oct4ΔPE:GFP females were bred to M19-agouti mutant, transgenic or gene-trap males to produce embryos for gonad dissections. Single-cell suspensions of embryonic testes were generated as previously described (68). Gonads were digested in 0.25% trypsin (Invitrogen) for 15 min at 37°C. Tissues were triturated into single-cell suspensions and filtered through a 40 mm nylon mesh cell strainer (BD Falcon). The mesh was washed with 2% BSA in 1xPBS and the cells were kept on ice until FACS with the BD Biosciences FACSAria system. The Oct4ΔPE:GFP transgene was used to sort GFP-positive PGCs from GFP-negative somatic cells, which typically yielded 1500 to 3000 GFP-positive germ cells (98% purity) from both gonads of a single embryo (Supplementary Material, Fig. S2A) (68). Sorted cells were lysed and then RNA was prepared and reverse transcribed using the protocols described for embryonic testes. cDNA samples were PCR-amplified for 35 cycles for the appropriate genes (see Supplementary Material, Table S5 for RT–PCR primer sequences).
Crosses between wild-type and Avy, agoutiTg/−, RalyTrap/+ or Eif2s2Trap/+, in both parental directions, were used for the TGCT surveys. Male offspring were necropsied at 4–6 weeks of age and testes were visually examined for tumors, which are readily detected at these ages (31,35). Chi-square contingency tests were used to test for statistical differences between the number of affected control and experimental mutant or transgenic progeny. Finally, Avy males were sub-categorized by coat color, and chi-square contingency tests were used to test for statistical differences in TGCT incidence between coat color categories.
M19-Eif2s2Trap/+ females were bred to M19-Oct4ΔPE:GFP males for timed-matings. On the appropriate day, embryonic or neonatal testes were dissected and fixed overnight at 4°C in 4% paraformaldehyde. Samples were cryopreserved in 30% sucrose in 1xPBS and embedded in O.C.T. compound (Tissue Tek). Samples were sectioned (10 µm) and blocked in 5% goat serum and 3% BSA with PBS. Sections were incubated overnight at 4°C in blocking solution containing 1:200 diluted rabbit polyclonal anti-phospho-Histone H3 (Ser 10) (06-570, Upstate) or 1:200 diluted rabbit polyclonal anti-cleaved Caspase-3 (Asp175) (9661, Cell Signaling), washed with PBS, and incubated for 3 h at room temperature with goat anti-rabbit AlexaFluor 633 secondary antibody (A21701, Invitrogen) diluted 1:400 in blocking solution. Nuclei were counter-stained with DAPI. GFP-positive germ cells were counted using the Volocity (Version 4) software suite; antibody stained germ cells were counted blind to embryo genotype in three to four sections spaced 20–40 µm apart. Germ cells per tubule cross-section were calculated from 4 sections, 5–20 tubules/section, spaced 40 µM apart. Significant differences in antibody labeled cells and germ cells per tubule were tested by unpaired t-tests. For histology sections, adult tissues were fixed in 10% buffered formalin, sectioned (5 µm) and stained with hematoxylin and eosin.
Body weight of M19, M19-agoutiTg/− and M19-Ay/+ male mice was measured every 2–4 weeks (±3 days). From weaning until 12 weeks of age, mice were fed Lab Diet 5010 ad libitum. Following weighing at 12 weeks, M19 and M19-agoutiTg/− mice were fed a high fat, high sucrose diet (Research Diets D12331) ad libitum to accelerate differences in weight gain (6). M19 and M19-Eif2s2Trap/+ testis, without TGCTs, were weighed at 6-weeks of age. Significant differences in body and testis weight were tested using unpaired t-tests and P-values. Body weight P-values were corrected for multiple testing (five tests).
To identify the integration site of the XH413 gene-trap, a primer walking and sequencing strategy was utilized (34). Forward primers were designed to anneal to sequences at 500 bp intervals across Eif2s2 intron 1 and individually paired in PCR reactions with a reverse primer, 5′-GTTATCGATCTGCGATCTGCG-3′, which anneals to sequences ~1500 bp within the pGT1Lxf gene-trap vector. PCR of Eif2s2Trap/+ DNA produced a 2 Kb product using forward primer 5′-CAGCTGTGGTGTTCTGTGGT-3′. Sequencing of this PCR product with primer 5′-TCACAAGGCGTTTATGGTC-3′ (within the amplified Eif2s2 sequence) identified the gene-trap insertion site of ES cell line XH413 (Supplementary Material, Fig. S3D).
M19-RalyTrap/+ or M19-Eif2s2Trap/+ were intercrossed and weaning-age mice or E8.5 embryos were genotyped for gene-trap copy number. A Taqman Q-PCR assay for the gene-trap β-galactosidase/neomycin resistance (β-geo) cassette was used to identify heterozygous and homozygous animals. DNA (5 ng) was assayed using the Chromo4 real-time PCR system (MJ Research) and the Taqman Universal PCR Master Mix (Applied Biosystems) using manufacturer suggested protocols. Primers 5′-CCTGCTGATGAAGCAGAACA-3′ and 5′-TTGGCTTCATCCACCACATA-3′ and probe 5′-FAM CGCTGTTCGCATTATCCGAACCATTAMRA-3′ were used to amplify and detect β-geo. Primers 5′-TGCATAGCGTAATGTCCATGTTG-3′ and 5′-TCTCCTTCTGGGACATTGCTATC-3′ and probe 5′-VIC ACGGTTCTGCCTGTACGCCGATCA TAMRA-3′ were used to amplify and detect Ngf, which normalized for DNA concentrations. Eif2s2Trap offspring genotype was verified by PCR genotyping for the wild-type allele with primers F: 5′-AGGAACATAATTACAATGTGGCATAA-3′ (upstream of the gene-trap integration) and R: 5′-TCAAAGAAGGGGGAAATCCT-3′ (downstream of the gene-trap integration), and the Eif2s2Trap allele with primers F: 5′- TAAGGGTGTCGGATTTCCTG-3′ (upstream of the gene-trap integration) and R: 5′- GGCTACCGGCTAAAACTTGA-3′ (within the gene-trap). Chi-square goodness-of-fit tests were used to test for statistical differences between the observed and expected number of progeny.
This work was supported by National Institutes of Health grants CA75056 and CA119623.
We thank the CWRU Transgenic and Targeting Core for assistance with the generation of transgenic and gene-trap mice and the Department of Genetics Imaging Core for assistance with confocal microscopy.
Conflict of Interest statement. None declared.