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Oogenesis is the process by which ovarian germ cells undertake meiosis and differentiate to become eggs. In mice, Stra8 is required for the chromosomal events of meiosis to occur, but its role in differentiation remains unknown. Here we report Stra8-deficient ovarian germ cells that grow and differentiate into oocyte-like cells that synthesize zonae pellucidae, organize surrounding somatic cells into follicles, are ovulated in response to hormonal stimulation, undergo asymmetric cell division to produce a polar body, and cleave to form two-cell embryos upon fertilization. These events occur without premeiotic chromosomal replication, sister chromatid cohesion, synapsis, or recombination. Thus, oocyte growth and differentiation are genetically dissociable from the chromosomal events of meiosis. These findings open to study the independent contributions of meiosis and oocyte differentiation to the making of a functional egg.
Oogenesis is the process by which an ovarian germ cell becomes a female gamete, an egg. A functional egg is capable of undergoing fertilization and giving rise to a developing embryo, and it should contribute to that embryo exactly one copy of each chromosome. The former capability is achieved through growth and differentiation of the cell, while the latter is achieved through the chromosomal mechanics of meiosis. These cellular and chromosomal events of oogenesis are closely coordinated, but whether they are interdependent remains unknown.
In mice, early stages of germ cell development unfold identically in XX and XY embryos. In both sexes, primordial germ cells (PGCs) arise from the epiblast and migrate to the gonad1. There both XX and XY PGCs transition to become gametogenesis-competent cells (GCCs). Both XX and XY GCCs are competent to respond to signals from the gonadal soma to initiate meiosis and undergo sexual differentiation2,3.
The first morphological difference between germ cells in XX and XY gonads appears when meiotic chromosome condensation – a defining feature of prophase of meiosis I – occurs in ovarian (XX) germ cells during fetal development1,4. (Testicular germ cells do not enter meiotic prophase until well after birth). Thus, the fetal onset of meiotic prophase marks the onset of oogenesis. Indeed, fetal entry into meiotic prophase commonly serves as a proxy for subsequent oocyte growth and differentiation, and the absence of meiotic prophase is conventionally taken as evidence that fetal germ cells have adopted a spermatogenic fate1,4–10. This interpretation assumes that fetal meiotic initiation is necessary for oocyte growth and differentiation to occur –an assumption that has not been tested prior to the studies reported here.
Meiotic initiation is governed by the retinoic acid (RA)-responsive gene Stra811,12. Upon receiving the RA signal and expressing Stra8, ovarian germ cells replicate their chromosomes and enter prophase of meiosis I (hereafter “meiotic prophase”). Oocytes then progress through this prophase, arresting at its diplotene stage. A few days later, these cells differentiate to become primordial oocytes while remaining arrested in meiotic prophase. Throughout the reproductive life of the female, prophase-arrested primordial oocytes are recruited to differentiate into full-grown oocytes. (Meiosis is not resumed until ovulation and is not completed until fertilization.) Thus, in mice, oocytes grow and differentiate only after reaching the diplotene stage of prophase. Oocyte growth and differentiation during arrest in meiotic prophase are conserved in humans, frogs, flies, and worms, among other animals13,14. In rats the timing of primordial follicle formation can be altered by manipulating chromosome desynapsis (a hallmark of progression to diplotene and completion of prophase)15. Collectively, these observations are consistent with meiotic initiation and prophase being required for oocyte differentiation, which explains why many investigators have held this view.
Recent advances in embryonic stem (ES) and induced pluripotent stem (iPS) cell technologies have motivated efforts to derive oocytes in vitro from these and other undifferentiated cell types. Several laboratories have reported deriving cells that morphologically resemble oocytes16–22. Some reports of in vitro-derived oocyte-like cells did not directly assess the state of the chromosomes, drawing criticism from meiosis researchers23,24. In other cases the oocyte-like cells reportedly reduced their DNA content to 1C in vitro, in the absence of fertilization22; normally this would occur in female germ cells only upon fertilization. These difficulties in achieving proper coordination of oocyte differentiation and meiosis in vitro may reflect the underlying biology of oogenesis; they could be taken as evidence that differentiation and meiosis are regulated independently.
In this study we investigated the functional relationship between meiosis and oocyte differentiation in vivo. We found that Stra8-deficient germ cells, which do not initiate meiosis, can differentiate into oocyte-like cells. Morphological and functional analysis revealed that Stra8-deficient oocyte-like cells can synthesize zonae pellucidae, organize surrounding somatic cells into follicles, be ovulated in response to hormonal stimulation, undergo asymmetric cell division to produce a polar body, and cleave to form two-cell embryos upon fertilization. Direct analysis showed that these oocyte-like cells had developed without entering meiotic prophase or even undergoing premeiotic chromosome replication. We conclude that oocyte growth and differentiation can be genetically dissociated from premeiotic chromosome replication and the subsequent chromosomal events of meiosis. We postulate the existence of a Stra8-independent pathway, yet to be identified, that governs oocyte growth and differentiation.
Our prior studies of Stra8-deficient ovarian germ cells had been conducted in mice of mixed genetic background (not inbred)11. To ensure the reproducibility of our findings, we backcrossed the Stra8 mutant allele onto an inbred genetic background (C57BL/6) and characterized the meiotic defect in these mice (Supplementary Fig. 1). Corroborating our earlier findings11, C57BL/6 Stra8-deficient ovarian germ cells failed to properly assemble the synaptonemal complex, did not properly localize meiotic cohesin REC825, and did not form the DNA double-strand breaks (DSBs) essential for meiotic recombination26. This demonstrated that Stra8 is necessary for meiotic prophase in C57BL/6 females, which we employed in all subsequent experiments.
As we reported previously, fetal and postnatal loss of germ cells is accelerated in Stra8-deficient females; their ovaries had reduced numbers of germ cells at birth and were devoid of germ cells by six or eight weeks of age (Supplementary Fig. 2)11. Nonetheless, some Stra8-deficient germ cells evidently survived embryonic development despite the meiotic initiation block at E13.5 – E14.511. We confirmed this by comparing ovarian histology from wild-type and Stra8-deficient C57BL/6 animals between E14.5 and E16.5 (Supplementary Fig. 1d). To corroborate our prior conclusion11 that some Stra8-deficient germ cells survive postnatally, we stained postnatal day 2 (P2) ovarian sections for MVH (mouse vasa homolog; DDX4) protein, a marker of germ cells; we observed MVH-positive germ cells in both wild-type and Stra8-deficient ovaries (Supplementary Fig. 3). We then examined the oogenic potential of these surviving germ cells.
If entry into meiotic prophase is required for oocyte growth and differentiation, then the latter processes should not occur in Stra8-deficient ovarian germ cells. To test this, we compared ovarian histology of wild-type and Stra8-deficient females.
In a wild-type ovary, during the first postnatal week, a cohort of germ cells is recruited to grow and differentiate synchronously. Surprisingly, in Stra8-deficient ovaries, the surviving germ cells also began to grow and differentiate on a timetable similar to that of the first cohort in wild-type ovaries (Supplementary Fig. 4).
We next examined histological sections of Stra8-deficient ovaries at P21, when, in wild-type ovaries, growth and differentiation of the first cohort of oocytes are pronounced (Fig. 1a). In wild-type ovaries, we observed full-grown oocytes with large nuclei, called germinal vesicles (GVs). The perimeters of these large cells stained brightly using periodic acid-Schiff (PAS) reagent, indicating the presence of an oocyte-specific glycoprotein coat called the zona pellucida. Examining sections of ovaries from nine different Stra8-deficient animals, we found that all contained germ cells whose size and morphology were comparable to those of the wild-type oocytes. Like wild-type oocytes, these large Stra8-deficient germ cells featured GVs and zonae pellucidae, the latter of which we confirmed by staining sections for the zona pellucida protein ZP2 (Fig. 1b).
To examine the Stra8-deficient germ cells in greater detail, we generated electron micrographs of oocyte-like cells in large antral follicles of P21 Stra8-deficient females. This revealed ultrastructural characteristics indistinguishable from those of wild-type oocytes (Fig. 2)27. Cytoplasmic processes from cumulus cells traversed the zona pellucida, terminating at the surface of the Stra8-deficient oocyte-like cell. The cytoplasm of the oocyte-like cell contained structures typical of wild-type oocytes, including cortical granules, lattice structures, and oval vacuolated mitochondria (Fig. 2).
Despite the evidence that, as a population, germ cells in Stra8-deficient fetal ovaries fail to initiate meiosis and progress through meiotic prophase (Supplementary Fig. 1)11, the small number of germ cells surviving postnatally raised the possibility that these individual Stra8-deficient survivors had differentiated as oocytes after entering meiotic prophase. We excluded this possibility through a double-mutant (epistasis) experiment involving Stra8 and Dmc1. Dmc1-deficient ovarian germ cells die perinatally because Dmc1 is required for repair of DSBs that arise during meiotic prophase28–30. This death of Dmc1-deficient germ cells does not occur if DSB formation is prevented, for example in animals lacking a gene (Spo11) required for meiotic DSB formation31–33. We reasoned that if the surviving Stra8-deficient germ cells had entered meiotic prophase and formed meiotic DSBs, then no double-mutant (Stra8-deficient/Dmc1-deficient) germ cells should survive postnatally. However, if Stra8 deficiency stringently blocked meiotic initiation and DSB formation, then germ cell survival in the double mutant should resemble that in the Stra8 single mutant. We observed, as expected29,30,33, that Dmc1-deficient ovaries at P30 contained no germ cells (Fig. 3b). Double-mutant (Dmc1-deficient/Stra8-deficient) ovaries, however, contained oocyte-like cells similar to those of Stra8-deficient single-mutant ovaries (Fig. 3a, c). As the survival of Stra8-deficient oocyte-like cells does not require Dmc1, we conclude that these oocyte-like cells had not formed meiotic DSBs, reinforcing previous evidence that they had not entered meiotic prophase.
A critical function of wild-type oocytes is to actively organize somatic cells of the ovary into follicles, the hallmark of ovarian structure and function34. Like many wild-type oocytes, Stra8-deficient germ cells were enclosed in large follicles composed of multiple layers of cuboidal granulosa cells (Fig. 1), demonstrating their ability to drive folliculogenesis. By P30, large, preovulatory follicles were observed in 11 of 12 ovaries from six different Stra8-deficient animals (data not shown; Fig. 3a and and4c4c).
To extend this observation, we examined Stra8-deficient ovaries for expression of NOBOX, an oocyte-specific protein required for primary follicle formation35. We detected NOBOX protein in germ cells of all three Stra8-deficient and five control (wild-type or Stra8-heterozygous) ovaries examined by immunohistochemistry at P5 and P7 (Fig. 4a).
To confirm that proper granulosa cell differentiation had occurred in response to Stra8-deficient oocyte-like cells, we stained sections of wild-type and Stra8-deficient ovaries for FOXL2 protein, a key factor in granulosa cell differentiation and identity36,37. FOXL2 was expressed in the granulosa cells of both wild-type and Stra8-deficient ovaries at P10, when secondary follicles are present, and at P30, when large antral follicles are present. These findings confirm that Stra8-deficient oocyte-like cells support proper granulosa cell specification and differentiation (Fig. 4b, c).
We then asked whether oocyte-like cells in Stra8-deficient ovaries, together with surrounding somatic (cumulus) cells, could be ovulated. Because Stra8-deficient germ cells are lost before the animals reach sexual maturity, we could not assay natural ovulation. Instead, we hormonally stimulated wild-type and Stra8-deficient females at P20 to accelerate ovulation (“superovulation”) and flushed their oviducts to identify any ovulated cumulus-oocyte complexes (COCs). We isolated ovulated COCs from wild-type and from all five Stra8-deficient females subjected to this regimen. In wild-type females, cumulus cells of the preovulatory follicle secrete hyaluronic acid, causing expansion of the cumulus cell mass (the “cumulus oophorous”) that surrounds the oocyte. This process depends on the oocyte, and competence to support cumulus oophorous expansion is acquired late in oogenesis38. Examination of wild-type and Stra8-deficient ovulated COCs revealed that cumuli oophori were fully expanded in both groups (Fig. 4d). We conclude that Stra8-deficient oocyte-like cells can be ovulated with expanded cumuli oophori, implying that they can interact with the ovarian soma in a way that resembles wild-type oocytes.
In wild-type females, full-grown GV-stage oocytes are arrested in diplotene of the first meiotic prophase. At ovulation, wild-type GV-stage oocytes resume meiosis, breaking down the nuclear envelope, condensing their chromosomes, and dividing asymmetrically to form a large secondary oocyte and a smaller polar body. Competence to undergo this division is acquired in late stages of oocyte growth and differentiation, making it a defining functional feature of a full-grown oocyte39. Two mutants that are defective in individual aspects of meiotic prophase (synapsis or recombination) have been reported to produce polar bodies40,41, but it is not known whether blocking meiotic initiation (preventing the chromosomal program in its entirety) would preclude this asymmetric division. We therefore asked whether Stra8-deficient oocyte-like cells could produce polar bodies.
Full-grown wild-type oocytes can be induced to undergo maturation by removing them from follicles42. We extracted cumulus-oocyte complexes from P22 wild-type and Stra8-deficient ovaries by follicle puncture and cultured them overnight. We then mechanically removed the cumulus cells and visually assayed polar body formation. Most Stra8-deficient cells underwent germinal vesicle breakdown (GVB) – the first step on the path to polar body formation. Of the cells that underwent GVB, 28 of 35 wild-type oocytes and 11 of 42 Stra8-deficient oocyte-like cells formed polar bodies (Fig. 5), demonstrating that Stra8-deficient cells can undergo maturation and an asymmetric division. (We also observed polar body formation in vivo, following superovulation [Supplementary Fig. 5], corroborating our findings in vitro.)
The failure of many Stra8-deficient oocyte-like cells to produce polar bodies was likely due to a failure of spindle assembly in the absence of paired homologous chromosomes. Of 31 Stra8-deficient cells that underwent GVB but did not produce polar bodies, seven cells fragmented, while the other 24 cells remained arrested without a visible GV or polar body. The latter group of cells contained aberrant spindles reminiscent of those observed in Mlh1-deficient oocytes, which fail to maintain homologous chromosome pairing (Supplementary Fig. 6)40.
We reported previously that fetal germ cells in Stra8-deficient females fail to undergo premeiotic chromosome replication11. Accordingly, we tested whether the Stra8-deficient oocyte-like cells had replicated their chromosomes. First we compared DAPI intensity in GV-stage wild-type oocytes and Stra8-deficient oocyte-like cells. Using this crude approach, we found that wild-type oocytes, with replicated chromosomes, contained significantly more DNA than Stra8-deficient oocyte-like cells (Supplementary Fig. 7).
To validate this preliminary observation, we examined the configuration of chromosomes in Stra8-deficient oocyte-like cells that had matured to produce polar bodies. Haploid mouse gametes have 20 chromosomes, and diploid cells have 40 chromosomes. In wild-type females, postnatal GV-stage oocytes have 40 cohesed pairs of sister chromatids – 80 chromatids in all – as a consequence of premeiotic chromosome replication having occurred during fetal development. (The number of chromatids is subsequently halved, during the first meiotic division, and halved again during the second meiotic division.)
Following the first division, chromatids (more precisely, their centromeres – one per chromatid) can be visualized and counted in the oocyte and polar body. We stained in vitro-matured cells with DAPI, anti-tubulin antibody, and anti-centromere antibody (ACA) to visualize, respectively, DNA, the spindle, and centromeres. We mounted stained cells on slides in a manner that preserved three-dimensional structure, and we collected Z-stacks of images through the entire volume. We then counted centromeres and visualized the configurations of sister chromatids in both the oocyte (or oocyte-like cell) and its adjoining polar body.
As expected, in each of 16 wild-type samples, we observed a total of 80 chromatids: 20 pairs of cohesed chromatids in the matured oocyte and another 20 pairs of cohesed chromatids in the polar body (Fig. 6a, b). By contrast, in each of 11 Stra8-deficient samples, we observed a total of 40 uncohesed chromatids distributed unevenly between the oocyte-like cell and the polar body (Fig. 6a, b). Examination at high magnification confirmed that while wild-type oocytes contained cohesed sister chromatids, Stra8-deficient oocyte-like cells contained single chromatids (Fig. 6a, b insets). The only explanation for this chromosomal configuration is that, prior to maturation and polar body formation, these Stra8-deficient oocyte-like cells had 40 uncohesed chromatids – as would be found in a premeiotic germ cell that had not replicated its chromosomes. In the absence of pre-meiotic replication and meiotic prophase, bi-polar spindle attachment of homologous chromosomes would not have been possible. This evidently led to chaotic chromosome segregation, with one, both, or neither member of each homologous chromosome pair being apportioned to the polar body (Fig. 6c).
Taken together, these results argue strongly that Stra8-deficient germ cells completed oocyte-like differentiation and maturation without having undergone premeiotic chromosome replication and without having entered meiotic prophase.
Since Stra8-deficient oocyte-like cells have only 40 chromatids (as opposed to 80 in wild-type oocytes), which they segregate in an apparently haphazard manner, the probability of achieving a euploid egg that could yield a live-born pup is remote. Nevertheless, we wondered whether these oocyte-like cells could undergo fertilization and support early events of embryogenesis. To address this question we performed in vitro fertilization (IVF) experiments using control (wild-type or Stra8-heterozygous) oocytes and Stra8-deficient oocyte-like cells harvested by superovulation of juvenile females as described earlier (Fig. 7). Six hours after IVF, we observed that control oocytes and Stra8-deficient oocyte-like cells had extruded a second polar body and contained two pronuclei, indicating successful fertilization. At 22 hours, 52 of 68 control oocytes and 7 of 39 Stra8-deficent oocyte-like cells had progressed to become two-cell embryos. At 48 hours, control two-cell embryos had progressed to the four-cell stage, but all Stra8-deficent embryos remained arrested at the two-cell stage. These results demonstrate that meiotic initiation and prophase are not required for formation of fertilization-competent egg-like cells, or for the subsequent division that gives rise to two-cell embryos.
We investigated the functional relationship between two components of oogenesis: meiosis, and cellular growth and differentiation. Using in vivo genetic analysis, we demonstrated that growth and differentiation are dissociable from the chromosomal events of meiosis. Although meiosis is an essential part of oogenesis and absolutely required for orderly chromosomal segregation, we found that fertilization-competent oocyte-like cells can develop in its absence (Fig. 8).
We previously reported that Stra8-deficient ovarian germ cells fail to initiate meiosis during fetal development11. Here we confirmed our previous findings on an inbred genetic background. We extended these observations by directly examining the chromosomes of postnatal Stra8-deficient germ cells during the first wave of oogenesis. We found that the chromosomal content and configuration of Stra8-deficient germ cells remained identical to that of premeiotic germ cells that had not replicated their chromosomes – even many weeks after wild-type germ cells would have initiated meiosis. This finding highlights a fundamental difference between the Stra8-deficient phenotype and the meiotic phenotypes of mice deficient for Spo11, Dmc1, Rec8, Sycp1, Sycp3 or Mlh1, among others. These meiotic mutants enter prophase of meiosis I, and their defects are limited to a subset of meiotic chromosomal processes29,30,32,41,43–45. In contrast, the Stra8 mutant does not undergo any of the chromosomal events associated with prophase of meiosis I and therefore is non-meiotic. The Stra8 mutant represents a unique and powerful tool with which to study ovarian germ cell differentiation in the absence of meiosis.
Following our original report that Stra8 is required for meiotic initiation in the fetal ovary, other investigators inferred – given prevailing models – that Stra8 must also be required for oocyte differentiation7,9,10,46,47. To the contrary, we report that Stra8 function, and hence meiotic initiation and prophase, are not required for oocyte differentiation as judged by morphological criteria, molecular markers, and functional assays. In the absence of meiosis, Stra8-deficient ovarian germ cells can develop a large cytoplasm, synthesize zonae pellucidae, organize surrounding somatic cells into follicles, acquire competence for fertilization and the first cleavage division, undergo asymmetric cell divisions to form polar bodies, and be ovulated in response to hormonal stimulation. We conclude that oogenesis in mice is a genetically dissociable union of two concurrent processes – meiosis and differentiation – and that meiotic initiation and prophase are not prerequisite to oocyte differentiation (Fig. 8). We postulate the existence of a Stra8-independent pathway, yet to be identified, that regulates oocyte growth and differentiation (Fig. 8). More broadly, our findings open to study the independent contributions of meiosis and oocyte differentiation to the making of a functional egg.
Our findings should also motivate a reevaluation of hypotheses concerning mouse germ cell sex determination, that is, how a primordial germ cell chooses between becoming an egg or a sperm. For decades, experimentalists have interpreted the presence or absence of fetal meiotic prophase as a proxy for commitment to, respectively, oogenesis or spermatogenesis1,4–10. In contrast, our finding of oocyte-like growth and development in Stra8-deficient germ cells clearly demonstrates that the absence of meiotic prophase is not, by itself, evidence that fetal germ cells have adopted a spermatogenic fate. Conversely, entry into meiotic prophase should no longer be taken, by itself, as evidence that experimentally manipulated fetal germ cells have adopted an oogenic fate. For these reasons, many published conclusions regarding the timing and control of mouse germ cell sex determination must be reconsidered, and new phenotypic endpoints and assays adopted.
Our work also suggests additional opportunities for future study. Since the occurrence of oocyte growth and differentiation during meiotic prophase arrest is broadly conserved13,14, we wonder whether oocyte differentiation is genetically dissociable from meiosis in other vertebrate or invertebrate animals. A gene orthologous to mouse Stra8 has been identified in the Xenopus genome (XM_002941430), but its roles, if any, in meiotic initiation and oogenesis remain unknown. It should also be possible to address this question in other animals once genes required for meiotic initiation are identified.
Indeed, it has been reported that sporulation is dissociable from meiosis in yeast, and that gametogenesis is dissociable from the meiotic pattern of chromosome segregation in Arabidopsis48,49. Most recently the sperm-oocyte decision has been decoupled from the mitosis-meiosis decision in C. elegans50. Going forward, it will be of great interest to explore similarities and differences among these diverse eukaryotic systems with respect to the separability of meiosis and gamete differentiation.
In Stra8-deficient ovarian germ cells, how does the non-meiotic 2C diploid genome drive oogenic growth and differentiation in a manner that so closely resembles that of the meiotic-prophase-arrested 4C diploid genome of a wild-type oocyte? This might be addressed in the future by assessing the epigenetic and transcriptional status of the Stra8-deficient oocyte-like cells – recognizing that it will be challenging to obtain those cells in substantial numbers.
Following in vitro fertilization of Stra8-deficient egg-like cells, we observed seven embryos that progressed to but not beyond the two-cell stage. A full understanding of this arrest at the two-cell stage – a time when activation of the zygotic genome occurs in wild-type embryos51 – will require further investigation. The arrest may be due to activation of a grossly aberrant zygotic genome, with the non-meiotic Stra8-deficient egg-like cells having contributed chaotic samplings of chromosomes to their respective embryos. Indeed, one would expect these embryos to be monosomic for several autosomes (or in some cases trisomic) and about one quarter to have no X chromosome. The question arises whether the cytoplasm of a non-meiotic, Stra8-deficient oocyte-like cell would be capable of supporting embryogenesis beyond the two-cell stage if presented with a normal complement of chromosomes. This might be tested by nuclear transplantation, with the results illuminating the limits of oogenic differentiation in the absence of meiosis.
As described here and in our previous report11, the absence of Stra8 function accelerates the germ cell loss that is a prominent feature of the wild-type ovary; here, as in the wild-type ovary, we do not know the cause(s) of this germ-cell death. It is probably not due to checkpoints usually associated with progression through meiotic prophase since DSBs and asynapsed axial elements, recognized by DNA damage or asynapsis checkpoints respectively, are absent in the Stra8-deficient oocyte-like cells33,52.
Our findings may have practical implications, for infertility and for in vitro oogenesis. Oocyte-like differentiation without meiosis may explain some cases of infertility, especially where women cannot achieve or sustain pregnancy despite the presence of cells that histologically resemble oocytes. Similarly, some recent reports of mouse or human oocytes derived from cells grown in culture16–22 may actually be demonstrating oocyte-like differentiation without meiosis23. Our observations illustrate that claims of successful oogenesis in vitro cannot rest solely on evidence of oocyte-like differentiation, because oocyte-like morphology and functionality can arise in the absence of meiotic initiation and meiotic prophase. Therefore, meiotic initiation and progression must be documented directly. Recently, successful oogenesis from ES and iPS cells was achieved in mice by culturing induced PGC-like cells within gonadal aggregates followed by transplantation to the ovary of an adult female53. Understanding the functional interdependencies, if any, of meiosis and oocyte differentiation may help to move this technology entirely in vitro.
Stra8-deficient mice were generated and backcrossed as previously described11,12. All Stra8 animals used were backcrossed to C57BL/6NtacfBR for at least 18 generations. Dmc1-deficient mice 28, which had been backcrossed to C57BL/6J for at least 10 generations, were purchased from Jackson Laboratory. Stra8-deficient females were generated by mating heterozygotes. Dmc1-deficient females and Stra8/Dmc1 double-deficient females were generated by mating Stra8 Dmc1 double heterozygotes. All experiments involving mice were approved by the Committee on Animal Care at the Massachusetts Institute of Technology.
Dissected ovaries were fixed in Bouin’s solution (Polysciences) overnight at 4°C, embedded in paraffin and sectioned. Slides were stained with periodic acid-Schiff (PAS) reagent (Sigma) according to the manufacturer’s protocol and counter-stained with Mayer’s modified hematoxylin (Invitrogen). For every genotype at least four samples were analyzed.
Ovaries of 21-day-old mice were fixed in 85% Karnovsky’s fixative and trimmed in the fixative to individual antral follicles. Samples were prepared for electron microscopy using standard procedures.
Ovarian germ cell spreads were prepared according to a published protocol54. Cells were permeabilized with 0.5% Triton-X100 for 5 minutes and blocked with 1% BSA for 1 hour. Rabbit anti-SYCP3 (Abcam) was used at a 1:1000 dilution. Rabbit anti-REC8 (courtesy of C. Heyting, Agricultural University, Wageningen, Netherlands) was used at a 1:250 dilution.
Dissected ovaries were fixed in Bouin’s solution or 4% paraformaldehyde overnight at 4°C, embedded in paraffin and sectioned. Slides were de-waxed in xylenes, re-hydrated through an ethanol gradient and boiled in sodium citrate buffer (pH 6.0) for 15 minutes. For colorimetric immunohistochemistry, slides were pre-treated for 10 minutes with 0.3% H2O2. Mouse monoclonal anti-γH2A.X (Millipore) was used at a 1:100 dilution. Goat anti-hVASA (R&D Systems) was used at a 1:250 dilution. Rat monoclonal anti-ZP2 (Santa Cruz) was used at 1:100 dilution. Rabbit anti-NOBOX (Abcam) was used at a 1:1000 dilution. Goat anti-FOXL2 (Abcam) was used at 1:500 dilution.
Female mice were stimulated with 5 international units (IU) of pregnant mare serum gonadotropin (PMSG) (Sigma) at postnatal day 20 (P20). Forty-four to 48 hours after PMSG injection, the animals were stimulated with 5 IU of human chorionic gonadotropin (hCG) (Sigma). Fifteen to 16 hours after the second injection, the animals were sacrificed and their oviducts were dissected away from the uterus and ovaries. Oocytes were released by slicing open the oviducts and allowing the COCs to spill into a drop of KSOM (potassium simplex optimized medium) (Millipore) under oil. Cumulus cells were removed by treating COCs with hyaluronidase (Sigma) for 5 minutes and washing twice in KSOM.
Female mice were stimulated with 5 IU of PMSG at P20. Forty-four to 48 hours after injection, animals were sacrificed and ovaries dissected. COCs were isolated by follicle puncture and cultured overnight in MEM-α supplemented with 0.3% BSA. The next day, cumulus cells were removed mechanically, and polar body formation was assessed.
GV-stage oocytes were isolated by follicle puncture, mechanically denuded and spread by drying down on slides wetted with 1% parafarmaldehyde. Slides were imaged using constant exposure time across all samples. DAPI intensity was quantified using CellProfiler software.
In vitro-matured oocytes were fixed in 4% parafarmaldehyde for 45 minutes, permeabilized with 0.1% Triton-X100 and blocked with 10% donkey serum. Monoclonal rat anti-tubulin [YL/2] (Abcam) was used at a 1:250 dilution. Human anti-centromere antibody (ACA) (Antibodies, Inc.) was used at a 1:100 dilution.
Images were acquired using a DeltaVision deconvolution microscope (AppliedPrecision). For oocytes and oocyte-like cells, Z-stacks were collected at 0.5 μm spacing. All images within the stacks were deconvolved using DeltaVision softWoRx software. Z-stack projections were generated using the maximum intensity method in ImageJ. ACA signals were counted on projected images. Individual images from the Z-stacks were used to resolve centromeres that were superimposed in the Z plane.
Superovulated COCs were collected as described earlier and maintained in MEM-α (minimum essential medium alpha) (Invitrogen) supplemented with 5% fetal bovine serum (FBS) to prevent zona pellucida hardening. To collect sperm, epididymi were dissected from adult males and cut to release sperm in serum-free MEM-α supplemented with 0.3% bovine serum albumin (BSA) (Sigma). COCs were washed out of serum into MEM-α supplemented with 0.3% BSA and added to sperm, which had been diluted 1:90 in MEM-α supplemented with 0.3% BSA under oil. Fertilization dishes were incubated for 6 hours before washing away sperm and then incubated overnight. Two-cell embryos were transferred to KSOM for further culture.
We thank C. Heyting for REC8 antiserum, Nicki Watson and Lesley Bechtold for assistance with electron microscopy, and A. Amon, D. Bellott, M. Carmell, I. Cheeseman, D. de Rooij, R. Desgraz, T. Endo, G. Fink, A. Hochwagen, Y. Hu, J. Hughes, B. Lesch, J. Mueller, L. Okumura, T. Orr-Weaver, K. Romer, and S. Soh for advice and comments on the manuscript. Supported by the Howard Hughes Medical Institute and the National Institutes of Health (HD23839).
AUTHOR CONTRIBUTIONSG.A.D., A.E.B., J.J.E., and D.C.P. designed the experiments. G.A.D. and J.J.E. performed the experiments. G.A.D and D.C.P. wrote the manuscript.
CONFLICT OF INTEREST
The authors have no competing financial interests.