Germline Progenitors Escape the Widespread Phenomenon of Homolog Pairing during Development

Summary

Homolog pairing, which plays a critical role in meiosis, poses a potential risk if it occurs in inappropriate tissues or between nonallelic sites, as it can lead to changes in gene expression, chromosome entanglements, and loss-of-heterozygosity due to mitotic recombination. This is particularly true in Drosophila, which supports organismal-wide pairing throughout development. Discovered over a century ago, such extensive pairing has led to the perception that germline pairing in the adult gonad is an extension of the pairing established during embryogenesis and, therefore, differs from the mechanism utilized in most species to initiate pairing specifically in the germline. Here, we show that, contrary to long-standing assumptions, Drosophila meiotic pairing in the gonad is not an extension of pairing established during embryogenesis. Instead, we find that homologous chromosomes are unpaired in primordial germ cells from the moment the germline can be distinguished from the soma in the embryo and remain unpaired even in the germline stem cells of the adult gonad. We further establish that pairing originates immediately after the stem cell stage. This pairing occurs well before the initiation of meiosis and, strikingly, continues through the several mitotic divisions preceding meiosis. These discoveries indicate that the spatial organization of the Drosophila genome differs between the germline and the soma from the earliest moments of development and thus argue that homolog pairing in the germline is an active process as versus a passive continuation of pairing established during embryogenesis.

Introduction

During meiosis, the germline nucleus undergoes extensive reorganization to accurately align homologous chromosomes along their entire length, enabling them to recombine and ultimately segregate from one another. Outside of the germline, however, homolog pairing, if it occurs at all, is usually transient and localized to a particular chromosomal region [1]–[7]. Indeed, the individual somatic chromosomes of many eukaryotes occupy distinct territories in the nucleus [8]–[10], which would be expected to minimize interactions between homologous chromosomes and thus pairing-mediated changes in gene expression, chromosome entanglements, and loss-of-heterozygosity due to mitotic recombination [11]–[17]. Consequently, extensive homolog pairing is generally considered a germline-specific phenomenon that is restricted to the early stages of meiosis.

One striking exception is found in Dipteran insects, such as Drosophila, where there is widespread homolog pairing in somatic cells. Such pairing has been documented in embryonic, larval, and adult tissues, with pairing frequencies at individual loci reaching 80% or more [18]–[23]. These observations have led researchers to speculate that Drosophila represents a major departure from other organisms in terms of nuclear organization. The implications are especially profound with respect to the germline, where it has been widely presumed that the homolog pairing observed during Drosophila meiosis is an extension of the pairing established during embryogenesis [24]–[30]. Notably, there is evidence for homolog pairing being in place during the mitotic divisions immediately preceding meiosis, consistent with it having been established much earlier in development [27], [29], [31]. Indeed, such pre-meiotic pairing has been reported to continue uninterrupted into meiosis [27], [29], [31], which may explain the ability of Drosophila females to maintain interactions associated with meiotic pairing and form the synaptonemal complex (SC) between homologs in the absence of double-strand breaks (DSBs) [32], induction of which is essential for pairing and SC formation in yeast and mammals.

This early pairing in the Drosophila germline is in stark contrast to meiotic pairing in nonDipteran organisms consisting of distinct soma and germline tissues [30], [33]–[35]; while a recent study showed pairing as early as the final round of pre-meiotic replication in mice, there was no demonstration of pairing earlier to this time point [36]. Here we clarify the origin of germline pairing in Drosophila, refuting a long-held hypothesis that it derives from pairing established during embryogenesis and arguing, instead, for a program of germline pairing that is not initiated until the five mitotic cell cycles just prior to meiosis.

Results and Discussion

Homologous chromosomes enter the germline unpaired

To determine whether chromosomes are paired prior to meiosis in Drosophila, we first analyzed adult germline stem cells (GSCs), focusing on the female germline, as meiosis in male Drosophila does not follow “the standard meiotic script” [26], [37]. The GSC of the Drosophila female are found in its two ovaries, the very tip of which consists of ∼16–20 germaria, each of which harbors just one or two GSCs positioned adjacent to the somatic niche [38]. During oogenesis, each GSC divides asymmetrically to produce a renewed stem cell and a differentiating cystoblast (CB), which is positioned distal from the niche and destined to undergo four more rounds of replication and division before entering meiotic prophase (Figure 1A). In order to identify the GSCs and distinguish them from subsequent pre-meiotic stages, we took advantage of an antibody to the cytoplasmic protein SXL, levels of which increase in GSCs and then decrease as differentiation proceeds [39].

Chromosome positioning in individual GSC nuclei was assessed by fluorescent in situ hybridization (FISH) in whole-mounted tissues, using techniques that preserve the nuclear architecture followed by high-resolution microscopy and 3D-image reconstruction. Within each nucleus, a single FISH signal or two signals separated by ≤0.8 µm were considered to represent the paired state of the targeted locus. To evaluate the extent of genome-wide pairing, we used nine FISH probes (Figure 1B and Table S1). Three probes targeted highly repeated sequences of the centromeric heterochromatin, including that of the X chromosome (359), chromosome 2 (AACAC), and chromosome 3 (dodeca). The remaining six probes were generated with Oligopaint technology [40] and targeted single copy euchromatic loci, including two loci (5A and 16E) on the X chromosome, loci on the left (24D) and right (50D) arms of chromosome 2 and the left (69C) and right (100B) arms of chromosome 3. Importantly, these probes were extremely efficient, with 100% of nuclei displaying at least one focus for each probe.

In stark contrast to the assumption that meiotic pairing is an extension of pre-existing somatic pairing and that chromosomes therefore enter the germline in the paired state, we observed extensive separation of homologs in GSCs. Eight out of the nine loci produced two distinct FISH signals in the majority of, if not all, nuclei and were considered unpaired in 75–100% of GSC nuclei (Figure 1C–D) in experiments representing 15–30 ovaries. In fact, the average inter-allelic distances for these loci was equivalent to the radius of the nucleus (2.29 µm; p>0.05, unpaired t test; Table S1), consistent with a random positioning of the maternal and paternal chromosomes relative to each other. The dramatic deficiency of pairing at these eight loci argues that the genome-wide homolog pairing and subsequent SC formation during meiosis does not derive from a paired state that is extant in the GSC.

The one exception was the X-linked 359 repeat, which was paired in 80% of GSC nuclei (Figure 1D). While this may be indicative of some homolog alignment in GSCs, it may also reflect the proximity of this locus to the rDNA gene cluster, which is spatially confined to the nucleolus, and/or the large size of this repeated region [20], [28], [41], estimated to be 11 Mb in size [42]. Importantly, two other euchromatic loci proximal (16E) and distal (5A) to the 359 repeat were mostly (75%) and completely (100%), respectively, unpaired, indicating that the X-chromosome is not exceptional in its capacity to pair in GSCs. We have also found the 359 repeat to exhibit atypical pairing dynamics in somatic cells [43].

Homolog pairing is established during the mitotic cell cycles prior to meiosis

The largely unpaired state of GSCs shifted our focus to determining whether, outside of the 359 repeat, pre-meiotic pairing occurs in the female germline to any significant extent. To this end, we looked directly downstream of the GSCs to the differentiating CBs, which number between one and two per germarium and, relative to the GSCs, are positioned downstream of the niche. Here, we targeted the euchromatic loci of 5A, 16E, 24D, 50D, 69C, and 100B (Figure 1D and Table S1) and found unambiguous levels (11–35%) of pairing at all but 5A. These findings establish that Drosophila does, indeed, support at least some degree of pairing well before meiosis initiates.

Despite significant levels of euchromatic pairing in CBs, no pairing was detected at the centromeric repeats AACAC and dodeca, suggesting the partial nature of homolog pairing at this stage. In fact, when we performed two-color FISH targeting two loci across a single arm of chromosome 2 in CB nuclei, we did not detect any pairing of the centromeric locus despite 33% (n = 21) pairing of the chromosome arm (Figure 1E).

The partial pairing observed in CBs raised the possibility that complete pairing can be achieved in cells progressing through mitotic divisions prior to the initiation of meiosis. In Drosophila, this program includes four rounds of divisions in which the CB becomes a 2-, 4-, 8-, and ultimately 16-cell cyst of interconnected cystocytes, one of which completes meiosis. Importantly, these stages precede the pachytene stage of meiosis, in which homologous chromosomes are fully synapsed (Figure 2A). In order to evaluate the progression of pre-meiotic pairing, we used the P[bamP-GFP] transgene, a transcriptional reporter that is not expressed in GSCs or pachytene, but is expressed in each of the intervening pre-meiotic stages [39], [44], along with an antibody against Spectrin, a cytoskeletal protein that forms a spherical structure called the spectrosome in GSCs and CBs, and an antibody against C(3)G, which identifies the SC in meiotic nuclei [45] (Figure 2A–C). Developing cysts were staged based on the number of BAM-positive cells and by Spectrin staining, which, in cysts, localizes to a branched structure called the fusome. We found that homolog pairing levels rapidly increased through the divisions, with each of six FISH targets reaching maximum levels of pairing (87–95%) by the 8-cell cyst (Figure 2D). Once maximum levels of pairing were achieved, they were maintained throughout the remaining pre-meiotic divisions and into the pachytene stage of meiosis (Figure 2C–D), suggesting that homologous chromosomes initiate pairing up to four mitotic divisions prior to meiosis and enter meiosis fully aligned. Importantly, we were able to assess pairing in all four cells of twenty-seven 4-cell cysts, where 87%, 90%, 100%, and 95% of cells showed pairing at dodeca, 24D, 69C, and 100B, respectively. Because the oocyte derives from one cell of a 4-cell cyst, these observations demonstrate that pairing can be observed well before the initiation of meiosis. Analogous data were obtained for the 8-cell and 16-cell cysts.

Interestingly, not all chromosome loci achieved pre-meiotic pairing at the same rate; the 359, 24D, and 100B loci reached maximum levels of pairing prior to the 5A, AACAC, dodeca, and 69C loci by one to four divisions (Figure 1D and Figure 2D). This observation is consistent with the higher level of euchromatic as versus centromeric pairing we observed for autosomes in CBs and suggests that, rather than strictly initiating at the centromeres, where SC formation is first observed [46], [47], germline pairing may initiate at different rates or times across the genome.

Chromosomes maintain an unpaired state throughout germline development

The results described above refute the long held belief that homolog pairing in Drosophila meiosis is an extension of pairing events established within the embryo and maintained throughout development in all tissues, including the germline. Hence, they encouraged us to assess whether germline cells ever support somatic levels of homolog pairing during development or, alternatively, whether unpairing represents a global nuclear reorganization specifically in the GSCs. We, therefore, evaluated pairing levels during embryogenesis, as this 24-hour phase of development marks both the onset of somatic homolog pairing as well as the separation of germline and somatic lineages. The germline distinguishes itself ∼2 hours after egg lay (AEL), with the primordial germ cells (PGCs), from which adult GSCs are derived, forming at the posterior pole of the embryo and becoming identifiable with the germline-specific protein marker VASA [48] (Figure 3A–B). Examination of homologous pairing during embryogenesis has indicated that some sites attain pairing as early as 2 hours AEL [21]. In fact, the ∼500 Kb histone locus on chromosome 2 has been reported to pair ∼2.5 hours AEL in the soma and PGCs [21], providing reason to believe that PGCs do not differ from somatic cells in their capacity to pair. However, it is unclear if pairing of this locus reflects genome-wide levels or specific features of this locus, such as its transcriptional activity [17], [20], [21], [28], [49], [50]. Here, we distinguish these alternatives by examining the behavior of four other loci across the genome - two centromeric (AACAC and dodeca) and two single-copy euchromatic loci (24D and 50D).

Confirming our ability to detect the onset of pairing in somatic cells, we examined embryos 2.5 hours AEL and observed, respectively, 12% and 10% pairing at the centromeric AACAC and dodeca repeats and 22% and 29% pairing at the euchromatic 24D and 50D loci (Figure 3C). In contrast, the PGCs at the posterior pole of the embryos consistently exhibited lower levels of pairing at this stage for all four loci, ranging from 3% to 5% (Figure 3C). We next analyzed embryonic nuclei 14 hours AEL and found 80–100% of somatic nuclei were paired for each of the four loci (Figure 3D), levels consistent with full attainment of somatic homolog pairing [21]. Strikingly, however, homologous chromosomes in the PGCs, which at 14 hours AEL are in contact with somatic cells, remained essentially unpaired, attaining only 0–7% pairing at any of the four loci (p<0.0001; Figure 3D). In these cells, the inter-allelic distances were extensive, averaging 2.5–3.5 µm and, in some cases, reaching as much as 5–6 µm (Figure S1). Additionally, sex-specific differences were not observed, suggesting that, regardless of sex, germline progenitors do not support genome-wide homolog pairing (Figure S2). Thus, PGCs maintain a predominantly unpaired state of homologous chromosomes throughout embryogenesis. These observations argue that germ cells are never exposed to the widespread pairing observed in somatic cells and thus, represent the only Drosophila tissue identified so far that escapes this phenomenon.

Germline progenitors have large nuclear volumes with chromosomes juxtaposed to the nuclear envelope

To better understand how germline progenitors maintain an unpaired state, we determined whether they might exhibit other distinctive features of nuclear organization. Notably, we observed that the nuclear volumes of PGCs 14 hours AEL (172.5 µm³) were ∼3.3 fold greater than that of neighboring somatic cells (52.3 µm³, p<0.0001; Figure 4A) and reasoned that larger nuclear volumes could cause increased distances between homologs and thus account for the lower levels of pairing in PGCs. Consistent with this hypothesis, the nuclear volumes of GSCs and CBs (50.5–52.7 µm³) were greater than two times larger than that of the surrounding somatic follicle cells (21.3 µm³, p = 0.0027; Figure 4B), while those of the 8-cell cysts and cells in pachytene were approximately the same or smaller in size (Figure 4B). To test the potential of larger nuclear volumes to explain lower levels of pairing, we normalized inter-allelic distances to the nuclear radius. This analysis revealed that, even when inter-allelic distances were normalized, the level of pairing in PGCs remained less than that observed in somatic cells by six to nineteen fold (Figure S3). This outcome suggests that the separation of homologous chromosomes cannot be fully explained by nuclear volume alone.

We next analyzed the global distribution of DNA within the larger GSC nuclei and found a distinct nuclear 4′,6-diamidino-2-phenylindole (DAPI) staining pattern compared to somatic follicle cells, indicating a change in chromatin structure. As shown in Figure 4C, surface plots of DAPI fluorescence intensity revealed a non-uniform peripheral staining pattern in GSC nuclei. In contrast, the DAPI fluorescence intensity in adjacent somatic follicle cell nuclei typically displayed a relatively uniform and diffuse staining pattern (Figure 4C). To assess whether this DNA distribution could result from the juxtaposition of chromosomes to the nuclear envelope, we used FISH in combination with an antibody against lamin to measure the distance between the nuclear envelope and each of three loci across chromosome 2: the AACAC centromeric repeat and the 24D and 50D loci in the middle of each arm. As predicted, all three loci were equally close to the nuclear envelope in GSCs, with average distances of only 15–20% of the total nuclear radius (Figure 4D). Similar results were found for the nuclei of CB, 8-cell cysts, pachytene cells, as well as embryonic PGCs (Figure 4D and Figure S4), indicating that the peripheral localization of chromosomes is adopted early in germline development and maintained into meiosis. In contrast, the same three loci in somatic cells exhibited greater distances from the nuclear envelope, averaging of 25–47% of the radius, with the centromeric locus closest to the nuclear envelope (Figure 4D and Figure S4). This arrangement, in which centromeres are located in the periphery with chromosome arms displaced across the nuclear space, is consistent with the Rabl configuration of chromosomes frequently found in Drosophila somatic cells [51], [52]. We conclude that germline cells may adopt a distinct nuclear structure which, compared to somatic cells, involves placement of chromosomes in close proximity to the nuclear envelope along their entire length.

Conclusion

Our findings reveal extensive separation of homologous chromosomes in germline progenitors from early embryogenesis until the five mitotic cell cycles just prior to meiosis and, in this regard, align Drosophila with other organisms that establish homolog pairing de novo in the gonad. Importantly, our observations are in agreement with Christophorou et al. (also in this issue), who also found a deficiency of homolog pairing in the GSCs of the Drosophila adult female. The lack of pairing in germline progenitors is especially noteworthy, considering the widespread prevalence of pairing in the somatic tissues of Drosophila. Why should an organism ensure homologous chromosomes remain unpaired in germline progenitors, only to allow pairing beyond the stem cell divisions? One possibility is that, since germline progenitors generate the entire cell population responsible for transmitting the genome to subsequent generations, any negative outcome of that pairing could be propagated to a much greater extent as compared to undesired events occurring downstream of the GSCs and thus have a higher probability of multigenerational consequences.

Our discovery of unpaired homologs in germline progenitors also demonstrates that homolog pairing is not an inevitable feature of Drosophila chromosomes and is consistent with studies arguing that pairing is a controlled process reflecting genes that promote pairing as well as those that antagonize it [14], [15], [22], [23], [43], [53]. Here, we further propose that potentially undesirable homologous interactions are precluded in Drosophila germline progenitors coordinately with, or due to, the separation of the progenitors from the soma in early embryogenesis. Pairing could also be precluded through a localization of chromosomes to the nuclear periphery. Such a configuration could lead to the formation of chromosome territories that separate homologs in the germline, as opposed to configurations that permit or even promote the pairing observed in the soma (Figure 5). Note that our data do not clarify whether the mechanisms that pair homologous chromosomes in somatic cells are distinct from, or similar to, those that eventually pair homologous chromosomes in the pre-meiotic cells. Nevertheless, to the extent that the mechanisms may be different, our findings are consistent with the notion that germline nuclei may suppress or delay the mechanisms that support pairing in the soma, perhaps through nuclear organization, while, in the pre-meiotic cells, simultaneously permit a separate mechanism that promotes pairing. Indeed, Christophorou et al. (also in this issue) show that pre-meiotic pairing is perturbed in the absence of meiosis-specific proteins such as components of the SC, suggesting that the mechanisms of pre-meiotic pairing cannot be entirely similar to that of somatic pairing.

Interestingly, we found that chromosomes maintain their peripheral localization even during the pre-meiotic 8-cell stage when homologs are fully aligned and continue to maintain this configuration into meiosis. Whether this localization is a significant aspect of pre-meiotic pairing will be of interest, as chromosome interactions with the nuclear envelope have been proposed to promote meiotic pairing in several organisms [54]–[57], as well as influence polytene pairing in Drosophila [58]. Regardless, our observations establish a distinction between the organization of paired chromosomes in pre-meiotic nuclei (peripheral localization) and that in somatic nuclei (internal localization) in Drosophila.

In closing, we return to the extraordinary degree of pairing that Drosophila and other Dipteran insects support in their soma. If homologous interactions can lead to negative outcomes, why do these organisms permit a near-organismal wide level of such interactions? One explanation is that somatic homolog interactions may, under some circumstances, confer advantages [12], [28], [34], [59]–[63] and, consistent with this, transient and localized instances of somatic homolog interactions have been documented or at least implicated in a wide variety of organisms, including mammals [1]–[7], [12], [63]–[65]. Indeed, in light of our discovery that the different tissues of Drosophila can have dramatically different levels of pairing it is possible that greater scrutiny of nonDipteran species will reveal many more instances of somatic pairing and, hence, evidence that somatic pairing is a widespread potential of genomes in general [12], [14], [43].

Materials and Methods

Drosophila strains

Drosophila stocks and crosses were maintained on a standard medium at 25°C. For wild-type, we used the y¹ w¹¹¹⁸ strain. To identify the BAM protein that was used to distinguish the pre-meiotic cyst stages, we crossed y¹ w¹¹¹⁸ to a strain carrying the transgene P(bamP-GFP) [44], a kind gift from Michael Buszcak (The University of Texas Southwestern Medical Center at Dallas).

Generation of FISH probes

Oligo probes for the 359, AACAC, and dodeca heterochromatic repeats [42], [66] were synthesized with either a 5′ Cy5 or Tye3 fluorescent dye by Integrated DNA Technologies (IDT). The design of the probe sequences were previously described [43] and are as follows: 359: GGGATCGTTAGCACTGGTAATTAGCTGC, AACAC: AACACAACACAACACAACACAACACAACACAACAC, and dodeca: ACGGGACCAGTACGG. Oligo probes were resuspended in 1×TE at 100 µM concentration and stored at −20°C.

Euchromatic probes 5A (4E2-5C10), 16E (16B3-17A2), 24D (24D1-24F1), 50D (50D1-53C7), 69C (69A1-69E6), and 100B (100B9-100D1) were designed and generated using the Oligopaint technology [40]. Briefly, a library of 7500 (24D and 100B), 10000 (5A, 16E, and 69C), and 25000 (50D) unique oligos (MYcroarray) were designed for amplification. Each library was amplified using a common 5′ Cy3-conjugated forward primer (5′-CGCTCGGTCTCCGTTCGTCTC) and unlabeled reverse primer (5′-GGGCTAGGTACAGGGTTCAGCgcaatg).

Antibodies

The antibodies and dilutions used were mouse anti-SXL (m18, Developmental Studies Hybridoma Bank [DSHB], 1∶10), rat anti-VASA (DSHB, 1∶300), mouse anti-Spectrin (DSHB 3A9, 1∶50), mouse anti-lamin (DSHB ADL84.12, 1∶100) and rabbit anti-GFP (Molecular Probes, 1∶300). The mouse anti-C(3)G (1A8-1G2, 1∶200) antibody was a gift from Scott Hawley (Stowers Institute, Kansas City, Missouri).

The secondary antibodies were DyLight 488 goat anti-rabbit (Jackson Labs) used at 1∶165, Cy3 labeled goat anti-rat (Jackson Labs) used at 1∶100 and DyLight 488 goat anti-mouse (Jackson Labs) used at 1∶100.

Immunofluorescence and FISH of Drosophila ovaries

Immunostaining was performed prior to FISH, using a modified protocol of [45]. Females (∼10–15 per experiment) were aged 3–4 days in the presence of males and were fed yeast paste overnight prior to dissection. Ovaries were isolated in PBS and immediately fixed for 10 min in 200 µl of PBS containing 4% formaldehyde and 0.5% Nonidet P-40, plus 600 µl Heptane. Fixed ovaries were then rinsed three times in PBT (PBS plus 0.2% Tween-20), and washed three times for 5 min in PBT. Prior to immunostaining, the ovaries were teased apart and blocked by incubating in PBT plus 1.5% BSA at room temperature for 1 hour. Primary antibodies were incubated at 4°C overnight in PBT. Three 20-min washes in PBT were performed prior to incubation with secondary antibodies at room temperature for 2 hours, followed by two 20-min washes in PBT and one 10-min wash in PBS.

For FISH, PBS buffer was replaced with 2×SSCT (0.3 M NaCl, 0.03 M NaCitrate, 0.1% Tween-20) by three quick washes. After washing, the ovaries were then gradually exchanged into 2×SSCT/50% formamide with 10-min washes in 2×SSCT/20% formamide, then in 2×SSCT/40% formamide, and then two washes in 2×SSCT/50% formamide. Ovaries were then allowed to settle and the 2×SSCT/50% formamide was removed prior to the addition of 36 µl of hybridization solution (2×SSCT, 50% formamide, 10% (w/v) dextran sulfate, RNase) and up to 4 µl of probe. For heterochromatic targets, 100 pmol of probe was added to the hybridization. For single-copy euchromatic targets, 200–400 pmol of Oligopaint probes were added to the hybridization. To preserve the nuclear structure, chromosomes were denatured at 78°C in a thermal cycler for 30 min followed by incubation overnight at 37°C in the dark. Following hybridization, we performed two 30-min washes of 2×SSCT/50% formamide at 37°C, followed by a 10-min wash in 2×SSCT/20% formamide at room temperature and three quick washes in 2×SSCT. After settling, excess 2×SSCT was removed and the ovaries were mounted in Slowfade mounting media with DAPI (Invitrogen).

Collection and fixation of Drosophila embryos

We collected 2.5 hour- and 14 hour-old embryos for 1 hour on apple juice plates and then aged them an additional 1.5 or 13 hours, respectively. 2.5 hours after egg lay (AEL) should capture embryos in the final 10 min of cell cycle 13 and the first 50 min of cell cycle 14. Due to the time spent manipulating embryos during the dechorionation step (see below), most embryos were aged ∼5–10 min longer before development was stopped during fixation. During imaging, embryos were also staged by the number and position of primordial germ cells, which are separated from the soma at the pole 2.5 hours AEL and encapsulated within the embryonic gonad 14 hours AEL (Figure 3B).

After collection, we dechorionated the embryos by submerging them in 50% bleach for 90 seconds, followed by a thorough wash in ddH₂O. For fixation, embryos were placed in PBS containing 4% formaldehyde, 0.5% Nonidet P-40, and 50 mM EGTA, plus 500 µl Heptane for 30 min. The aqueous phase was removed and replaced with 500 µl MeOH and mixed vigorously for 2 min. The embryos were allowed to settle and were washed two times in 100% MeOH and stored for up to a week at −20°C. Prior to immunostaining, the embryos were rehydrated in PBT. Immunostaining and FISH were then performed as described above for ovaries.

Microscopy and image analysis

All images were collected using a Zeiss LSM780 laser scanning confocal microscope with a 63×, N.A. 1.40 lens. We imaged whole germaria by collecting 200 nm optical sections through the entire tissue at 1024×1024 or 512×512 resolutions with a digital zoom of 3.0. The analysis of the images was performed by both 3D-image reconstruction and examining one section at a time using the Zeiss ZEN 2011 software. FISH foci were counted manually within each nucleus and the distance between the centers of allelic signals was measured using the Ortho – distance function, which permits length measurements in 3D space. 100% of nuclei examined in this study exhibited at least a single FISH signal, indicating high hybridization efficiency. Therefore, a single signal was considered two foci with an inter-signal distance of 0 µm. In some cases where noted, we normalized the inter-signal distances by the radius of the nucleus. In these cases, p values were determined by an unpaired t test.

Two homologs were considered paired if the distance between their focus centers was ≤0.8 µm or FISH produced a single signal. To determine the significance between paired states, p values were calculated by a two-tailed Fisher's exact test.

To image the pre-meiotic 2-, 4-, 8-, and 16-cell cysts, we focused on that region of the germarium identified by P[bamP-GFP] expression, set the upper and lower limits of the scanned region to capture the entirety of the cysts, and then scored those nuclei that were fully contained within the scanned region and were also unambiguously distinguished from other cell types. This strategy enabled us to score 93–100% of the cells in any chosen cyst.

To image germline cells in the embryo, we focused on that region identified by VASA expression, set the upper and lower limits of the scanned region to capture the majority of the germline cells, and then scored only those nuclei that were fully contained within the scanned region and were also unambiguously distinguished from somatic cells. This strategy enabled us to score the majority of germline cells in any chosen embryo. The somatic embryonic cells that were scored were those that were within the scanned region containing the scored germline cells.

Measuring nuclear volume

Nuclear envelopes were labeled with an anti-lamin antibody. Nuclear volumes were calculated based on the nuclear diameter using the equation V = 4/3πr³.

Measuring distance between nuclear envelope and FISH signals

Nuclear envelopes were labeled with an anti-lamin antibody. The ZEN software package was then used to measure the shortest distance between FISH signals and the nuclear envelope in 3D space. When two FISH signals were present in the nucleus, only the shortest distance of the two was scored. p values were determined by an unpaired t test.

Supporting Information

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