PIWI-interacting RNAs (piRNAs) are effectors of transposable element (TE) silencing in the reproductive apparatus. In Drosophila ovarian somatic cells, piRNAs arise from longer single-stranded RNA precursors that are processed in the cytoplasm presumably within the Yb-bodies. piRNA precursors encoded by the flamenco (flam) piRNA cluster accumulate in a single focus away from their sites of transcription. In this study, we identify the exportin complex containing Nxf1 and Nxt1 as required for flam precursor nuclear export. Together with components of the exon junction complex (EJC), it is necessary for the efficient transfer of flam precursors away from their site of transcription. Indeed, depletion of these components greatly affects flam intra-nuclear transit. Moreover, we show that Yb-body assembly is dependent on the nucleo-cytoplasmic export of flam transcripts. These results suggest that somatic piRNA precursors are thus required for the assembly of the cytoplasmic transposon silencing machinery.
Piwi-interacting RNAs (piRNAs) are a class of 23–29 nucleotide (nt) small RNAs that are expressed in animal gonads. In the metazoan germline, they play an important role in silencing transposable elements (TEs) and are thus critical for genome integrity1,2,3. In Drosophila, piRNAs originate from the processing of piRNA precursors transcribed from discrete genomic regions called piRNA clusters. piRNA clusters are enriched in TEs or their vestiges. In Drosophila melanogaster, their size ranges from 1 to a few hundred kb and they are almost exclusively located within or in close proximity to heterochromatic regions1. The ovarian somatic follicle cells preferentially express uni-strand piRNA clusters, transcribing one strand only. Current knowledge on piRNA cluster biology has been mostly acquired from studies conducted on flam locus, a uni-strand piRNA cluster active in the follicular cells4. flam is transcribed by the RNA polymerase II (RNA pol II) into a precursor that is similar to other RNA Pol II transcripts in basic RNA features5,6. Before being processed into piRNAs, the presumably long single-stranded transcript is spliced. Indeed, the flam precursor has been shown to contain a constitutive first exon. Several alternative splicings have also been reported5.
In the follicle cells, RNA precursors transcribed from piRNA clusters are first transferred to cytoplasmic perinuclear granules called Yb-bodies that have been reported to be major sites for piRNA biogenesis7,8. RNA precursors are then processed into primary piRNAs whose 5′ ends are defined by the endonucleolytic cleavage of Zucchini (Zuc) endonuclease9,10. They are loaded onto the PIWI clade protein, Piwi, and translocate to the nucleus where they elicit transcriptional silencing11,12,13,14,15,16.
In a previous study, Dennis et al.17 found that flam precursors channel through the nucleoplasm and first accumulate in a structure called Dot COM within the nucleus. This nuclear structure faces the cytoplasmic Yb-body and has been proposed to be a nuclear site of accumulation of piRNA precursors coming from various piRNA clusters before their export. This nuclear accumulation was not detected by Murota et al., who instead reported a cytoplasmic flam focus18. Whatever the positioning of this first accumulation of flam transcripts before processing, it is still unknown how such a transcript can be distinguished from other mRNAs and find its way to the Yb-bodies. A sequence crucial for piRNA production has been identified19. When a construct containing the 5′ end of flam fused to luciferase reporter gene is transfected into the ovarian somatic cells, luciferase RNA is processed via the primary processing machinery, giving rise to thousands of piRNAs. This prompted the authors to suggest that the 5′ end of flam transcript is a potential piRNA-trigger sequence. A cis-acting 100-nt-long fragment bound by Yb—a core component of Yb-bodies, has also been identified in the traffic jam (Tj) 3′ untranslated region that is sufficient for producing artificial piRNAs from unintegrated DNA20.
Several screens performed on Drosophila revealed factors required for the piRNA pathway21,22,23. The Nxf1/Tap and Nxt1/p15 export proteins as well as components of the exon junction complex (EJC) and UAP56 protein have emerged from these screens. Nxf1, a member of the NXF family of transport receptors, and its cofactor Nxt1, a low-molecular-weight NTF2-like protein, are thought to mediate export of the majority of cellular mRNAs24,25,26,27. Nxt1 enhances Nxf1-dependent RNA export by stimulating Nxf1 interactions with the nuclear pore complex28,29. Binding of the Nxf1–Nxt1 heterodimer to mRNAs is thought to be mediated by adaptor proteins. Consistently, EJC has been shown to facilitate the recruitment of Nxf1 to spliced mRNAs30. EJC is deposited onto mRNA upstream of exon–exon junctions concomitantly to splicing and remains associated during nuclear export25. It works as a platform for various transiently interacting factors, such as Nxf1–Nxt1 complex and the nuclear mRNA export factor UAP56, to link together several mRNA processes such as transport, translation or stability31,32,33,34. The two EJC core factors Mago and Tsunagi/Y14 (Tsu) as well as the EJC accessory proteins RnpS1 and Acinus (Acn) have been implicated in the piRNA pathway biology, their mutations leading to TE derepression21,23,35,36,37.
In the present study, we identify exportins-Nxt1 and Nxf1, EJC components—Mago, Tsu, RnpS1, Acn and UAP56 proteins—as factors required at different steps of flam nuclear traffic and export to the cytoplasm. We also demonstrate that export of piRNA precursors is the signal for the Yb-bodies to be assembled. In the follicle cells the flam cluster, which gives rise to most piRNAs, acts as a master locus for the formation of Yb-bodies.
Localization of piRNA precursors before processing
We first investigated the nucleo-cytoplasmic distribution of flam transcripts in more than 1,700 follicular cells. flam transcripts were revealed by in situ hybridization using the specific flam 508 RNA probe that recognizes a unique sequence of the flam locus17. An anti-lamin antibody was used to label the nuclear periphery and decipher the subcellular localization of flam transcripts in wild-type (WT) flies ISO1A. As previously reported, flam precursor transcripts were detected as a single focus per cell although a few cells displayed one or two foci at early stages of oogenesis17,18. This focus was always in close proximity to or at the nuclear periphery. 46% of cells (n=1,764) had a focus co-localizing with the lamin staining (Fig. 1, three middle panels and Fig. 2a, middle panel). In a few cases, flam staining seemed to extend through the lamin signal (Fig. 1, third and fourth panels). In all, 15% and 39% of cells had flam transcripts within the nucleus (a focus previously named Dot COM) and the cytoplasm, respectively (Fig. 1, left and right, respectively; Fig. 2a, left and right; Supplementary Movie 1). These findings suggest that most flam transcripts gather together and are likely visualized during their transfer from the nucleus to the cytoplasm.
Exportins Nxt1 and Nxf1 are involved in flam RNA export
To identify the proteins required for the transport of flam precursors to Yb-bodies, we looked for factors involved in the nuclear export of flam RNAs. Three genome-wide screens for identifying factors implicated in the piRNA pathway either in the germ line or in the somatic follicular cells have been performed21,22,23. Interestingly, knockdown of the central RNA export factors Nxf1 and Nxt1, which are involved in general mRNA export also prevents piRNA production and leads to TE derepression24,27,28. Nxt1 ovarian somatic knockdown (SKD) using the traffic-jam (tj)-Gal4 driver leads to female sterility and atrophic ovaries, which can however be dissected for analysis. The level of piwi and yb transcripts was examined in the SKD lines. No depletion was detected by quantitative PCR with reverse transcription (RT–qPCR) for both genes. Nevertheless, we found that depletion of Nxt1 and Nxf1 in ovarian somatic cells causes loss of Piwi nuclear localization and leads to TE derepression (Supplementary Fig. 1A,B)22. The decrease in Nxt1 and Nxf1 RNA level was analysed by RT–qPCR on whole ovaries. Because Nxt1 and Nxf1 are expressed both in the germline and in ovarian somatic cells, any decrease driven only in the follicle cells can be hardly detected (Supplementary Fig. 1C), even though the mutations cause defects in the piRNA pathway such as loss of Piwi nuclear localization and TE derepression (Supplementary Fig. 1A,B).
Nxt1- and Nxf1-SKD mutants show striking differences in flam precursor localization compared with WT flies. We observed a clear increase in the proportion of follicle cells with a nuclear accumulation of flam transcripts in Nxt1- and Nxf1-SKD (53%, n=1,527 and 27%, n=1,005, respectively) compared with WT ISO1A (15%, n=1,764) (Fig. 2a) correlated with a decrease in the proportion of cells with cytoplasmic accumulation (15% and 20%, respectively, versus 39% in WT). Moreover, the proportion of follicle cells with flam transcripts detected on the lamin signal was lower in Nxt1-SKD flies than in WT (respectively 31% and 46%) but not in Nxf1-SKD mutants (52%).
In addition, there was an overall increase in flam nuclear staining detected by larger foci in Nxt1-SKD, suggesting a nuclear retention of flam precursor in this exportin mutant (Fig. 2b and Supplementary Fig. 2). RT–qPCR experiments indicated that the level of flam transcripts in Nxt1-SKD ovaries was higher than in WT ovaries probably because flam precursors are not exported to the cytoplasm to be processed (Fig. 2c). Taken together, these data show that the Nxt1–Nxf1 complex is involved in the export of flam transcripts.
If flam precursors are not exported to the cytoplasm in Nxt1 or Nxf1-SKD mutants, we should expect that flam piRNA precursors cannot be processed into piRNAs. Thus, we sequenced small RNAs from mutant fly-ovaries and examined the level of piRNAs mapping to flam. We observed a large decrease in the levels of flam piRNAs in Nxt1-SKD flies compared with WT flies (5 versus 41 rpkm) (Fig. 2d). As expected, this decrease was observed all along the flam locus (Fig. 2e). The decrease in the level of flam piRNAs was low in Nxf1-SKD flies (37 rpkm) with no significant decrease along the locus (Fig. 2d,e).
We previously reported that flam transcripts are channelled within the nucleus from their site of transcription to the distant Dot COM, thus we decided to investigate whether Nxt1- and Nxf1-SKD also affect this intra-nuclear traffic of piRNA precursors. Double DNA/RNA FISH experiments were performed using flam 508 RNA probe and a DNA probe made from the DIP1 gene, a unique genomic sequence flanking the flam locus. As previously reported, two distinct foci were detected in 93% of the 346 WT ISO1A nuclei examined due to the accumulation of flam transcripts away from the genomic flam piRNA cluster. Surprisingly, in Nxt1- and Nxf1-SKD flies, flam RNA and DNA co-localized in 43% and 38% of 438 and 532 nuclei examined, respectively (Fig. 2f,g and Supplementary Fig. 3).
Thus, the Nxt1–Nxf1 complex is required for the efficient transfer of flam precursors away from their site of transcription.
EJC is required to transfer flam transcripts to Dot COM
Exportins Nxf1 and Nxt1 are transiently interacting factors of EJC that associates with transcripts concomitantly to splicing30. Together with Nxf1 and Nxt1 proteins, the two core EJC factors Mago and Tsu and the EJC accessory proteins RnpS1 and Acn have been involved in the piRNA pathway biology, with their mutation leading to TE derepression21,23,35,36,37. EJC works as a platform linking RNA splicing and export, and facilitates the recruitment of Nxf1 to spliced mRNAs30. We investigated whether components of EJC could, like the Nxt1–Nxf1 complex, play a role in the export and/or intra-nuclear traffic of flam transcripts. We also tested UAP56 protein, a putative RNA helicase known to transiently interact with EJC that is required for spliceosome assembly23,38,39. The sub-cellular localization of flam transcripts was assessed in SKD flies depleted for Mago, RnpS1, Tsu, Acn and UAP56.
In preliminary experiments, we performed four tests. First, we tested Piwi localization in the depleted lines. We found that Piwi is absent from the nucleus of these SKD lines with two exceptions, Mago- and UAP56-SKD flies, which have a nuclear Piwi signal either faint or comparable to that of WT flies, respectively (Fig. 3a). Second, we examined the level of the corresponding knocked-down transcripts in the SKD lines. As reported above, because these genes are also expressed in the germline, a depletion was only observed in Tsu- and UAP56-SKD lines, while depletion was hardly detected in Mago- and Rnps1-SKD and not in Acn-SKD (Supplementary Fig. 4A). These variations can potentially be attributed to differences in the expression of these genes within the germline. Thus, we further verified that the silencing exerted on somatic TEs was lost in all these mutants (Supplementary Fig. 4B). Third, since splicing of some mRNAs is impeded in EJC mutants36,37, we performed RT–PCR using primers in flam exon 1 and exon 2 to verify whether flam splicing is affected. We found that flam intron 1 is correctly spliced in all these SKD lines (Fig. 3b,c). Fourth, we analysed by RT–qPCR the impact of Mago- and RnpS1-SKD on the expression of major genes involved in the somatic piRNA pathway like piwi, armitage (armi), maelstrom (mael) or yb (Supplementary Fig. 5). We found that the expression of none of these genes is affected in these mutants except piwi whose expression decreases in Rnps1-depleted line as earlier reported36,37 (see Discussion).
Immuno-FISH experiments were then performed to examine flam export in SKD mutants for EJC components and UAP56. As seen in Fig. 3d and Supplementary Fig. 6, flam transcripts accumulate in a single focus in all depleted lines. In addition, the proportion of cells having cytoplasmic, transmembrane and nuclear accumulation of flam transcripts in mutant lines was similar in SKD lines and WT (Fig. 3e). Overall, these data indicate that in EJC and UAP56-depleted lines, flam transcripts are properly spliced and exported to the cytoplasm.
To assess piRNA production, we sequenced ovarian small RNAs from Mago- and RnpS1-SKD lines. piRNAs mapping to flam were detected at a similar level in Mago-SKD and WT flies (Fig. 4a,b). Thus, although somatic TE silencing is altered in Mago-depleted flies, flam precursors nevertheless retain the ability to be processed into piRNAs. Surprisingly, a distinct reduction in the production of flam piRNAs was observed in RnpS1-depleted flies (Fig. 4a,b). Since the export of piRNA precursors appeared to be unaffected (Fig. 3d,e), this suggests that an additional step for the production/stability of piRNAs is missing.
To examine the intra-nuclear traffic of flam piRNA precursors, the relative localization of nuclear flam transcripts to flam genomic locus was analysed by double DNA/RNA FISH. Strikingly, an increase in the co-localization of flam precursor with its genomic site of transcription was observed (Fig. 4c,d and Supplementary Fig. 7). In Mago- and RnpS1-depleted flies, DNA and RNA co-localize in 40% (n=553) and 38% (n=533) of follicle cells, respectively, while flam transcripts are detected at their site of transcription in only 7% (n=346) of WT cells. To a lesser extent 16% (n=430), of follicle cells have a co-localization between flam RNA and DNA in Tsu-depleted line (Fig. 4d). No significant difference was found in Acn- and UAP56-depleted lines compared with WT. However, in all EJC-depleted lines, including Acn and UAP56 mutant lines, the transfer of flam transcripts to Dot COM appears to be affected. Indeed, in a few cells, we also observed two distinct Dot COMs, neither of which co-localized with flam DNA (Fig. 4e and Supplementary Fig. 8), suggesting that gathering of flam transcripts during the transfer from their site of transcription to a single focus of accumulation is affected in all these mutant lines.
Altogether, these results indicate that EJC components are required to transfer flam transcripts from their site of transcription to the distant nuclear Dot COM site. They also show that flam transcripts reach a single site of accumulation.
Export of flam precursors is required for Yb-body formation
Nuclear Dot COM is often juxtaposed with the cytoplasmic Yb-body17. In Nxt1-SKD mutants, flam transcripts are neither shuttled from their site of transcription to Dot COM nor exported to the cytoplasm. To a lesser extent, the transfer of flam precursors to Dot COM is also affected in Nxf1-SKD. We sought to examine the position of the Yb-bodies in these two SKD lines. Immunofluorescence experiments were performed using anti-Armi and anti-Yb antibodies, which are two major constituents of Yb-bodies. Strikingly, very few Y-bodies were visualized in Nxt1-SKD mutants. Only 26% (n=1,333) of follicle cells, still harboured Yb-bodies compared with 63% (n=1,401) in WT flies. Instead, Armi and Yb proteins were dispersed throughout the cytoplasm of follicular cells giving rise to a diffuse cytoplasmic signal (Fig. 5a,b and Supplementary Fig. 9A). In Nxf1-SKD flies, a faint Armi cytoplasmic staining was observed. Yb-bodies were also detected but they looked smaller than in WT. These data suggest that either export or intra-nuclear traffic of flam precursors could be required for Yb-body assembly.
In knockdown lines for EJC components, the intra-nuclear traffic of flam is affected but not its export. We first investigated whether Yb-body formation is altered in Mago- and RnpS1-SKD lines. Follicle cells having at least one Yb-body were found in a similar proportion to that in WT flies (Fig. 5c,d and Supplementary Fig. 9B). No visible cytoplasmic diffuse Armi or Yb signal was registered. A correct assembly of Yb-bodies has been previously reported in other EJC mutants37. These results indicate that it is the export of flam transcripts and not their intra-nuclear traffic that is the signal for Yb-body assembly.
Immuno-FISH experiments were then used to examine the position of Yb-bodies in Mago-, RnpS1-, Tsu-, Acn- and UAP56-SKD lines. They showed that cytoplasmic Yb-bodies are juxtaposed to nuclear flam transcripts (Fig. 6a,b and Supplementary Fig. 10). Since the nuclear traffic of flam transcripts is disrupted in these mutants, it is expected that Yb-bodies are then juxtaposed to flam transcription site. By combining DNA FISH and immunofluorescence, we confirmed that a higher proportion of Yb-bodies is juxtaposed to the flam genomic locus in RnpS1-SKD line compared with WT (Fig. 6c,d). Interestingly, in a few cells displaying two Dot COMs, two Yb-bodies were assembled, each of them facing one Dot COM (Fig. 6e and Supplementary Fig. 11). Taken together, these data indicate that Yb-bodies assemble at the site where accumulated flam precursors are exported irrespective of whether transcripts are channelled away or not from their transcription site. They further indicate that flam precursor traffic within the nucleus occurs in a process that is upstream of Yb-body formation.
flam is the major piRNA cluster expressed in ovarian somatic cells. Other piRNA clusters are expressed in these cells but they weakly participate in the production of piRNAs1. We investigated whether transcripts originating from other piRNA clusters are sufficient to induce the assembly of Yb-bodies. We used the flam BG02658 allele (flamBG), which, owing to a P-transgene inserted upstream of flam transcription start site, produces no flam transcripts40. Homozygous mutant ovaries are small and atrophic with very few egg chambers. However, we were able to examine a few egg chambers in which an epithelium of follicle cells was correctly formed. Mutant follicle cells have smaller, fainter and many more Armi foci than do WT cells. In addition, we observed a diffuse cytoplasmic staining in homozygous flamBG, similar to what was seen in Nxt1-SKD follicle cells, suggesting that a fraction of Armi protein fails to accumulate in foci (Fig. 6f). These data indicate that flam piRNA cluster acts as a master locus in ovarian follicle cells for Yb-body assembly.
In this work, we examined how the piRNA precursors are transferred from their site of transcription to the cytoplasmic structure where they are processed into primary piRNAs. We report that, in the follicle cells of Drosophila ovaries, EJC components and their associated proteins Nxf1, Nxt1 and UAP56 play a crucial role in this process that displays three steps: recognition of the precursor, transfer through the nucleoplasm away from the DNA locus and export to the cytoplasm. We further show that export of flam transcripts is required for the presumed processing structure called the Yb-body to assemble in the cytoplasm.
We found that the traffic of flam piRNA precursors within the nucleus from the DNA locus to a distal nuclear structure previously called Dot COM depends on EJC factors Mago, RnpS1 and Tsu and on exportins Nxt1 and Nxf1.These data argue that binding of EJC and export proteins occurs shortly before or after release of flam precursors from their site of transcription and provide a link between flam precursor splicing and its downstream nuclear transfer to Dot COM. At present, we do not know whether interaction between the flam precursor and these factors is direct or indirect. EJC components may each bind flam precursor directly and independently. Alternatively, some may bind directly, whereas others may only associate indirectly through interactions within the complex. It is also possible that these interactions occur with other yet unknown factors. Moreover, we cannot exclude that through a more general effect on mRNA processing and transport, EJC mutants may indirectly affect flam export and the piRNA pathway. However, it has been verified that depletion of each of these EJC components had no significant impact on the level of transcripts of genes involved in the somatic piRNA pathway except for piwi whose transcripts level decreases in RnpS1-SKD (Supplementary Fig. 5A and ref. 36).
Nxf1 and Nxt1 are involved in flam export (Fig. 2a). However, depletion of Nxf1 has a limited impact on piRNA production. It is possible that the redundancy which has been reported between export components binding nuclear pore complex may compensate depletion of Nxf1 (refs 41, 42). Alternatively, in our SKD mutant, a residual Nxf1 function could be sufficient to allow the export of enough flam precursors that are processed to an almost WT amount of piRNAs (37 and 41 rpkm, respectively) (Fig. 2e). Nxt1 plays an essential role in the export of piRNA precursors in follicle cells. Several studies have reported the ability of Nxt1 to mediate nuclear mRNA export by controlling the interaction of Nxf1 with components of the nuclear pore29,43. Our data further extends the critical importance of Nxt1 to this non-coding RNA export.
Components of the EJC assume different functions to connect nuclear pre-mRNA maturation to mRNA fate. Their individual functions certainly affect different steps in the flam transfer to the cytoplasm. Mago and Tsu are known to form a heterodimer required for a tight binding of EJC to the targeted RNAs30. RnpS1 and Acn have been implicated in mRNA quality control, pre-mRNA splicing and transcriptional regulation44. UAP56 is involved in splicing and mRNA export45. However, we could hardly attribute specific roles to these EJC components in the nuclear traffic of flam. Their mutation does affect neither flam transcription, nor splicing, nor its nucleo-cytoplasmic export. The only step that is affected in all mutants is the intra-nuclear traffic of flam transcripts and/or, occasionally, their gathering to a single focus of accumulation (Fig. 4e and Supplementary Fig. 8). Differences depending on the depleted gene were nonetheless observed. First the intra-nuclear traffic of flam from the site of transcription to Dot COM is greatly affected in Mago- and Rnsp1-SKD and to a less extend in Tsu mutant. Instead, Acn-, UAP56-, as well as Tsu-SKD appear to affect the gathering of flam precursors into a single focus. Second, flam processing into piRNAs is highly decreased in RnpS1- or Tsu-depleted flies but not in Mago-SKD (Fig. 4a,b and ref. 22) or UAP56 mutants38. To better understand the interactions and the role played by each of these factors on flam precursor processing, it will be important to find the temporal sequence of binding, if binding to RNA is direct and if some of the components bind the potential piRNA-trigger sequence that is crucial for piRNA production19.
EJC mutants have been reported to affect mRNA splicing. Notably, excision of the piwi fourth intron is impaired and the level of Piwi protein reduced. The decrease in piRNA level observed in RnpS1 mutant could be due to the loss of Piwi protein. In this case, processed piRNAs would not be able to be loaded onto Piwi and would then be degraded. Why it is not observed in other EJC mutants is not known but in Mago and UAP56 mutants Piwi transcription and splicing is poorly affected36,37,38 and Piwi protein is detectable within the nucleus (Fig. 3a). This small amount of WT Piwi could be sufficient to stabilize piRNAs. These data raise an important question. Why are Mago, Acn and Tsu mutants unable to silence somatic TEs if piRNAs are normally produced? Several hypotheses can be proposed. First, unknown proteins whose mRNA splicing is also affected by the mutations could be required to produce functional piRNAs or to silenced TE at the transcriptional level. Second, the traffic of flam precursors away from their transcription site before leaving the nucleus may be required for the piRNAs to become functional. This hypothesis is consistent with the known role of EJC proteins to mark RNAs for downstream stability; However it is still an open question whether the defect in TE silencing observed in EJC SKD is directly or indirectly connected to intranuclear trafficking of flam.
Unlike somatic cells, germline has evolved a mechanism that inhibits splicing of the nascent piRNA transcript39. piRNA clusters expressed in the germline are preferentially dual-strand clusters based on transcription orientation occurring from both strands. The RDC complex composed of Rhino, Deadlock, Cutoff is required for the non-canonical transcription of these dual-strand piRNA clusters and involves 5′ end protection of nascent RNAs and suppression of transcription termination. It was speculated that stalled splicing due to RDC and UAP56 differentiates these piRNA precursors from mRNAs39,46,47. Then, our study underlines that the non-canonical transcription of dual-strand piRNA clusters in the germline and the canonical transcription of uni-strand clusters in the follicle cells engage different processes both leading to piRNA biogenesis.
Overall, it can be anticipated that components of EJC and exportin pathways that are well conserved throughout eukaryotes fully participate in the defence system protecting genomes from TE invasions.
When flam precursors are channelled within the nucleus to Dot COM, Yb-bodies are detected facing Dot COM. If this intra-nuclear traffic is blocked as in EJC mutants, in which flam precursors are exported into the cytoplasm close to their site of transcription, then Yb-bodies are juxtaposed to the flam genomic locus. Interestingly, when two flam foci are observed in EJC mutants, each of them face one Dot COM, confirming that wherever flam transcripts are exported, a Yb-body is always detected in close proximity. Moreover, when flam piRNA cluster is not transcribed in flies carrying the flamBG allele, Yb-body formation is greatly affected. A clear dispersed Armi cytoplasmic staining suggests that a large part of Armi protein fails to accumulate in one spot. flam is a very specific piRNA cluster as it produces the largest amount of piRNAs in follicle cells. We here provide evidence that it also acts as a master locus for Yb-body assembly.
Interestingly, in the Drosophila germline, an extrinsic control of nuage assembly and function exerted by nuclear components has also been reported38. Like Yb-bodies in the somatic lineage, nuage is the cytoplasmic structure in the germline where piRNA biogenesis is likely to occur. Discrete nuclear foci corresponding to germline piRNA cluster transcripts bound by Rhino and UAP56 proteins have been observed juxtaposed to the cytoplasmic nuage. When mutations affect UAP56, the nuage assembly is disrupted, revealing an upstream requirement of UAP56. Zhang et al. proposed that Rhino and UAP56 are connected to the nuage via the nuclear pore complex that could therefore trigger release of cluster transcripts in the nuage. A nuclear envelope-spanning machinery would then be required for piRNA biogenesis. Like in the germline, we found that Yb-body assembly requires flam export as an extrinsic control coming from the nucleus. However, as opposed to the germline, UAP56 is not required for Yb-body assembly since its mutants do not disrupt Yb-bodies (Fig. 6a). It is possible that Nxt1 plays a key role in this process by stimulating interactions of exportins with components of the nuclear pore. Further insight into the machinery spanning the nuclear envelope is necessary to enlighten the whole mechanism that will result in the precursor export through the nuclear membrane.
All flies were kept at 20 °C. Strains ISO1A, W1118, BG/FM4 and traffic jam (tj)-GAL4/CyO came from the collection of the GReD. nxt1 [VDRC GD49602] strain was obtained from Vienna Drosophila Resource Center. nxf1/sbr , mago , rnpS1 , tsu , acn  and uap56/hel25E  strains were obtained from the Bloomington Drosophila Stock Center.
In situ hybridization
The DNA fragment to prepare the specific flam 508 probe to detect flam transcripts was PCR amplified from the ISO1A line using primers 5′-ATTCTCCTTTCTCAGGATGC-3′ and 5′-GCATTGCTACCTTACGTTTC-3′ and cloned into pGEMT easy vector.
Riboprobe was synthesized by digestion of pGEMT easy plasmids with NcoI or SpeI enzyme, followed by in vitro transcription using Sp6 or T7 polymerase and digoxygenin labelled UTP (Roche), DNAse I treatment and purification.
DNA probe are made of eleven PCR amplifications (Supplementary Table 1) labelled with digoxigenin using nick translation kit (Roche).
RNA FISH was performed on ovaries from 2- to 4-days-old flies dissected in 0.2% Tween 20, phosphate-buffered saline (PBT). Ovaries were fixed with 4% formaldehyde/PBT at room temperature (RT) for 30 min, rinsed three times with PBT, post-fixed 10 min in 4% formaldehyde/PBT and washed in PBT. After permeabilization 1 h in PBS-0.3% Triton, prehybridization was performed as follow: 10 min HYB- (Formamide 50%, SSC 5 × , Tween 0.02%)/PBT 1:1, 10 min HYB-, 1 h HYB+ (HYB- with yeast tRNA 0.5 mg ml−1, heparin 0.25 mg ml−1) at 60 °C. Ovaries were hybridized overnight at 60 °C with 1 μg riboprobe. Ovaries were then rinsed 20 min in HYB- and in HYB-/PBT 1:1 at 60 °C then four times in PBT at RT before blocking 1 h at RT in TNB 0.3% triton (Perkin-Elmer TSA kit) and immunodetection 1 h 30 min at RT with anti-digoxigenin-HRP (11 207 733 910, Roche, 1:200 dilution) in TNB 0.2% tween. Ovaries were rinsed three times in PBT, incubated 10 min with TSA-Cy3 in amplification diluent (Perkin-Elmer, 1:50 dilution), and rinsed.
When coupled to immunofluorescence, RNA staining was followed by incubation with mouse anti-lamin antibody (ADL67-10, Hybridoma, 1:300 dilution) and goat anti-Armi antibody (sc-34564, Santa Cruz, 1:250 dilution). Secondary antibodies coupled to Cy3 or Alexa-488 were used.
For DNA/RNA in situ hybridization, RNA staining was followed by treatment with 200 μg ml−1 RNase A for 2 h after which the ovaries were transferred to FISH hybridization buffer containing 50% formamide, 4 × SSC, 0.1% Tween 20, 0.1 M NaH2PO4. DNA was denatured for 15 min at 80 °C and hybridization with DNA probe was carried out O/N at 37 °C. After washes, the ovaries were first incubated with glycine 0.1 M–0.1% Tween HCL pH 2.2 before washes and DNA staining. DNA staining was performed by blocking for 1 h at RT in TNB, immuno-detection for 1 h 30 min at RT with anti-Digoxigenin-HRP (11 207 733 910, Roche, 1:200 dilution) in TNB 0.3% Triton, washes three times in PBT, incubation for 10 min with TSA-Cy3 in amplification diluent (Perkin-Elmer, 1:25 dilution), rinsing three times in PBT and staining with Hoescht.
For DNA FISH coupled to immunofluorescence, ovaries from 2- to 4-day-old flies were dissected in PBT (PBS-0.2% Tween) fixed with 4% formaldehyde/PBT at RT for 30 min, rinsed three times with PBT, post fixed for 10 min with 4% formaldehyde/PBT at RT and rinsed in PBT. The ovaries were then permeabilized for 1 h in PBS-0.3% Triton, rinsed three times with PBT and incubated for 1 h in TNB (Perkin-Elmer TSA kit) 0.3% Triton prior to staining with mouse anti-Armi antibody (kindly provided by M. Siomi). Incubation with secondary antibodies coupled to Cy3, Cy-5 or Alexa-488 was followed by treatment with 200 μg ml−1 RNase A for 2 h. The ovaries were then transferred to FISH hybridization buffer containing 50% formamide, 4 × SSC, 0.1% Tween 20, 0.1 M NaH2PO4. DNA was denatured for 15 min at 80 °C and hybridization with DNA probe was carried out O/N at 37 °C. After washes, the ovaries were treated for DNA staining.
Ovaries from 2- to 4-day-old flies were dissected in PBT (PBS-0.2% Tween) fixed with 4% formaldehyde/PBT at RT for 20 min, rinsed three times with PBT, incubated for 1 h in PBS-0.3% Triton, rinsed three times with PBT and incubated for 1 h in TNB (Perkin-Elmer TSA kit) 0.3% Triton prior to staining with mouse anti-lamin antibody (ADL67-10, Hybridoma, 1:300 dilution), goat anti-Armi antibody (sc-34564, Santa Cruz, 1:250), rabbit anti-Yb antibody (kindly provided by J. Brennecke, 1:1,000 dilution) or rabbit anti-Piwi antibody (sc-98264, Santa Cruz, 1:500 dilution). Secondary antibodies coupled to Cy3, Cy-5 or Alexa-488 were used. Three-dimensional images were acquired on Leica SP5 and Leica SP8 confocal microscopes using a × 40 objective.
Total RNA was isolated from 10 pairs of ovaries from 2- to 4-day-old flies with Trizol (Ambion). Following DNAse I treatment, cDNA was prepared from 1 μg RNA by random priming of total RNA using Superscript IV Reverse Transcriptase (ThermoFisher Scientific).
PCR were performed with Phusion DNA polymerase (New England Biolabs) using e1F 5′-AGTTGCTTTATGACGCCGGGC-3′ and e2R 5′-GCTAGGAAGCTAATTGATCAATGACAAC-3′ primers.
qPCR were performed using standard techniques. All experiments were conducted in biological triplicates with technical triplicates. Relative RNA levels were normalized to rp49 levels. Fold enrichments were calculated in comparison with RNA levels obtained from WT ISO1A line. Primer sequences for RT–qPCR analyses are listed in Supplementary Table 2.
Small RNA sequencing
Total RNA was isolated from 10 pairs of ovaries from 2- to 4-day-old flies with Trizol (Ambion). Deep sequencing of 18–30 nt small RNAs was performed by Fasteris S.A. (Geneva/CH) on an Illumina Hi-Seq 2500. Illumina reads were matched to release 6 of the Drosophila genome. Only reads mapping uniquely to the genome were used for further analysis. All libraries were normalized based on the number of mapped reads. Size profile for flam piRNA cluster was obtained by extracting the abundance and read length of 23–29 nt sequences uniquely matching to this locus.
All Illumina data sets that support the findings of this study have been deposited at GEO with the accession codes: BioProject ID PRJNA348903. The data that support the findings of this study are available from the corresponding author upon reasonable request.
How to cite this article: Dennis, C. et al. Export of piRNA precursors by EJC triggers assembly of cytoplasmic Yb-body in Drosophila. Nat. Commun. 7, 13739 doi: 10.1038/ncomms13739 (2016).
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This work was supported by grants from the Agence National pour la Recherche (ANR—Plastisipi project). E.B. and A.S. received a grant from the Région Auvergne and Université d'Auvergne, respectively. We are grateful to R. Pogorelcnik and P. Pouchin for the pipeline used for the small RNA analysis, and J. Brennecke and M. Siomi for antibodies.
Transcripts from Dot COM localize within the nucleus, close to the nuclear membrane. Movie of 3D imaging of ovarian follicle cells stained with flam 508 riboprobe (red) and anti-lamin antibody (green).
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