Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

The Tudor domain protein Tapas, a homolog of the vertebrate Tdrd7, functions in the piRNA pathway to regulate retrotransposons in germline of Drosophila melanogaster

BMC Biology volume 12, Article number: 61 (2014) Cite this article

Abstract

Background

Piwi-interacting RNAs (piRNAs) are a special class of small RNAs that provide defense against transposable elements in animal germline cells. In Drosophila, germline piRNAs are thought to be processed at a unique perinuclear structure, the nuage, that houses piRNA pathway proteins including the Piwi clade of Argonaute family proteins, along with several Tudor domain proteins, RNA helicases and nucleases. We previously demonstrated that Tudor domain protein Tejas (Tej), an ortholog of vertebrate Tdrd5, is an important component of the piRNA pathway.

Results

In the current study, we identified the paralog of the Drosophila tej gene, tapas (tap), which is an ortholog of vertebrate Tdrd7. Like Tej, Tap is localized at the nuage. Alone, tap loss leads to a mild increase in transposon expression and decrease in piRNAs targeting transposons expressed in the germline. The tap gene genetically interacts with other piRNA pathway genes and we also show that Tap physically interacts with piRNA pathway components, such as Piwi family proteins Aubergine and Argonaute3 and the RNA helicases Spindle-E and Vasa. Together with tej, tap is required for survival of germline cells during early stages and for polarity formation. We further observed that loss of tej and tap together results in more severe defects in the piRNA pathway in germline cells compared to single mutants: the double-mutant ovaries exhibit mis-localization of piRNA pathway components and significantly greater reduction of piRNAs against transposons predominantly expressed in germline compared to single mutants. The single or double mutants did not have any reduction in piRNAs mapping to transposons predominantly expressed in gonadal somatic cells or those derived from unidirectional clusters such as flamenco. Consistently, the loss of both tej and tap function resulted in mis-localization of Piwi in germline cells, whereas Piwi remained localized to the nucleus in somatic cells.

Conclusions

Our observations suggest that tej and tap work together for germline maintenance. tej and tap also function in a synergistic manner to maintain examined piRNA components at the perinuclear nuage and for piRNA production in Drosophila germline cells.

Background

Animal genomes have been invaded by a variety of transposons that propagate by populating the germline genome [1]. To combat the deleterious effects of invading transposons in the germline cells, host genomes have co-evolved an elegant RNA-based defense mechanism involving the Piwi-interacting RNAs (piRNAs) [2]. The piRNAs have been reported in many animals, such as Drosophila, rat, mouse and zebrafish [3]-[10]. In Drosophila, piRNA biogenesis involves two pathways: primary and secondary processing [9],[10]. Primary processing, which involves Piwi, occurs in both somatic and germline cells of gonads. In this process, precursor transcripts from genomic clusters, which are specialized sites harboring fragmented transposons copies incapable of mobilization, are randomly processed into 23- to 29-nucleotide piRNAs that are in antisense orientation to the transposons. Secondary processing is a feed-forward loop that is also termed the ping-pong cycle [6],[7]. The ping-pong cycle occurs only in germline cells and involves the two other Piwi family proteins, Aub and Ago3 (reviewed in [1]). This process is hypothesized to involve the cutting of transposon transcripts by Piwi/Aub-bound antisense piRNAs and the loading of resultant sense piRNAs onto Ago3. The Ago3 complex then cleaves antisense cluster transcripts for further processing into antisense piRNAs [6],[7].

Aub and Ago3, along with many other proteins that are required for piRNA production in germline cells across species, localize to the nuage (`cloud' in French), a conserved perinuclear structure found in animal germline cells [2],[11],[12]. The evolutionarily conserved localization of piRNA pathway proteins makes the nuage a potential compartmentalized piRNA processing site in germline cells [2]. A majority of conserved nuage components contain Tudor domains, which bind symmetrically di-methylated arginine residues of Piwi family proteins and participate in the piRNA pathway [13]-[15]. We previously identified Tejas (Tej), a Tudor domain protein, as a germline piRNA pathway component [16]. The gene tej is required for transposon repression and localization of several piRNA pathway components to nuage, and Tej also physically interacts with the piRNA components Ago3, Aub, SpnE and Vas.

Here, we report the identification and characterization of tapas (which means `heat' in Sanskrit, hereafter abbreviated as tap), a paralog of Drosophila tej and an ortholog of vertebrate Tdrd7. Tap is predominantly expressed in the germline cells and co-localizes with other piRNA pathway components. The gene tap genetically interacts with other piRNA pathway components, and Tap protein also physically interacts with the piRNA pathway components Ago3, Aub, SpnE and Va. Loss of tap leads to a milder derepression of a subset of retroelements that are repressed in the germline and a reduction in piRNAs mapping to them. However, when combined with the loss of tej function, the double mutants show loss of germline cells and a greater reduction in piRNA with more severe derepression of retrotransposons. Our results suggest that Tap functions synergistically with Tej in a complex to promote proper germline development and piRNA production.

Results

tap encodes a conserved Tudor domain protein that localizes to the nuage

We previously reported a Tudor domain protein Tej as a germline piRNA pathway component required for transposons repression and nuage localization of several other piRNA pathway components [16]. The Drosophila gene CG8920 encodes its paralog, Tap. The orthologs of Tap and Tej, Tdrd7 and Tdrd5 respectively, are found in other animals, such as human, mouse, rat and zebrafish, and localize to the nuage [11],[17]-[21]. Tap as well as Tdrd7 has three Tudor domains and a Tejas/Lotus domain (Figure 1A; [16],[22],[23]). Given its similarity with Tej, we addressed if Tap, like many other Tudor domain proteins, functions in the piRNA pathway in the germline [15],[16],[24]-[27].

Figure 1
figure 1

tap encodes a Tudor domain protein and localizes to the nuage. (A) Schematic representation of the Tap and Tej proteins and their respective mouse orthologs, TDRD7 and TDRD5. Tap has three Tudor domains and a Tejas/Lotus domain in the C- and N-termini, respectively. (B) Schematic representation of the tap genomic locus. The tap gene is predicted to be transcribed in to five isoforms. The area between the green lines represents the deleted region in tap125. (C) RT-PCR showing a truncated transcript in tap125 ovaries. Primers 1, 2 and 3, which were used for RT-PCR, are indicated in (B) by the red arrowheads at the top. (D) Western blotting analysis using anti-Tap antibody detected a single band of approximately 110 KDa, which is closer to the predicted Tap size. The antibody could not detect a band at same position in tap125-mutant ovaries. (E,F) Ovaries immunostained for Tap (green) and Vas (red). (E) Tap localizes to the perinuclear nuage with Vas. Scale bar =20 μm. Insets show a closer view of a single nurse cell nucleus. (F) Tap was undetectable in tap125-mutant ovaries. Scale bar =5 μm.

Full size image

To analyze tap function, we generated a deletion mutant through imprecise excision of a P-element, EY02725, inserted within an intron of the tap gene. The resulting allele, tap125, lost a 1.33-kb genomic region encompassing a portion of the longest common exon shared by all putative tap isoforms (Figure 1B). RT-PCR confirmed a truncation of the tap transcript in tap125-mutant ovaries (Figure 1C). Western blotting with anti-Tap antibody detected a band corresponding to the predicted size of Tap protein, which was absent in tap125-mutant ovaries (Figure 1D), indicating tap125 is a loss-of-function allele. Similar to its paralog Tej, Tap expression was observed only in germline cells and localized to the perinuclear foci in all germline cells except oocytes (Figure 1E,F; [16]). Immunostaining showed that most of the Tap foci co-localized with well-known nuage components, Vas and Tej (Figure 1E,F; Additional file 1: Figure S1A; [16],[28]), though there were few distinct foci of each of those, suggesting that Tap is a nuage component. The Myc-tagged Tap protein expressed from a transgene also co-localized with Vas at the perinuclear nuage when expressed by the germline driver nanosGAL4 (Additional file 1: Figure S1B). Unlike Vas, however, endogenous Tap and Myc-Tap localized only to the nuage and not to the pole plasm (Additional file 1: Figure S1C; [29],[30]). The perinuclear localization of Tap was undetectable in tap125 ovaries (Figure 1F), which confirms the specificity of the antibody and the perinuclear localization of Tap. Nuage localization of Tap was further confirmed by examining a protein trap line, CC00825, expressing GFP-Tap (Additional file 1: Figure S1D; [31]).

tap likely shares a synergistic functional relationship with its ortholog tej for the germline development

The female and male homozygotes of tap125 as well as trans-heterozygotes, tap125 over Df(2R)BSC19 uncovering the tap locus, were viable and fertile, indicating that tap function is dispensable for Drosophila viability and fertility under laboratory conditions. Although Tap localized with Vas at nuage, tap125 did not display any of the severe phenotypes observed in other mutants of piRNA pathway components that localize to the nuage, such as sterility, defective karyosome formation, DNA double-strand breaks and failure in polarity formation (reviewed in [2]). The similarity in tej and tap gene structures prompted us to examine the possibility that these two genes have a functional relationship. To assess this possibility, we generated a tej-tap double mutant by recombining tej48-5and tap125alleles. The double-mutant females were sterile and males were fertile only for the first few days after eclosion, whereas both tej125 and tap48-5 single-mutant males were fertile [16]. The tej125-tap48-5 double-mutant gonads showed severe degeneration: by seven days post eclosion (dpe) most of the double-mutant ovaries became atrophic and were very small compared to the heterozygote control, whereas both tej48-5 and tap125 single-mutant ovaries were visibly similar in size compared to the controls (Additional file 1: Figure S2A). The degeneration of double-mutant ovaries usually started after three dpe; most of the four to six dpe ovarioles showed germaria containing very few germline cells attached to very late stage egg chambers (Figure 2A). A very small percentage of two-dpe double-mutant ovaries showed this phenotype. A similar degeneration of germline cells was also observed in the male gonads (Additional file 1: Figure S2C). Hence in subsequent experiments, unless otherwise noted, we analyzed one- to two-dpe double-mutant flies to avoid any defects that may have been caused by gonad degeneration. Our data suggest that the double mutants may have defects in the maintenance and/or division and differentiation of germline stem cells (GSCs).

Figure 2
figure 2

The tej48-5-tap125double mutant exhibits more severe defects during oogenesis. (A) DAPI staining of tej48-5-tap125 double-mutant ovarioles shows defects in the germline development. (B) Immunostaining with α-Spectrin (green) and Aub (red), and DNA staining with DAPI (blue) show intact germline stem cells in tej48-5-tap125 mutants and heterozygous ovaries but cysts appeared to be arrested in mostly the two- to four-cell stage in tej48-5-tap125 double-mutant ovaries (bottom two panels). Scale bar = 5 μm. (C) Immunostaining for Bam (green), Aub (red) and DAPI (blue) shows a comparable Bam expression pattern between tej48-5-tap125 mutant and heterozygous controls. Scale bar = 5 μm. (D) Terminal deoxynucleotidyl transferase dUTP nick-end labeling staining shows dying germline cells in tej48-5-tap125 double-mutant germarium, but not in heterozygous control ovarioles or either single mutant. Scale bar = 5 μm.

Full size image

To study the maintenance of GSCs and their differentiation, we examined the fusomes and bag-of-marbles (bam) expression by immunostaining (Figure 2B,C and Additional file 1: Figure S2B; [32],[33]). We observed unbranched round fusomes in germline cells at the tip of female germaria and around the hub in testes in both control and double-mutant gonads that started losing germline cells, suggesting GSCs are maintained in double-mutant gonads. However, while 2-, 4-, 8- and 16-cell cysts were discernible by branched fusomes in the controls, most of the cysts in tej48-5-tap125 double mutants appear to be arrested at the two-cell stage, though some four- or eight-cell cysts were also observed (Figure 2B and Additional file 1: Figure S2B). Differentiation factor Bam expression pattern in double-mutant ovaries was similar to that in controls, suggesting no defects in differentiation (Figure 2C). To investigate the cause of loss of germline cells, we performed a terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) assay (Figure 2D and Additional file 1: Figure S2C). We observed apoptotic cells in the germarium and in the testis of the double mutants, while no TUNEL-positive germline cells were discernible in the control or either single-mutant germaria or the control testes. Approximately 50% (n =30) germaria had TUNEL-positive cells in two-dpe tej48-5-tap125 double-mutant ovaries: they start appearing in region 2 in germarium. The apoptosis in germline cells likely explains loss of germline cells in region 2b and late stage egg chambers attached to germarium of four- to seven-dpe tej48-5-tap125 flies (Figure 2A,B).

To examine any defect in the polarity determination, we stained ovaries with dorsal marker Gurken. While tap125-mutant oocytes showed normal anterior-dorsal Gurken localization as we previously observed in tej mutants, Gurken expression was not detectable in the tej48-5-tap125 double-mutant ovaries, indicating a severe defect in polarity establishment (Additional file 1: Figure S2D; [16]). Consistent with this observation, the eggs laid by the double-mutant females were also devoid of dorsal appendages (data not shown). Taken together, these results suggest that tap and tej are required together for proper germline survival, development and polarity formation in gonads.

tap is dispensable for fertility but is required for retroelement repression

Loss of function of many nuage components leads to derepression of retroelements in animal gonads (reviewed in [1],[2]). We examined whether tap also participates in retrotransposon repression by comparing expression levels of representative retroelements between tap125 mutants and heterozygous control ovaries with quantitative RT-PCR (qRT-PCR). The tap125-mutant ovaries exhibited a slight upregulation of TART, HeT-A and I-element, which are targeted by piRNAs in germline cells, but there was no significant effect on the expression of ZAM and Gypsy, which are regulated by piRNAs in gonadal somatic cells (Figure 3A). The tap125-mutant testes also displayed high expression of the Stellate (Ste) protein, which is repressed by su(ste) piRNA (Figure 3B; [4]). qRT-PCR also revealed significant upregulation of ste transcript in tap125-mutant testes compared to heterozygote controls (Figure 3C). These results suggest that tap function, although dispensable for fertility in Drosophila, is required for transposon repression in germline cells.

Figure 3
figure 3

tap is required for retroelement repression and likely functions with tej . (A) Quantitative RT-PCR (qRT-PCR) showing fold increase in expression of few representative retroelements in tej48-5, tap125 and tej48-5-tap125 mutant ovaries compared to respective heterozygous controls. The tap125-mutant displays milder upregulation of TART, I-element, roo and Het-A, whereas the tej48-5-tap125 double mutant exhibits much more severe upregulation of these retroelements compared with both tej48-5and tap125 single mutants. Error bars represent standard deviations. (B) tap-, tej- and the double-mutant testes stained for Ste (green) and DAPI (blue). Top and bottom panels show the apex and posterior regions, respectively. Asterisks mark the hub of the testis. Square brackets denote the distance from the hub to the point where Ste crystals start to appear. Scale bar = 20 μm. (C) qRT-PCR showing increase in ste transcript levels in the tap125-mutant testes compared to their respective heterozygote controls, and confirms more severe Ste crystal formation in tej48-5-tap125 double mutants. The error bars represent the standard deviation.

Full size image

The tej48-5-tap125 double-mutant females exhibited more severe derepression of reteroelements targeted by piRNAs in germline cells compared to either single mutant (Figure 3A; [10]). By contrast, expression levels of reteroelements, which are predominantly expressed in somatic cells, did not differ significantly in the double mutants compared with the heterozygous controls (Figure 3A). Similarly, expression of Ste protein and transcript in the male germline was higher in the double mutants than in either single mutant (Figure 3B,C). Ste crystals were longer and appeared earlier during gametogenesis in double mutants (square brackets in Figure 3B). These results suggest that tej and tap are functionally related for transposon repression in the Drosophila germline.

tap likely functions synergistically with tej for localization of piRNA pathway components in the germline

Many nuage and/or piRNA components genetically interact in Drosophila as well as in other systems such as mouse: they appear to be interdependent for their proper localization to the nuage [9],[16],[21],[24],[26],[34]-[38]. We examined whether tap function is also required for localizing other nuage components to the nuage and vice versa. Although all of the examined nuage components - Vas, Qin, Tej, Aub, Ago3, Krimp and Mael - localized to the perinuclear nuage, they often formed larger aggregates in tap125-mutant ovaries (Additional file 1: Figure S3A). In reciprocal experiments, in which we examined Tap localization in nuage component mutants, Tap remained unaffected and formed perinuclear foci in all the examined mutants (Additional file 1: Figure S3B). These results suggest that tap alone likely has a minor role in localization of examined nuage components. We previously showed that Vas, but not the other piRNA components such as Aub, Ago3, Krimp and Mael, depends on tej function [16]. By contrast, in the absence of both tej and tap function, Vas, as well as all examined piRNA pathway components, was displaced to cytoplasm from the perinuclear nuage (Additional file 1: Figure S3C).

Defects in localization of piRNA component proteins in tej48-5-tap125 ovaries indicates that tej and tap likely function together for their localization. To address the nature of this functional relation between tej and tap, we performed complementation analysis (Additional file 1: Figure S4). Tap expression either in tej48-5-tap125 double-mutant or in tej48-5 single-mutant germline cells failed to rescue the defects in perinuclear localization of Krimp, Aub and Ago3. However, Tej expression in double mutants brought them back to the perinuclear region, although they formed larger foci than the heterozygous controls, which was reminiscent of their localization in tap125 mutants (Additional file 1: Figure S3A). In summary, overexpression of either Tej or Tap in tej48-5-tap125 mutants manifests the observed phenotypes in the reciprocal single mutants, suggesting that Tej and Tap cannot complement each other's function and likely have a synergistic relationship for localization of piRNA pathway components.

tej and tap together are required for nuclear localization of Piwi in germline cells

The other distinct defect occurring in the tej48-5-tap125 double mutant but not in either the tej48-5 or tap125 mutants was the cytoplasmic localization of Piwi in germline cells, whereas in the heterozygous controls Piwi localized to the nucleus (Figure 4A and Additional file 1: Figure S5A). In the gonadal somatic cells, however, Piwi remained localized to the nucleus in the double mutants, like those in the heterozygous controls. The Piwi expression levels in tej48-5-tap125, tej48-5 and tap125 mutants were found to be comparable to those in respective heterozygotes by western blot analysis (Figure 4B), suggesting that loss of tej-tap function together leads to Piwi mis-localization without affecting its expression level. Furthermore, Myc-Piwi expressed from a native promoter in addition to endogenous Piwi in tej48-5-tap125 double-mutant germline cells remained in the cytoplasm, whereas it localized to the nucleus in the somatic follicle cells (Figure 4C and Additional file 1: Figure S5B), suggesting that simultaneous impairment of tej and tap functions prevents Piwi from entering the nucleus in germline cells. In addition, the localization pattern of another primary piRNA pathway component, Armitage, in the double-mutant gonadal somatic cells remained comparable to that in control (Additional file 1: Figure S5C; [39]). These results suggest that loss of tej and tap together does not affect the localization of piRNA pathway components in gonadal somatic cells.

Figure 4
figure 4

Piwi fails to localize to the nucleus in germline cells of the tej-tap double mutant. (A) Ovaries stained for Piwi (green) and DAPI (blue). Piwi localized to the nucleus in the somatic cells but failed to localize to the nucleus of germline cells of the tej48-5-tap125 double mutants. (B) Western blotting with anti-Piwi antibody showing no significant difference in Piwi expression levels in tej48-5-, tap125- and tej48-5-tap125-mutant ovaries in comparison to their respective heterozygous controls. The same blot was re-probed with anti-α-Tubulin to examine loading. (C) Expression of Myc-Piwi in tej48-5-tap125 ovaries does not rescue nuclear localization of Piwi in germline cells. Immunostaining shows cytoplasmic Myc-Piwi in germline cells of tej48-5-tap125 double-mutant ovaries. Scale bar = 5 μm.

Full size image

Tap physically interacts with piRNA pathway components

Tej was previously shown to physically interact with some of the piRNA pathway proteins such as Vas, Spn-E and Aub [16]. To examine if Tap also physically interacts with some piRNA pathway components, immunoprecipitated Tap from ovarian lysate with the anti-Tap antibody was examined for interaction with some piRNA pathway components (Figure 5A). Indeed, Spn-E, Aub and Tej were pulled down along with Tap, suggesting that Tap interacts with those in the germline. However, we detected a very small amount of Ago3 in Tap immunoprecipitate, suggesting a weak interaction between Tap and Ago3. We also observed Tap and Vas interaction in a reciprocal manner where we detected Tap in anti-Vas immunoprecipitate.

Figure 5
figure 5

Tap physically interacts with other components of the ping-pong amplification pathway. (A) Immunoprecipitation with anti-Tap antibody using ovarian lysates followed by western blotting. Vas, Aub, Spn-E, Tej and a trace amount of Ago3 (arrowhead) were pulled down along with Tap. (B-E) S2 cells were co-transfected with FLAG an octa-peptide (DYKDDDDK)-Tap along with V5-Vas, Myc-Spn-E, Myc-Aub, Myc-Ago3, FLAG-Tej and Myc-Tap, and the cell lysates were subjected to immunoprecipitation with anti-FLAG antibodies. IgG was used as control in all IP experiments. (B,C) V5-Vas and Myc-Spn-E were pulled down with FLAG-Tap but not with IgG. (D) Both Aub and Ago3 were pulled down with FLAG-Tap but not with the control IgG. (E) FLAG-Tap was pulled down and blotted with FLAG or Myc antibody. A small amount of Tap precipitated with Tej as well as with itself. Similarly, Myc-Tej was also pulled down with FLAG-Tej. IgG: immunoglobulin G, IP: immunoprecipitation, WB: western blotting.

Full size image

We further confirmed these interactions in S2 cells; FLAG (DYKDDDK)-tagged Tap was transfected separately with V5-tagged Vas, Myc-tagged Spn-E, Myc-tagged Aub, or Myc-tagged Ago3 (Figure 5B-D). We pulled down FLAG-Tap and detected tagged Vas, Aub, Ago3 and Spn-E in immunoprecipitate, suggesting that Tap interacts with them in the absence of any other germline factors. To confirm interaction between Tej and Tap, we co-transfected Myc- and FLAG- tagged Tap and Tej in S2 cells and performed immunoprecipitation (IP). Tap and Tej co-immunoprecipitated with each other in reciprocal IP experiments, suggesting that they interact in the absence of any other germline proteins (Figure 5E). Taken together, our IP experiments suggest that Tap can interact not only with its paralog, Tej, but also with other piRNA pathway components. The observed physical interaction of Tap with Tej and other piRNA pathway components supports our earlier observation of functional relationships between Tap and Tej for germline development, piRNA production and transposon repression.

The tap-, tej- and tap-tej mutants display defects in piRNA production in germline

Next, to understand the roles of tap and tej in piRNA biogenesis, we performed deep sequencing of small RNAs isolated from tej48-5, tap125, tej48-5-tap125 and their respective heterozygous ovaries. The small RNA libraries were aligned to the genome and canonical transposons, and then normalized with small nucleolar RNA-derived small RNAs, genic-endo-siRNAs and non-coding RNAs with respective heterozygous controls (Additional file 2: Table S1). We examined small RNAs, from 23 to 29 nucleotides in size, for subsequent piRNA analysis, and considered antisense piRNAs to compare transposon-mapping piRNA levels between mutants and controls. The tap125-mutant ovaries only had a 16% reduction in the number of genome-matching unique reads compared with the heterozygous control (Figure 6A). tap125 mutants did not show any significant decrease in the overall cluster-mapping piRNAs, including those mapping to the largest bidirectional cluster at 42AB. However, some other bidirectional clusters, such as those at 20B3, 62A, 80E, 3LHet and 3RHet in tap125 mutants, had a significant reduction in piRNAs (25% to 50%) (Figure 6B; Additional file 3: Table S2). These clusters housed several transposable elements (TEs) including TART-A, I-element, Het-A and roo, which showed slight depression in tap125-mutant ovaries (Figure 3A), suggesting that the reduction in piRNAs may have caused the observed derepression.

Figure 6
figure 6

The tap gene is required for robust piRNA production against germline transposable elements, while tap along with tej is required to maintain piRNA population in germline. (A) Abundance of genome-matching unique reads, 21 to 29 nucleotides in length, in tap125-, tej48-5- and tej48-5-tap125-mutant ovaries and their respective heterozygous controls. The tap mutants showed reduced numbers of 23- to 29-nucloetide small RNAs, but the tej48-5-tap125 double mutants showed the most severe reduction in comparison to both single mutants. (B) Mapping of the 23- to 29-nucloetide sequences to bidirectional piRNA clusters at 20B3 and 42AB, and a single-strand piRNA cluster, flamenco. A feeble reduction in bidirectional cluster mapping piRNAs in tap125 mutants was discernible compared to tej48-5 mutants, while tej48-5-tap125 double mutants had a greater reduction than both single mutants.

Full size image

The overall transposon-mapping piRNAs were also not significantly reduced in the tap mutants. However, we observed up to 57% reduction in the piRNAs mapping to a subset of transposons known to be repressed by piRNAs in germline, such as doc, Rt1b, TART-B, I-element and roo, in comparison to heterozygous controls (Wilcoxon t-test; Z-score -2.45, P = 0.01; Figure 7A; Additional file 4: Table S3; [10]). We also observed a 10% to 49% reduction in ping-pong piRNAs mapping to these transposons in tap mutants (Figure 7B). By contrast, tap125 mutation did not lead to any statistically significant decrease in the piRNAs mapping to transposons targeted by piRNAs in both germline and somatic cells and those predominantly in in somatic cells. This indicates that tap is likely required for production of piRNAs for a subset of transposons in germline cells.

Figure 7
figure 7

tej and tap likely function together for production of cluster-derived and ping-pong piRNAs. (A) Bar plots showing reduction separately for piRNAs mapping to transposons families expressed predominantly in germline, both germline and soma, and predominantly in soma. The tej48-5-tap125 mutants showed a more severe reduction in piRNAs targeting transposons expressed in germline and both germline and soma compared to that in both single mutants. (B) Heat maps representing the ratio of ping-pong piRNAs (10-nucleotide overlap) to piRNA pairs with overlaps of 2 to 26 nucleotides mapping to transposable elements (TEs) of three different subsets: those predominantly expressed in the germline (top panel), in both the germline and soma (middle panel), and predominantly in somatic cells (bottom panel). tap125 mutants had a less severe reduction in the ping-pong piRNAs mapping to TEs predominantly repressed in germline than the tej48-5-tap125 mutants, which suffered the most severe loss in ping-pong ratios compared to both single mutants.

Full size image

Though the loss of tap homologue, tej, itself led to a significant decrease in the overall piRNA levels, tej48-5-tap125 double mutants exhibited further reduction in piRNAs (Figures 6 and 7), suggesting that tap also functions with tej for piRNA production. The overall genome-mapping piRNAs were more severely reduced in the tej48-5-tap125 double mutants (64%) than in the tej48-5 mutants (53%) (Figure 6A). Similarly, loss of both tej and tap led to a greater reduction in cluster mapping piRNAs (82% reduction in comparison to the heterozygous control) than tej mutant alone (74% reduction in comparison to heterozygous control; Additional file 1: Figure S6A, Additional file 3: Table S2). The tej48-5-tap125 double-mutant ovaries had fewer piRNAs mapping to all bidirectional clusters, including that at 42AB, compared to single mutants (Figure 6B and Additional file 3: Table S2). The double mutant also showed a greater reduction in the proportion of cluster mapping reads with U at the first position compared with both single mutants (Additional file 1: Figure S6A,B). These results suggest that loss of tej and tap together causes a more severe reduction in cluster-derived piRNA production in germline cells. We did not observe a significant reduction in piRNAs derived from flamenco or other major unidirectional clusters in single or double mutants (Figure 7A and Additional file 3: Table S2), further supporting a germline-specific function of tej and tap in piRNA production. The slight decrease (10%) in flamenco-mapping piRNAs in the double mutants could be a secondary effect resulting from the distortion of ovarian structure in the tej48-5-tap125 mutants.

The tej48-5-tap125 mutants also showed a more severe reduction in overall transposon-mapping piRNAs (73% overall and 81% in antisense piRNAs), compared with tej mutants (62% overall and 70% in antisense) (Additional file 1: Figure S6C,D; Additional file 4: Table S3). The piRNAs of 26 to 29 nucleotides in length were more severely reduced in the tej48-5-tap125 mutants than in the tej48-5 mutants (Additional file 1: Figure S6D).

The piRNAs mapping to transposons predominantly targeted in germline were more severely reduced in the tej48-5-tap125 mutants (88%, Z-score: −3.98, P = 0.00006,) than the tej mutants (80%, Z-score: −3.8, P = 0.0001; Figure 7A, left panel). Similarly, only the tej48-5-tap125 double-mutant ovaries had a significant reduction in piRNAs mapping to the transposons targeted by both germline and somatic piRNAs (29%, Z-score −1.88, P = 0.008) while no significant change in these piRNAs was observed in tej48-5 mutants (10%, Z-score: 0.746, P = 0.445; Figure 7A, middle panel). However, no significant loss in piRNAs targeting transposons predominantly expressed in somatic cells was observed in tej48-5-tap125 double mutants or tej48-5 mutants (Figure 7A, right panel). Notably, in tej single mutants, piRNAs mapping to blood, HMS-Beagle and rover were increased compared with the heterozygous control (Additional file 4: Table S3); while the antisense piRNAs matching to these transposons were reduced, sense piRNAs were largely increased. However, no such increase in sense piRNAs was observed in tej48-5-tap125 double mutants (Additional file 5: Table S4).

The double mutants also had an overall higher reduction in the transposon-mapping sense piRNAs with A at 10th position and antisense piRNAs with U at 1st position (Additional file 1: Figure S6E), indicating a defect in the secondary processing. To analyze this, we calculated the ratio of sense-antisense piRNA pairs with a 10-nucleotide overlap to piRNA pairs with any overlap in length. The tej48-5-tap125 double mutants showed a more severe decrease in the above ratios for transposons expressed in the germline and in both germline and soma than the tej single mutants. This was also supported by greater loss in the ping-pong piRNA pairs in double mutants than in the tej mutants (96% versus 90%, compared with those in each heterozygous control, respectively; Additional file 1: Figure S6E). These observations are consistent with a greater derepression of transposons in tej48-5-tap125 double mutants than that in tej single-mutant ovaries (Figure 3). More severe loss in ping-pong piRNAs in double mutants also emphasizes the requirement of tej and tap together for secondary piRNA production, and supports the observed synergistic relationship between them for piRNA production.

Discussion

In this study we have characterized Tap, the paralog of Tej, which was previously reported as an essential piRNA pathway component that localizes to the nuage [16]. Like Tej, Tap is expressed predominantly in germline cells. tap genetically and physically interacts with Piwi family proteins and other piRNA pathway components. A reduction in germline piRNAs and upregulation of TE and ste expressions confirm participation of tap in piRNA pathways. Similarly, mouse ortholog of Tap, Tdrd7, was reported to be involved in the suppression of the retrotransposon LINE1 and localizes to chromatoid bodies, which is the equivalent structure of the Drosophila nuage [17],[21]. In Tdrd7-knockout mouse testes, however, piRNA production is not affected, but LINE1 appears to be translationally upregulated [21]. This could be because Tdrd5 may have a more robust role in piRNA production in vertebrates than that in Drosophila, and the loss of Tdrd7 may be fully compensated for by Tdrd5. Analysis of piRNAs in Tdrd5 and Tdrd7 double-knockout mouse would shed light on their potential synergistic function in vertebrate. In addition, unlike Tap, mouse Tdrd7 is also expressed in somatic tissue - lens fiber cells - and its loss of function results in defects in spermatogenesis and somatic phenotypes such as cataract and glaucoma in mouse and human [21],[40]. This suggests that, while mammalian Tdrd7 has a wider role in gonads and somatic tissues, Tap may have a specific role in Drosophila gonads. However, we cannot eliminate the possibility that tap is expressed at a very low level in somatic tissues and that its function is dispensable in the laboratory environment.

The absence of robust phenotypes in tap125 mutants questions the importance of tap. By contrast, loss of function of its paralog tej causes severe reduction in piRNAs in germline and mis-localization of several piRNA proteins from the nuage (Figures 6 and 7; Additional file 1: Figure S3; [16]). Our study with the tej48-5-tap125 mutants underscored the importance of the synergistic function of tap and tej. Loss of tej and tap together leads to the loss of germline cells by apoptosis in the germarium (Figure 2D), indicating that they function together to maintain early germline cells. In late stages, tej and tap together are required for polarity formation, which is indicated by loss of Gurken expression (Additional file 1: Figure S2D). In addition, we observed mis-localization of all examined nuage components and a statistically more robust reduction in cluster- and transposon-mapping piRNAs in double mutants (Figures 6 and 7; Additional file 3: Table S2 and Additional file 4: Table S3). These results also indicate that Tej and Tap function together for the piRNA pathway, and explain the higher derepression of TEs in double mutants than in tej mutants. The reduction in the ratio of antisense piRNAs having U at the first position and in ping-pong-derived piRNAs was also more severe in double mutants than in either single mutant. These defects suggest that Tej and Tap together could support primary processing, probably by engaging Aub and/or Piwi, and a more robust ping-pong amplification cycle for piRNA amplification.

A synergistic relationship between tej and tap for piRNA production is also suggested by the mis-localization of Piwi from the nucleus in germline cells of double mutants, while Piwi stayed in the nucleus of germline cells in both single mutants (Figure 4 and Additional file 1: Figure S5A). A recent study showed that the ablation of piRNA binding ability of Piwi leads to its retention in the cytoplasm of germline cells [41]. Hence, it may also be possible that Tej and Tap together are required for the piRNA loading onto Piwi in the germline cells of Drosophila. Overexpression of either tej or tap in the double mutant did not fully rescue the phenotype of the double mutants (Additional file 1: Figure S4), suggesting that they are not functionally redundant, but act synergistically for piRNA pathway and germline development. Similarly, Tdrd7 and Tdrd6 double-knockout mice exhibited more severe defects in chromatoid body and Miwi localization than single mutants [21],[42], suggesting a conservation of functional relationship among piRNA components across species. However, it is currently unclear whether the more severe defects in germline development in the double mutants are correlated with heavy loss of piRNAs or if tej and tap have any piRNA-independent role in germline development.

Conclusions

We here report on tap, a paralog of a germline piRNA pathway protein tej. Although the tap functions in the piRNA pathway, a milder derepression of transposons and milder decrease in piRNAs indicate it probably does not have a robust role in the piRNA pathway. However, tap likely functions together with tej for maintenance of germline cells in early stages and proper development of the germline, which is reflected by apoptosis in germline cells, atrophic ovaries, and loss of Gurken expression in double-mutant ovaries. We also showed that tej and tap function in a synergistic manner in a complex for piRNA production to safeguard the germline genome from transposons. Our findings describe a functional relationship between two germline piRNA pathway components. We believe that studies on functional relationships between piRNA pathway components might prove helpful in elucidating the mechanistic understanding of the piRNA pathway.

Methods

Drosophila strains

Either y w or the respective heterozygote was used as a control. A loss-of function allele of tap, tap125 was isolated from more than 150 independent excision lines of a P-element insertion line, P{EPgy2}G8920[EY02725]/CyO, by PCR-based screening using the primers Tap 1Fw (AGCCTTTTACTCCTTTGGAACC) and Tap 2 Rv (CGACTTCCTTCGTTATTTGACC). The tap125 allele lost approximately 1.33 kb in the locus and instead contained a 28-nucleotide insertion, which is possibly a remnant of the P-element. The mutant alleles and allelic combinations used in the study were tap125, tap125/Df(2R)BSC19, tej48-5[16], UASp-Venus-Tej (in this study), UASp-Myc-Tap (in this study), qinM41–13 (previously designated kumoM41–13; [26]), maelM391/Df(3 L)79E-F[43],[44], vasPH165[45], spn-E616/hls3987[46],[47], aubNH2/N11[48],[49], ago3t2/t3[9], krimpf06583[24], piwi1[50], Myc-Piwi [51] and the tap protein trap line CC00825[31]. The tej48-5-tap125double mutant was generated by recombination and was screened by a PCR-based method.

The full-length Tap coding sequence was amplified by PCR with the primers CACC-ATGGAAAAGCAGGAGGTC and TGTTGCTGGCTGTGCGTGCTT, using the cDNA generated from ovarian RNA and cloned into pENTRâ„¢/D-TOPO (Invitrogen, life technologies Grand Island, NY, USA) in accordance with the manufacturer's protocol. The resulting pENTR Tap and previously generated pENTR Tej were recombined into pPMW and pPVW, respectively [16]. The pPMW-Tap and pPVW-Tej plasmids were injected into y w embryos to generate transgenic flies using a standard protocol [52]. The expression of transgenes was driven in the germline by nosGal4VP16[53].

Antibody generation

Rat anti-Tap antiserum was generated against a portion of His-tagged Tap (amino acids 26 to 159). The corresponding fragment was amplified with the primers Tap antigen Fw (CACC-ACGCTGCGGTCCATCGTC) and Tap Antigen Rv (TTA-GCCCGTTAGATCTTGTTT). After cloning into pENTRâ„¢/D-TOPO, this sequence was recombined into pDEST17 (Invitrogen) according to the manufacturer's instructions. The His-tagged peptide was purified and injected into rats with complete or incomplete adjuvant (Thermo Scientific/Pierce, Thermo Scientific, Waltham, MA USA).

Immunostaining

Ovaries were immunostained as described previously [24]. The antibodies used for immunostaining were rat polyclonal anti-Tap (1:1,000), rabbit polyclonal anti-Tej (1:250) [16], guinea pig polyclonal anti-Vas (1:1,000) [16], mouse anti-Aub (1:1,000) [7], mouse anti-Ago3 (1:1,000) [54], rabbit anti-Krimp (1;10,000) [24], guinea pig anti-Mael (1:500) [55], mouse anti-Gurken 1D12 (1:10) (Hybridoma Bank, Iowa City, IA, USA), rabbit anti-Qin (1:1,000) [26], mouse anti-Piwi (1:1) (from Dr Siomi), rabbit anti-Armitage (1:1,000) [56], guinea pig anti-Rhino (1:1,000) [57], mouse anti-Myc (1:1,000) (Sigma, St. Louis, MO, USA), rabbit anti-Ste (1:1,000) [58], rabbit anti-α spectrin (1:2,500) [59] and guinea pig anti-Bam-C (1:200, from Dr McKearin). Secondary antibodies were Alexa Fluor 488-, 555-, 633-conjugated goat anti-rabbit, anti-mouse, anti-rat and anti-guinea pig IgG (1:400) (Molecular Probes, Eugene, Oregon, USA). Images were acquired with a Carl Zeiss Exciter confocal microscope, Oberkochen, Germany and processed in Adobe Photoshop.

TUNEL assay

The TUNEL assay was performed using an ApopTag® Fluorescein In Situ Apoptosis Detection Kit (Millipore, Billerica, Massachusetts, USA) in accordance with the manufacturer's protocol.

Western blot analysis and immunoprecipitation

Ovaries were dissected in Grace’s medium and processed for IP as described previously [16]. For western blotting, one-half ovary equivalent lysate was loaded into each lane of an 8% or 10% SDS-PAGE. The following primary antibodies were used: mouse anti-Aub (1:1,000, from Dr Siomi), mouse anti-Ago3 (1:500, from Dr Siomi), rat anti-Tap (1:1,000, this study), mouse anti-c-Myc 9E10 (1:5000, Sigma), mouse anti-HA (1:5,000, Roche, BASEL, Switzerland), mouse anti-FLAG M2 and its horseradish peroxidase (HRP)-conjugated secondary antibody (1:1,000, Sigma), guinea pig anti-Vas (1:5,000) [16], rabbit anti-Piwi (1:500, Abcam, Cambridge, England, United Kingdom Ab5207), mouse anti-Piwi (1:50, from Dr Siomi), rabbit anti-SpnE (1:500, from Dr Dahua Chen) and mouse anti-α-Tubulin DM1A (1:1,000, Santa Cruz Biotechnology, Santa Cruz Biotechnology, Dallas, Texas, U.S.A.). Immunoreactive bands were visualized using HRP-conjugated goat anti-guinea pig (Dako, Dako North America, Inc. Carpinteria, CA, USA), anti-rabbit, anti-rat or anti-mouse secondary antibodies (Bio-Rad, Hercules, CA, United States of America) at 1:5,000, and developed with the SuperSignal West Pico Chemiluminescent Substrate detection reagent (Thermo Scientific).

S2 cell experiments

pENTRâ„¢/D-TOPO containing Tap, Tej or Ago3 was recombined into either pAFW or pAMW (The Drosophila Gateway Vector Collection, Carnegie Institution for Science Baltimore, Maryland, USA) following manufacturer's protocol. Vas-V5, FLAG-Tej and Myc-SpnE generation were described previously [16]. Transfections and IPs with S2 cells lysates were performed as described previously [16].

Real-time RT-PCR

Total RNA was extracted from ovaries or testes with TRIzol (Invitrogen) according to the manufacturer's protocol. Real-time RT-PCR was performed as described previously [24]. The primer sequences for HetA, TART, I-element, actin5C, roo and ZAM were described in [24].

Small RNA sequencing and analysis

RNAs were extracted from hand-dissected ovaries of tej48-5, tap125 and tej48–5- tap125, and their corresponding heterozygotes. Small RNAs ranging from 18 to 30 nucleotides were isolated by PAGE fractionation and were used for library generation for deep sequencing. Deep sequencing was performed on HiSeq2000 at Macrogen Inc. (Seoul, Korea). All six libraries were normalized with noncoding RNAs derived from snoRNAs [60], endogenous siRNAs [10] and noncoding RNAs (Additional file 2: Table S1). The libraries were mapped to Drosophila genome (Rel 5, excluding Uextra) without any mismatches. To analyze piRNA matching to clusters, only 23- to 29-nucleotide reads that uniquely mapped to the genome were considered (cluster information was taken from Brennecke et al. [6]). The piRNAs mapping to the clusters were counted in 10-nucleotide windows for plotting. The libraries were mapped to transposons allowing two mismatches. To analyze ping-pong generated piRNAs, we calculated sense-antisense piRNA pairs having an overlap between 2 and 26 nucleotides using in-house programs. The ping-pong ratios were calculated by dividing the numbers of reads containing a 10-nucleotide overlap with the sum of reads containing any overlap between 2 and 26 nucleotides.

Availability of supporting data

The small RNA deep-sequencing libraries without 30-nucleotide rRNA reads from the single and double mutants and their corresponding heterozygotes were deposited in the National Center for Biotechnology under the accession number [SRP044384]. The untrimmed raw fastq files are available upon request.

Additional files

Abbreviations

dpe:

days post eclosion

GFP:

green fluorescent protein

GSC:

germline stem cells

HRP:

horseradish peroxidase

IgG:

immunoglobulin G

IP:

immunoprecipitation

kDA:

kiloDaltons

piRNA:

Piwi-interacting RNA

RT-PCR:

reverse transcription polymerase chain reaction

siRNA:

small interfering RNA

TE:

transposable elements

TUNEL:

terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling

References

  1. Siomi MC, Sato K, Pezic D, Aravin AA: PIWI-interacting small RNAs: the vanguard of genome defence. Nat Rev Mol Cell Biol. 2011, 12: 246-258. 10.1038/nrm3089.

    Article  CAS  PubMed  Google Scholar 

  2. Pek JW, Patil VS, Kai T: piRNA pathway and the potential processing site, the nuage, in the Drosophila germline. Dev Growth Differ. 2012, 54: 66-77. 10.1111/j.1440-169X.2011.01316.x.

    Article  CAS  PubMed  Google Scholar 

  3. Saito K, Nishida KM, Mori T, Kawamura Y, Miyoshi K, Nagami T, Siomi H, Siomi MC: Specific association of Piwi with rasiRNAs derived from retrotransposon and heterochromatic regions in the Drosophila genome. Genes Dev. 2006, 20: 2214-2222. 10.1101/gad.1454806.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  4. Vagin VV, Sigova A, Li C, Seitz H, Gvozdev V, Zamore PD: A distinct small RNA pathway silences selfish genetic elements in the germline. Science. 2006, 313: 320-324. 10.1126/science.1129333.

    Article  CAS  PubMed  Google Scholar 

  5. Aravin AA, Hannon GJ, Brennecke J: The Piwi-piRNA pathway provides an adaptive defense in the transposon arms race. Science. 2007, 318: 761-764. 10.1126/science.1146484.

    Article  CAS  PubMed  Google Scholar 

  6. Brennecke J, Aravin AA, Stark A, Dus M, Kellis M, Sachidanandam R, Hannon GJ: Discrete small RNA-generating loci as master regulators of transposon activity in Drosophila. Cell. 2007, 128: 1089-1103. 10.1016/j.cell.2007.01.043.

    Article  CAS  PubMed  Google Scholar 

  7. Gunawardane LS, Saito K, Nishida KM, Miyoshi K, Kawamura Y, Nagami T, Siomi H, Siomi MC: A slicer-mediated mechanism for repeat-associated siRNA 5' end formation in Drosophila. Science. 2007, 315: 1587-1590. 10.1126/science.1140494.

    Article  CAS  PubMed  Google Scholar 

  8. Houwing S, Kamminga LM, Berezikov E, Cronembold D, Girard A, van den Elst H, Filippov DV, Blaser H, Raz E, Moens CB, Plasterk RH, Hannon GJ, Draper BW, Ketting RF: A role for Piwi and piRNAs in germ cell maintenance and transposon silencing in Zebrafish. Cell. 2007, 129: 69-82. 10.1016/j.cell.2007.03.026.

    Article  CAS  PubMed  Google Scholar 

  9. Li C, Vagin VV, Lee S, Xu J, Ma S, Xi H, Seitz H, Horwich MD, Syrzycka M, Honda BM, Kittler EL, Zapp ML, Klattenhoff C, Schulz N, Theurkauf WE, Weng Z, Zamore PD: Collapse of germline piRNAs in the absence of Argonaute3 reveals somatic piRNAs in flies. Cell. 2009, 137: 509-521. 10.1016/j.cell.2009.04.027.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  10. Malone CD, Brennecke J, Dus M, Stark A, McCombie WR, Sachidanandam R, Hannon GJ: Specialized piRNA pathways act in germline and somatic tissues of the Drosophila ovary. Cell. 2009, 137: 522-535. 10.1016/j.cell.2009.03.040.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  11. Eddy EM: Germ plasm and the differentiation of the germ cell line. Int Rev Cytol. 1975, 43: 229-280. 10.1016/S0074-7696(08)60070-4.

    Article  CAS  PubMed  Google Scholar 

  12. Juliano C, Wang J, Lin H: Uniting germline and stem cells: the function of Piwi proteins and the piRNA pathway in diverse organisms. Annu Rev Genet. 2011, 45: 447-469. 10.1146/annurev-genet-110410-132541.

    Article  CAS  PubMed  Google Scholar 

  13. Kirino Y, Kim N, de Planell-Saguer M, Khandros E, Chiorean S, Klein PS, Rigoutsos I, Jongens TA, Mourelatos Z: Arginine methylation of Piwi proteins catalysed by dPRMT5 is required for Ago3 and Aub stability. Nat Cell Biol. 2009, 11: 652-658. 10.1038/ncb1872.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  14. Siomi MC, Mannen T, Siomi H: How does the royal family of Tudor rule the PIWI-interacting RNA pathway?. Genes Dev. 2010, 24: 636-646. 10.1101/gad.1899210.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  15. Nishida KM, Okada TN, Kawamura T, Mituyama T, Kawamura Y, Inagaki S, Huang H, Chen D, Kodama T, Siomi H, Siomi MC: Functional involvement of Tudor and dPRMT5 in the piRNA processing pathway in Drosophila germlines. EMBO J. 2009, 28: 3820-3831. 10.1038/emboj.2009.365.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  16. Patil VS, Kai T: Repression of retroelements in Drosophila germline via piRNA pathway by the Tudor domain protein Tejas. Curr Biol. 2010, 20: 724. 30-10.1016/j.cub.2010.02.046.

    Article  PubMed  Google Scholar 

  17. Hosokawa M, Shoji M, Kitamura K, Tanaka T, Noce T, Chuma S, Nakatsuji N: Tudor-related proteins TDRD1/MTR-1, TDRD6 and TDRD7/TRAP: domain composition, intracellular localization, and function in male germ cells in mice. Dev Biol. 2007, 301: 38-52. 10.1016/j.ydbio.2006.10.046.

    Article  CAS  PubMed  Google Scholar 

  18. Strasser MJ, Mackenzie NC, Dumstrei K, Nakkrasae LI, Stebler J, Raz E: Control over the morphology and segregation of Zebrafish germ cell granules during embryonic development. BMC Dev Biol. 2008, 8: 58-10.1186/1471-213X-8-58.

    Article  PubMed Central  PubMed  Google Scholar 

  19. Smith JM, Bowles J, Wilson M, Teasdale RD, Koopman P: Expression of the Tudor-related gene Tdrd5 during development of the male germline in mice. Gene Expr Patterns. 2004, 4: 701-705. 10.1016/j.modgep.2004.04.002.

    Article  CAS  PubMed  Google Scholar 

  20. Vagin VV, Wohlschlegel J, Qu J, Jonsson Z, Huang X, Chuma S, Girard A, Sachidanandam R, Hannon GJ, Aravin AA: Proteomic analysis of murine Piwi proteins reveals a role for arginine methylation in specifying interaction with Tudor family members. Genes Dev. 2009, 23: 1749-1762. 10.1101/gad.1814809.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  21. Tanaka T, Hosokawa M, Vagin VV, Reuter M, Hayashi E, Mochizuki AL, Kitamura K, Yamanaka H, Kondoh G, Okawa K, Kuramochi-Miyagawa S, Nakano T, Sachidanandam R, Hannon GJ, Pillai RS, Nakatsuji N, Chuma S: Tudor domain containing 7 (Tdrd7) is essential for dynamic ribonucleoprotein (RNP) remodeling of chromatoid bodies during spermatogenesis. Proc Natl Acad Sci U S A. 2011, 108: 10579-10584. 10.1073/pnas.1015447108.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  22. Anantharaman V, Zhang D, Aravind L: OST-HTH: a novel predicted RNA-binding domain. Biol Direct. 2010, 5: 13-10.1186/1745-6150-5-13.

    Article  PubMed Central  PubMed  Google Scholar 

  23. Callebaut I, Mornon JP: LOTUS, a new domain associated with small RNA pathways in the germline. Bioinformatics. 2010, 26: 1140-1144. 10.1093/bioinformatics/btq122.

    Article  CAS  PubMed  Google Scholar 

  24. Lim AK, Kai T: Unique germ-line organelle, nuage, functions to repress selfish genetic elements in Drosophila melanogaster. Proc Natl Acad Sci U S A. 2007, 104: 6714-6719. 10.1073/pnas.0701920104.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  25. Liu L, Qi H, Wang J, Lin H: PAPI, a novel TUDOR-domain protein, complexes with AGO3, ME31B and TRAL in the nuage to silence transposition. Development. 2011, 138: 1863-1873. 10.1242/dev.059287.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  26. Anand A, Kai T: The Tudor domain protein Kumo is required to assemble the nuage and to generate germline piRNAs in Drosophila. EMBO J. 2012, 31: 870-882. 10.1038/emboj.2011.449.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  27. Zhang Z, Xu J, Koppetsch BS, Wang J, Tipping C, Ma S, Weng Z, Theurkauf WE, Zamore PD: Heterotypic piRNA Ping-Pong requires qin, a protein with both E3 ligase and Tudor domains. Mol Cell. 2011, 44: 572-584. 10.1016/j.molcel.2011.10.011.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  28. Liang L, Diehl-Jones W, Lasko P: Localization of vasa protein to the Drosophila pole plasm is independent of its RNA-binding and helicase activities. Development. 1994, 120: 1201-1211.

    CAS  PubMed  Google Scholar 

  29. Hay B, Ackerman L, Barbel S, Jan LY, Jan YN: Identification of a component of Drosophila polar granules. Development. 1988, 103: 625-640.

    CAS  PubMed  Google Scholar 

  30. Lasko PF, Ashburner M: Posterior localization of Vasa protein correlates with, but is not sufficient for, pole cell development. Genes Dev. 1990, 4: 905-921. 10.1101/gad.4.6.905.

    Article  CAS  PubMed  Google Scholar 

  31. Buszczak M, Paterno S, Lighthouse D, Bachman J, Planck J, Owen S, Skora AD, Nystul TG, Ohlstein B, Allen A, Wilhelm JE, Murphy TD, Levis RW, Matunis E, Srivali N, Hoskins RA, Spradling AC: The Carnegie protein trap library: a versatile tool for Drosophila developmental studies. Genetics. 2007, 175: 1505-1531. 10.1534/genetics.106.065961.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  32. McKearin DM, Spradling AC: bag-of-marbles: a Drosophila gene required to initiate both male and female gametogenesis. Genes Dev. 1990, 4: 2242-2251. 10.1101/gad.4.12b.2242.

    Article  CAS  PubMed  Google Scholar 

  33. de Cuevas M, Spradling AC: Morphogenesis of the Drosophila fusome and its implications for oocyte specification. Development. 1998, 125: 2781-2789.

    CAS  PubMed  Google Scholar 

  34. Chuma S, Hosokawa M, Kitamura K, Kasai S, Fujioka M, Hiyoshi M, Takamune K, Noce T, Nakatsuji N: Tdrd1/Mtr-1, a Tudor-related gene, is essential for male germ-cell differentiation and nuage/germinal granule formation in mice. Proc Natl Acad Sci U S A. 2006, 103: 15894-15899. 10.1073/pnas.0601878103.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  35. Reuter M, Chuma S, Tanaka T, Franz T, Stark A, Pillai RS: Loss of the Mili-interacting Tudor domain-containing protein-1 activates transposons and alters the Mili-associated small RNA profile. Nat Struct Mol Biol. 2009, 16: 639-646. 10.1038/nsmb.1615.

    Article  CAS  PubMed  Google Scholar 

  36. Shoji M, Tanaka T, Hosokawa M, Reuter M, Stark A, Kato Y, Kondoh G, Okawa K, Chujo T, Suzuki T, Hata K, Martin SL, Noce T, Kuramochi-Miyagawa S, Nakano T, Sasaki H, Pillai RS, Nakatsuji N, Chuma S: The TDRD9-MIWI2 complex is essential for piRNA-mediated retrotransposon silencing in the mouse male germline. Dev Cell. 2009, 17: 775-787. 10.1016/j.devcel.2009.10.012.

    Article  CAS  PubMed  Google Scholar 

  37. Wang J, Saxe JP, Tanaka T, Chuma S, Lin H: Mili interacts with Tudor domain-containing protein 1 in regulating spermatogenesis. Curr Biol. 2009, 19: 640-644. 10.1016/j.cub.2009.02.061.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  38. Yabuta Y, Ohta H, Abe T, Kurimoto K, Chuma S, Saitou M: TDRD5 is required for retrotransposon silencing, chromatoid body assembly, and spermiogenesis in mice. J Cell Biol. 2011, 192: 781-795. 10.1083/jcb.201009043.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  39. Olivieri D, Sykora MM, Sachidanandam R, Mechtler K, Brennecke J: An in vivo RNAi assay identifies major genetic and cellular requirements for primary piRNA biogenesis in Drosophila. EMBO J. 2010, 29: 3301-3317. 10.1038/emboj.2010.212.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  40. Lachke SA, Alkuraya FS, Kneeland SC, Ohn T, Aboukhalil A, Howell GR, Saadi I, Cavallesco R, Yue Y, Tsai AC, Nair KS, Cosma MI, Smith RS, Hodges E, Alfadhli SM, Al-Hajeri A, Shamseldin HE, Behbehani A, Hannon GJ, Bulyk ML, Drack AV, Anderson PJ, John SW, Maas RL: Mutations in the RNA granule component TDRD7 cause cataract and glaucoma. Science. 2011, 331: 1571-1576. 10.1126/science.1195970.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  41. Le Thomas A, Rogers AK, Webster A, Marinov GK, Liao SE, Perkins EM, Hur JK, Aravin AA, Toth KF: Piwi induces piRNA-guided transcriptional silencing and establishment of a repressive chromatin state. Genes Dev. 2013, 27: 390-399. 10.1101/gad.209841.112.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  42. Vasileva A, Tiedau D, Firooznia A, Muller-Reichert T, Jessberger R: Tdrd6 is required for spermiogenesis, chromatoid body architecture, and regulation of miRNA expression. Curr Biol. 2009, 19: 630-639. 10.1016/j.cub.2009.02.047.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  43. Hartenstein AY, Rugendorff A, Tepass U, Hartenstein V: The function of the neurogenic genes during epithelial development in the Drosophila embryo. Development. 1992, 116: 1203-1220.

    CAS  PubMed  Google Scholar 

  44. Clegg NJ, Frost DM, Larkin MK, Subrahmanyan L, Bryant Z, Ruohola-Baker H: maelstrom is required for an early step in the establishment of Drosophila oocyte polarity: posterior localization of grk mRNA. Development. 1997, 124: 4661-4671.

    CAS  PubMed  Google Scholar 

  45. Styhler S, Nakamura A, Swan A, Suter B, Lasko P: vasa is required for GURKEN accumulation in the oocyte, and is involved in oocyte differentiation and germline cyst development. Development. 1998, 125: 1569-1578.

    CAS  PubMed  Google Scholar 

  46. Gillespie DE, Berg CA: Homeless is required for RNA localization in Drosophila oogenesis and encodes a new member of the DE-H family of RNA-dependent ATPases. Genes Dev. 1995, 9: 2495-2508. 10.1101/gad.9.20.2495.

    Article  CAS  PubMed  Google Scholar 

  47. Gonzalez-Reyes A, Elliott H, St Johnston D: Oocyte determination and the origin of polarity in Drosophila: the role of the spindle genes. Development. 1997, 124: 4927-4937.

    CAS  PubMed  Google Scholar 

  48. Schupbach T, Wieschaus E: Female sterile mutations on the second chromosome of Drosophila melanogaster. II. Mutations blocking oogenesis or altering egg morphology. Genetics. 1991, 129: 1119-1136.

    CAS  PubMed Central  PubMed  Google Scholar 

  49. Wilson JE, Connell JE, Macdonald PM: aubergine enhances oskar translation in the Drosophila ovary. Development. 1996, 122: 1631-1639.

    CAS  PubMed  Google Scholar 

  50. Cox DN, Chao A, Baker J, Chang L, Qiao D, Lin H: A novel class of evolutionarily conserved genes defined by piwi are essential for stem cell self-renewal. Genes Dev. 1998, 12: 3715-3727. 10.1101/gad.12.23.3715.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  51. Cox DN, Chao A, Lin H: piwi encodes a nucleoplasmic factor whose activity modulates the number and division rate of germline stem cells. Development. 2000, 127: 503-514.

    CAS  PubMed  Google Scholar 

  52. Spradling AC, Rubin GM: Transposition of cloned P elements into Drosophila germ line chromosomes. Science. 1982, 218: 341-347. 10.1126/science.6289435.

    Article  CAS  PubMed  Google Scholar 

  53. Van Doren M, Williamson AL, Lehmann R: Regulation of zygotic gene expression in Drosophila primordial germ cells. Curr Biol. 1998, 8: 243-246. 10.1016/S0960-9822(98)70091-0.

    Article  CAS  PubMed  Google Scholar 

  54. Lim AK, Tao L, Kai T: piRNAs mediate posttranscriptional retroelement silencing and localization to pi-bodies in the Drosophila germline. J Cell Biol. 2009, 186: 333-342. 10.1083/jcb.200904063.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  55. Pek JW, Lim AK, Kai T: Drosophila Maelstrom ensures proper germline stem cell lineage differentiation by repressing microRNA-7. Dev Cell. 2009, 17: 417-424. 10.1016/j.devcel.2009.07.017.

    Article  CAS  PubMed  Google Scholar 

  56. Handler D, Olivieri D, Novatchkova M, Gruber FS, Meixner K, Mechtler K, Stark A, Sachidanandam R, Brennecke J: A systematic analysis of Drosophila TUDOR domain-containing proteins identifies Vreteno and the Tdrd12 family as essential primary piRNA pathway factors. EMBO J. 2011, 30: 3977-3993. 10.1038/emboj.2011.308.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  57. Klattenhoff C, Xi H, Li C, Lee S, Xu J, Khurana JS, Zhang F, Schultz N, Koppetsch BS, Nowosielska A, Seitz H, Zamore PD, Weng Z, Theurkauf WE: The Drosophila HP1 homolog Rhino is required for transposon silencing and piRNA production by dual-strand clusters. Cell. 2009, 138: 1137-1149. 10.1016/j.cell.2009.07.014.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  58. Klattenhoff C, Bratu DP, McGinnis-Schultz N, Koppetsch BS, Cook HA, Theurkauf WE: Drosophila rasiRNA pathway mutations disrupt embryonic axis specification through activation of an ATR/Chk2 DNA damage response. Dev Cell. 2007, 12: 45-55. 10.1016/j.devcel.2006.12.001.

    Article  CAS  PubMed  Google Scholar 

  59. Liu M, Lim TM, Cai Y: The Drosophila female germline stem cell lineage acts to spatially restrict DPP function within the niche. Sci Signal. 2010, 3: ra57-10.1126/scisignal.2000740.

    Article  PubMed  Google Scholar 

  60. Taft RJ, Glazov EA, Lassmann T, Hayashizaki Y, Carninci P, Mattick JS: Small RNAs derived from snoRNAs. RNA. 2009, 15: 1233-1240. 10.1261/rna.1528909.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

Download references

Acknowledgments

We are grateful to Dr MC Siomi, Dr Haifan Lin and Bloomington Drosophila Stock Center for kindly providing us antibodies and fly stocks, and especially to Dr Dahua Chen for sharing his unpublished anti-SpnE. We thank L Tao for help with the antibody generation, SLM Yang for western blot analysis, TK’s laboratory members for discussions and suggestions, and RSM Lim for critical reading. This work was supported by the Temasek Life Sciences Laboratory and the Singapore Millennium Foundation.

Author information

Authors and Affiliations

  1. Temasek Life Sciences Laboratory, 1 Research Link, National University of Singapore, Singapore, The Republic of Singapore

    Veena S Patil, Amit Anand, Alisha Chakrabarti & Toshie Kai

  2. Department of Biological Sciences, National University of Singapore, Singapore, The Republic of Singapore

    Toshie Kai

  3. School of Biological Sciences, Nanyang Technological University, Singapore, The Republic of Singapore

    Alisha Chakrabarti

  4. Current address: Department of Pediatrics, University of California, San Diego, School of Medicine, 9500 Gilman Drive, La Jolla, 92093, CA, USA

    Veena S Patil

Authors
  1. Veena S Patil
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Amit Anand
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Alisha Chakrabarti
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Toshie Kai
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Toshie Kai.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

VP, AA and TK designed the research; VP, AA and AC performed the research; VP, AA and TK contributed new reagents or analytic tools; VP, AA and TK analyzed the data; VP, AA and TK wrote the paper. All authors read and approved the final manuscript.

Electronic supplementary material

Authors’ original submitted files for images

Rights and permissions

Open Access  This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.

The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.

To view a copy of this licence, visit https://creativecommons.org/licenses/by/4.0/.

The Creative Commons Public Domain Dedication waiver (https://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Patil, V.S., Anand, A., Chakrabarti, A. et al. The Tudor domain protein Tapas, a homolog of the vertebrate Tdrd7, functions in the piRNA pathway to regulate retrotransposons in germline of Drosophila melanogaster. BMC Biol 12, 61 (2014). https://0-doi-org.brum.beds.ac.uk/10.1186/s12915-014-0061-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s12915-014-0061-9

Keywords

BMC Biology

ISSN: 1741-7007

Contact us