Genetics Research International

Genetics Research International / 2012 / Article
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The Role of Epigenetics in Evolution: The Extended Synthesis

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Review Article | Open Access

Volume 2012 |Article ID 324293 | 5 pages |

The “Special” crystal-Stellate System in Drosophila melanogaster Reveals Mechanisms Underlying piRNA Pathway-Mediated Canalization

Academic Editor: Victoria H. Meller
Received14 Jun 2011
Revised18 Aug 2011
Accepted21 Sep 2011
Published15 Dec 2011


The Stellate-made crystals formation in spermatocytes is the phenotypic manifestation of a disrupted crystal-Stellate interaction in testes of Drosophila melanogaster. Stellate silencing is achieved by the piRNA pathway, but many features still remain unknown. Here we outline the important role of the crystal-Stellate modifiers. These have shed light on the piRNA pathways that defend genome integrity against transposons and other repetitive elements in the gonads. In particular, we illustrate the finding that HSP90 participates in the molecular pathways of piRNA production. This observation has relevance for the mechanisms underlying the evolutionary canalization process.

1. The Stellate-Made Crystals in Spermatocytes Are the Phenotypic Manifestation of a Disrupted crystal-Stellate Interaction in Testes of Drosophila melanogaster

The history of the crystal-Stellate system started in 1961 when Meyer and collaborators discovered the presence of crystalline aggregates in primary spermatocytes of D. melanogaster X/O male testes. They also described the morphological differences between needle-shaped and star-shaped crystals [1].

In 1983, Gatti and Pimpinelli provided a detailed cytological description of the chromosome. They showed that the hll region contains the genetic determinants for normal chromosome behavior during male meiosis and for the suppression of Stellate-made crystals formation in spermatocytes [2]. This region was called the Suppressor of Stellate [Su(Ste)] locus, also referred to as crystal (cry) [3]; in this paper we use “crystal.”

Afterwards, different groups established that both the morphology of the crystalline aggregates and the severity of the meiotic defects in X/O and males depend on the Stellate (Ste) locus on the chromosome [46]. Two regions containing clustered Stellate elements have been identified on the chromosome: 12E1 in euchromatin and h27 in heterochromatin. Stellate and crystal are both repetitive sequences and they share sequence homology [68].

At the molecular level, the loss of the crystal region results in the production of a testes-specific Stellate mRNA of 750 nucleotides in length. The product of this mRNA is the Stellate protein [8, 9]. In 1995 there was a fundamental discovery: the Stellate protein is the main component of the crystals in the primary spermatocytes [10] and Figure 1.

2. The Regulation of the crystal-Stellate Interaction

The first indication about the mechanism that regulates the interaction between crystal and Stellate sequences was obtained in 2001; the Stellate silencing was associated with the presence of small RNAs, 24–29 nt long, homologous to crystal and Stellate sequences [11]. These were named rasiRNAs (repeat-associated small interfering RNAs) [12].

The detailed analysis of the crystal-rasiRNAs in fly testes demonstrated the existence of a specific RNAi pathway in the germline that silences repetitive sequences such as Stellate and transposable elements [13]. It was also demonstrated that rasiRNAs show differences in structure compared to other classes of small noncoding RNAs, such as siRNAs and miRNAs and their biogenesis is Dicer-independent [13]. The rasiRNAs work associated with the Piwi subfamily of the Argonaute proteins, Aubergine, Ago3, and Piwi. rasiRNAs were subsequently designated as Piwi-interacting RNAs or piRNAs [13]. The studies on the crystal-Stellate system have been therefore crucial for the discovery of the piRNA pathway.

In 2007, two independent groups used a deep sequencing strategy to identify small RNAs bound to each of the three Piwi proteins in fly ovaries. Their expectation was that this approach would reveal how piRNAs were made and how they function. They demonstrated that piRNAs arise from a few genomic sites, grouped in clusters that produce small RNAs that silence many transposons [14, 15]. In fly testes, the most abundant Aubergine-associated piRNAs (~70%) correspond to crystal antisense transcripts [16].

3. The piRNA Pathways in the Fly Ovaries

Studies on the sequences of the small RNAs associated to Piwi subclade proteins carried out in 2006 and 2007 by the Hannon, Zamore, and Siomi groups have been crucial to formulation of a model for the biogenesis and the function of the piRNAs in the germline [1316]. The proposed model, called the “ping-pong” model, requires a primary piRNA, whose biogenesis has not yet been elucidated, bound by Aubergine or Ago3. In particular, Aub binds an antisense piRNA and cleaves the sense transcript from an active transposon; transcript cleavage produces a sense piRNA that is loaded onto Ago3. This Ago3-piRNA complex binds complementary transcripts and initiates the production of piRNAs by an amplification loop [14]. The piRNAs originated by this mechanism are now called “secondary” piRNAs and they exhibit specific signatures consisting of the adenine at the 10th position of the sense piRNAs, which is able to base pair with the initial uracil of the antisense piRNAs [14, 15].

Identification of ago3 mutants led to the discovery of two different piRNA pathways in the fly ovary: one in the somatic cells of the ovary and the other in the germline cells. The somatic pathway, called “primary piRNA pathway,” involves Piwi, and it does not require an amplification loop. This pathway regulates the transposons belonging to the so-called “somatic” group [17, 18].

4. The piRNA Pathways in Fly Testes and Open Questions

Deep sequencing of piRNAs bound to Piwi-subfamily proteins associated to genetic studies, supplied thousands of data about almost all the piRNAs sequence biogenesis and orientation produced in testes [16, 19].

Although the overall structure of the crystal and Stellate loci remains unclear, regions of homology between crystal and Stellate piRNAs, and repeat monomers from each of these loci has been summarized in the scheme depicted in Figure 2. The position of several piRNAs on the crystal and Stellate sequences, their orientation and the Piwi protein(s) to which they are bound are indicated. Detailed information on the sequences of crystal (Z11734) and Stellate euchromatic sequences (X15799), depicting the location of piRNAs, are shown in Figure 1S (see Figure 1S in supplementary material available online at In light of this map we note that almost all the crystal-specific piRNAs come from the region, depicted in purple, of homology with Stellate sequences. These are predominantly “antisense” as already reported [11, 12, 14, 16, 19]. However, Stellate-specific piRNAs, whether euchromatic or heterochromatic, are predominantly in the “sense” orientation (Figure 2).

The majority of these piRNAs do not show the ping-pong signature. There are only 3 pairs exhibiting the A at the 10th position of the “sense” piRNA, and these “sense” piRNAs show 2 or 3 mismatches with Stellate euchromatic and heterochromatic sequences. Therefore, they cannot be considered canonical ping-pong pairs [Figure 1S(a)]. The crystal-specific piRNA, reported to be the most abundant one in testes, is only antisense [19], Figure 2.

For all the reasons reported above, we hypothesize that different though interconnected pathways exist to silence crystal and Stellate sequences. crystal- and Stellate-specific piRNAs cooperate in some way to silence the Stellate euchromatic and heterochromatic sequences that produce the Stellate protein (“active elements”) [10, 20]. These different pathways could be present in both the somatic and germline tissues of testes.

In support of these considerations, we refer to the previous data on the silencing of another class of repetitive sequences in testes. In fact, a second large class of piRNAs associated with Aubergine in the testes is derived from a short repeated region, termed AT-chX, on the X chromosome [16]. These piRNAs are predominantly antisense. Only one pair with ping-pong signatures was found among all sequenced AT-chX piRNAs. These remarks confirm that the ping pong is not the only piRNA pathways operating in the silencing of these repetitive sequences in testes [19].

5. Mutants Affecting the crystal-Stellate Interaction Clarify Unknown Aspects of the piRNA Pathways in Testes

Mutations in piRNA-pathway genes, such as aubergine, ago3, spindle E, armitage, zucchini, and squash, lead to the formation of the Stellate-made crystals in spermatocytes [17, 2124].

spindle-E encodes a member of the DExH family of ATPases with a Tudor domain. Mutations in this gene are known to impair Stellate and transposon silencing in the Drosophila germline. In ovaries spindle-E acts specifically in germ cells and in the ping-pong cycle [18, 22, 25].

Armitage encodes a homolog of the Arabidopsis SDE3, an RNA helicase that is involved in RNAi. Mutations in armitage affect translational repression and localization of oskar mRNA, block RNAi in Drosophila oocytes, and impair Stellate silencing in testes [23, 26]. In ovaries, armitage acts in the primary piRNA pathway [18, 27, 28]. zucchini was identified in a screen for female sterile mutations, and causes dorsoventral patterning defects. This gene encodes a nuclease. Mutations in zucchini lead to formation of Stellate crystals [24]. In ovaries zucchini mutations specifically decrease the piRNA levels in somatic ovarian cells [18].

In Table 1, we listed some of the modifiers of the crystal-Stellate interaction that have been related to the piRNA pathways in gonads. Mutants of genes implicated either in the primary piRNA pathway, excepting piwi, or in the secondary ping-pong amplification pathway show crystals in their spermatocytes.

GenesCrystalsFunctionPing pong*References

Aubergine+Piwi protein− −/+[1419, 21]
Ago3+Piwi protein− −/+[1719]
PiwiPiwi protein+[1318]

Spindle-E+RNA helicase− −/+[18, 22, 25]
Squash+Tudor-domain nuclease+[24]

Armitage+RNA helicase+[18, 23, 2628]

hsp83+Heat-shock proteinnd[29]

*“+” indicates that the ping pong is functional in the mutant.

After all, we are convinced that the molecular mechanisms, underlying the piRNA pathways, are not completely understood and that there are more players to be discovered in both the somatic and germline-specific piRNA pathways. The genetic characterization of known and still unknown components, combined with the deep sequencing strategy of the piRNAs bound to specific Piwi proteins, will help us in understanding the piRNAs production and function in the Drosophila testes. Because Stellate-made crystals are symptomatic of a disrupted crystal-Stellate interaction, they allow the identification of new genetic components of the piRNAs pathway. An emblematic example is the discovery that the hsp83 gene participates in piRNA.

6. hsp83scratch, an Unexpected crystal-Stellate Modifier

The hsp83 gene encodes HSP90 protein, a molecular chaperone involved in several cellular processes and developmental pathways [3033]. We have recently demonstrated that primary spermatocytes of hsp83scratch  homozygous mutant males exhibit Stellate-made crystalline aggregates, suggesting a role for this protein in the piRNA-mediated mechanisms. We also demonstrated that hsp83scratch  affects the biogenesis of the crystal/Stellate-specific piRNAs and transposon piRNAs in testes. We went on to demonstrate that the effect of HSP90 in morphological variations is due, at least in part, to activation of transposons causing de novo mutations [29]. Among the hsp83 mutant flies showing morphological abnormalities, we selected one exhibiting a Scutoid-like phenotype and demonstrated that this phenotype is caused by the insertion of an element-like transposon in the noc gene of this fly.

The role of HSP90 in piRNAs-mediated silencing is in addition to the “buffering” role on the genetic cryptic variation initially put forth by Rutherford and Lindquist [34] as the molecular explanation for the Waddington’s “canalization” process.

Canalization is the resistance of an organism to phenotypic variation during development, in the presence of genetic and environmental changes. This “phenotype robustness” is due to buffering mechanisms. Severe perturbations, which reduce buffering, produce heritable phenotypic variants that can be canalized by a genetic assimilation process [35]. An interesting aspect to investigate is if, and how, the reduction of HSP90 causes a stress response-like activation of mobile elements, creating a link between environmental changes and genomic variation.

Further mechanisms could be involved in increasing the phenotypic variations underlying evolution. One of these could be related to HSP90-mediated epigenetic chromatin modifications [36, 37].


The authors thank S. Pimpinelli for helpful discussions and comments on the paper.

Supplementary Materials

Precise localization of specific piRNAs on the Stellate (X15899) and crystal (Z11734) sequences. In order to visualize the region of the Stellate and crystal sequences that share homology with the most abundant piRNAs related to them (Nagao et al. 2010), we precisely localized some of these piRNAs on the sequences.

We selected two emblematic sequences for Stellate (X15899) and crystal (Z11734). We also reported their orientation and the Argonaute proteins which the reported piRNAs are bound to.

  1. Supplementary Figure 1
  2. Supplementary Figure 2


  1. G. Meyer, O. Hess, and W. Beermann, “Phasenspezifische funktionsstrukturen in spermatocytenkernen von Drosophila melanogaster und ihre abhangigkeit vom Y chromosom,” Chromosoma, vol. 12, no. 1, pp. 676–716, 1961. View at: Publisher Site | Google Scholar
  2. M. Gatti and S. Pimpinelli, “Cytological and genetic analysis of the Y chromosome of Drosophila melanogaster. I. Organization of the fertility factors,” Chromosoma, vol. 88, no. 5, pp. 349–373, 1983. View at: Google Scholar
  3. S. Pimpinelli, S. Bonaccorsi, M. Gatti, and L. Sandler, “The peculiar genetic organization of Drosophila heterochromatin,” Trends in Genetics, vol. 2, pp. 17–20, 1986. View at: Google Scholar
  4. R. W. Hardy, D. L. Lindsley, and K. J. Livak, “Cytogenetic analysis of a segment of the Y chromosome of Drosophila melanogaster,” Genetics, vol. 107, no. 4, pp. 591–610, 1984. View at: Google Scholar
  5. K. J. Livak, “Organization and mapping of a sequence on the Drosophila melanogaster X and Y chromosomes that is transcribed during spermatogenesis,” Genetics, vol. 107, no. 4, pp. 611–634, 1984. View at: Google Scholar
  6. G. Palumbo, S. Bonaccorsi, L. G. Robbins, and S. Pimpinelli, “Genetic analysis of Stellate elements of Drosophila melanogaster,” Genetics, vol. 138, no. 4, pp. 1181–1197, 1994. View at: Google Scholar
  7. A. V. Tulin, G. Kogan, D. Filipp, M. D. Balakireva, and V. A. Gvozdev, “Heterochromatic Stellate gene cluster in Drosophila melanogaster: structure and molecular evolution,” Genetics, vol. 146, no. 1, pp. 253–262, 1997. View at: Google Scholar
  8. P. Tritto, V. Specchia, L. Fanti et al., “Structure, regulation and evolution of the crystal-Stellate system of Drosophila,” Genetica, vol. 117, no. 2-3, pp. 247–257, 2003. View at: Publisher Site | Google Scholar
  9. K. J. Livak, “Detailed structure of the Drosophila melanogaster Stellate genes and their transcripts,” Genetics, vol. 124, no. 2, pp. 303–316, 1990. View at: Google Scholar
  10. M. P. Bozzetti, S. Massari, P. Finelli et al., “The Ste locus, a component of the parasitic cry-Ste system of Drosophila melanogaster, encodes a protein that forms crystals in primary spermatocytes and mimics properties of the β subunit of casein kinase 2,” Proceedings of the National Academy of Sciences of the United States of America, vol. 92, no. 13, pp. 6067–6071, 1995. View at: Publisher Site | Google Scholar
  11. A. A. Aravin, N. M. Naumova, A. V. Tulin, V. V. Vagin, Y. M. Rozovsky, and V. A. Gvozdev, “Double-stranded RNA-mediated silencing of genomic tandem repeats and transposable elements in the D. melanogaster germline,” Current Biology, vol. 11, no. 13, pp. 1017–1027, 2001. View at: Publisher Site | Google Scholar
  12. A. A. Aravin, M. Lagos-Quintana, A. Yalcin et al., “The small RNA profile during Drosophila melanogaster development,” Developmental Cell, vol. 5, no. 2, pp. 337–350, 2003. View at: Publisher Site | Google Scholar
  13. V. V. Vagin, A. Sigova, C. Li, H. Seitz, V. Gvozdev, and P. D. Zamore, “A distinct small RNA pathway silences selfish genetic elements in the germline,” Science, vol. 313, no. 5785, pp. 320–324, 2006. View at: Publisher Site | Google Scholar
  14. J. Brennecke, A. A. Aravin, A. Stark et al., “Discrete small RNA-generating loci as master regulators of transposon activity in drosophila,” Cell, vol. 128, no. 6, pp. 1–15, 2007. View at: Publisher Site | Google Scholar
  15. L. S. Gunawardane, K. Saito, K. M. Nishida et al., “A slicer-mediated mechanism for repeat-associated siRNA 5' end formation in Drosophila,” Science, vol. 315, no. 5818, pp. 1587–1590, 2007. View at: Publisher Site | Google Scholar
  16. K. M. Nishida, K. Saito, T. Mori et al., “Gene silencing mechanisms mediated by Aubergine-piRNA complexes in Drosophila male gonad,” RNA, vol. 13, no. 11, pp. 1911–1922, 2007. View at: Publisher Site | Google Scholar
  17. C. Li, V. Vagin, S. Lee et al., “Collapse of germline piRNAs in the absence of argonaute 3 reveals somatic piRNAs in flies,” Cell, vol. 137, no. 3, pp. 509–521, 2009. View at: Publisher Site | Google Scholar
  18. C. D. Malone, J. Brennecke, M. Dus et al., “Specialized piRNA pathways act in germline and somatic tissues of the Drosophila ovary,” Cell, vol. 137, no. 3, pp. 522–535, 2009. View at: Publisher Site | Google Scholar
  19. A. Nagao, T. Mituyama, H. Huang, D. Chen, M. C. Siomi, and H. Siomi, “Biogenesis pathways of piRNAs loaded onto AGO3 in the Drosophila testis,” RNA, vol. 16, no. 12, pp. 2503–2515, 2010. View at: Publisher Site | Google Scholar
  20. R. N. Kotelnikov, M. S. Klenov, Y. M. Rozovsky, L. V. Olenina, M. V. Kibanov, and V. A. Gvozdev, “Peculiarities of piRNA-mediated post-transcriptional silencing of Stellate repeats in testes of Drosophila melanogaster,” Nucleic Acids Research, vol. 37, no. 10, pp. 3254–3263, 2009. View at: Publisher Site | Google Scholar
  21. A. Schmidt, G. Palumbo, M. P. Bozzetti et al., “Genetic and molecular characterization of sting, a gene involved in crystal formation and meiotic drive in the male germ line of Drosophila melanogaster,” Genetics, vol. 151, no. 2, pp. 749–760, 1999. View at: Google Scholar
  22. W. Stapleton, S. Das, and B. McKee, “A role of the Drosophila homeless gene in repression of Stellate in male meiosis,” Chromosoma, vol. 110, no. 3, pp. 228–240, 2001. View at: Google Scholar
  23. Y. Tomari, T. Du, B. Haley et al., “RISC assembly defects in the Drosophila RNAi mutant armitage,” Cell, vol. 116, no. 6, pp. 831–841, 2004. View at: Publisher Site | Google Scholar
  24. A. Pane, K. Wehr, and T. Schüpbach, “Zucchini and squash encode two putative nucleases required for rasiRNA production in the Drosophila germline,” Developmental Cell, vol. 12, no. 6, pp. 851–862, 2007. View at: Publisher Site | Google Scholar
  25. A. K. Lim and T. Kai, “Unique germ-line organelle, nuage, functions to repress selfish genetic elements in Drosophila melanogaster,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 16, pp. 6714–6719, 2007. View at: Publisher Site | Google Scholar
  26. H. A. Cook, B. S. Koppetsch, J. Wu, and W. E. Theurkauf, “The Drosophila SDE3 homolog armitage is required for oskar mRNA silencing and embryonic axis specification,” Cell, vol. 116, no. 6, pp. 817–829, 2004. View at: Publisher Site | Google Scholar
  27. D. Olivieri, M. M. Sykora, R. Sachidanandam, K. Mechtler, and J. Brennecke, “An in vivo RNAi assay identifies major genetic and cellular requirements for primary piRNA biogenesis in Drosophila,” The EMBO Journal, vol. 29, no. 19, pp. 3301–3317, 2010. View at: Publisher Site | Google Scholar
  28. K. Saito, H. Ishizu, M. Komai et al., “Roles for the Yb body components Armitage and Yb in primary piRNA biogenesis in Drosophila,” Genes and Development, vol. 24, no. 22, pp. 2493–2498, 2010. View at: Publisher Site | Google Scholar
  29. V. Specchia, L. Piacentini, P. Tritto et al., “Hsp90 prevents phenotypic variation by suppressing the mutagenic activity of transposons,” Nature, vol. 463, no. 7281, pp. 662–665, 2010. View at: Publisher Site | Google Scholar
  30. D. Ding, S. M. Parkhurst, S. R. Halsell, and H. D. Lipshitz, “Dynamic Hsp83 RNA localization during Drosophila oogenesis and embryogenesis,” Molecular and Cellular Biology, vol. 13, no. 6, pp. 3773–3781, 1993. View at: Google Scholar
  31. T. Cutforth and G. M. Rubin, “Mutations in Hsp83 and cdc37 impair signaling by the sevenless receptor tyrosine kinase in Drosophila,” Cell, vol. 77, no. 7, pp. 1027–1036, 1994. View at: Publisher Site | Google Scholar
  32. F. U. Hartl, “Molecular chaperones in cellular protein folding,” Nature, vol. 381, no. 6583, pp. 571–580, 1996. View at: Publisher Site | Google Scholar
  33. A. van der Straten, C. Rommel, B. Dickson, and E. Hafen, “The heat shock protein 83 (Hsp83) is required for Raf-mediated signalling in Drosophila,” EMBO Journal, vol. 16, no. 8, pp. 1961–1969, 1997. View at: Publisher Site | Google Scholar
  34. S. L. Rutherford and S. Lindquist, “Hsp90 as a capacitor for morphological evolution,” Nature, vol. 396, no. 6709, pp. 336–342, 1998. View at: Publisher Site | Google Scholar
  35. C. H. Waddington, “Canalization of development and the inheritance of acquired characters,” Nature, vol. 150, no. 3811, pp. 563–565, 1942. View at: Google Scholar
  36. V. Sollars, X. Lu, L. Xiao, X. Wang, M. D. Garfinkel, and D. M. Ruden, “Evidence for an epigenetic mechanism by which Hsp90 acts as a capacitor for morphological evolution,” Nature Genetics, vol. 33, no. 1, pp. 70–74, 2003. View at: Publisher Site | Google Scholar
  37. V. K. Gangaraju, H. Yin, M. M. Weiner, J. Wang, X. A. Huang, and H. Lin, “Drosophila Piwi functions in Hsp90-mediated suppression of phenotypic variation,” Nature Genetics, vol. 43, pp. 153–158, 2011. View at: Publisher Site | Google Scholar

Copyright © 2012 Maria Pia Bozzetti et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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