A regulatory circuit for piwi by the large Maf gene traffic jam in Drosophila (original) (raw)

Nature volume 461, pages 1296–1299 (2009)Cite this article

Abstract

PIWI-interacting RNAs (piRNAs) silence retrotransposons in Drosophila germ lines by associating with the PIWI proteins Argonaute 3 (AGO3), Aubergine (Aub) and Piwi1,2. piRNAs in Drosophila are produced from intergenic repetitive genes and piRNA clusters by two systems: the primary processing pathway and the amplification loop1,2,3,4,5,6,7. The amplification loop occurs in a Dicer-independent, PIWI-Slicer-dependent manner3,4,8. However, primary piRNA processing remains elusive. Here we analysed piRNA processing in a Drosophila ovarian somatic cell line where Piwi, but not Aub or AGO3, is expressed; thus, only the primary piRNAs exist. In addition to flamenco, a Piwi-specific piRNA cluster3, traffic jam (tj)9, a large Maf gene, was determined as a new piRNA cluster. piRNAs arising from tj correspond to the untranslated regions of tj messenger RNA and are sense-oriented. piRNA loading on to Piwi may occur in the cytoplasm. zucchini10, a gene encoding a putative cytoplasmic nuclease, is required for _tj_-derived piRNA production. In tj and piwi mutant ovaries, somatic cells fail to intermingle with germ cells and Fasciclin III is overexpressed. Loss of tj abolishes Piwi expression in gonadal somatic cells. Thus, in gonadal somatic cells, tj gives rise simultaneously to two different molecules: the TJ protein, which activates Piwi expression, and piRNAs, which define the Piwi targets for silencing.

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Figure 1: Piwi in OSCs is associated with endogenous small RNAs.

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Figure 2: Piwi-associated piRNAs in OSCs.

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Figure 3: Involvement of zuc in the tj –piRNA production pathway.

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Figure 4: Phenotypes of tj and piwi mutant ovaries and testes.

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Accession codes

Primary accessions

Gene Expression Omnibus

Data deposits

Small RNA sequences have been deposited at the GEO database under accession number GSE15137.

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Acknowledgements

We thank Y. Niki, D. Godt, H. Lin, E. Matunis, S. Kobayashi, Y. Kitadate, Y. Kageyama and H. Sano for providing reagents. We also thank Bloomington and Kyoto Drosophila Stock Center for the supply of Drosophila strains. We thank K. Yamada, E. Hattori, K. M. Nishida and T. N. Okada for technical assistance; S. Takahashi and K. Kataoka for discussions and suggestions; and other members of the Siomi laboratory for discussions and comments on the manuscript. We also thank K. Greer and D. McGowan for encouragement. This work was supported by MEXT grants to H.S. and NEDO (New Energy and Industrial Technology Development Organization) grants to M.C.S., T.M. and K.A. M.C.S. is supported by CREST from JST. M.C.S. is Associate Professor of Global COE for Human Metabolomics Systems Biology by MEXT.

Author Contributions K.S., S.I., Y.K. and H.K. conducted biochemical experiments. T.M., Y.O., E.S. and K.A. performed bioinformatics. K.S., T.M., H.S. and M.C.S designed experiments, interpreted data and prepared the manuscript.

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Authors and Affiliations

  1. Keio University School of Medicine, Tokyo 160-8582, Japan
    Kuniaki Saito, Sachi Inagaki, Yoshinori Kawamura, Hazuki Kotani, Haruhiko Siomi & Mikiko C. Siomi
  2. Computational Biology Research Center (CBRC), National Institute of Advanced Industrial Science and Technology (AIST), Tokyo 135-0064, Japan
    Toutai Mituyama & Kiyoshi Asai
  3. Institute of Health Biosciences University of Tokushima, Tokushima 770-8503, Japan
    Yoshinori Kawamura
  4. Department of Life Sciences, Information and Mathematical Science Laboratory, Inc., Tokyo 112-0012, Japan
    Yukiteru Ono
  5. Japan Biological Informatics Consortium (JBIC), Tokyo 135-8073, Japan
    Eri Sakota
  6. Graduate School of Frontier Sciences, University of Tokyo, Chiba 277-8583, Japan
    Kiyoshi Asai
  7. JST, CREST, Saitama 332-0012, Japan
    Mikiko C. Siomi

Authors

  1. Kuniaki Saito
  2. Sachi Inagaki
  3. Toutai Mituyama
  4. Yoshinori Kawamura
  5. Yukiteru Ono
  6. Eri Sakota
  7. Hazuki Kotani
  8. Kiyoshi Asai
  9. Haruhiko Siomi
  10. Mikiko C. Siomi

Corresponding authors

Correspondence toHaruhiko Siomi or Mikiko C. Siomi.

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Saito, K., Inagaki, S., Mituyama, T. et al. A regulatory circuit for piwi by the large Maf gene traffic jam in Drosophila.Nature 461, 1296–1299 (2009). https://doi.org/10.1038/nature08501

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Editorial Summary

A regulatory circuit for Piwi

A class of small RNAs, piRNAs, interact with PIWI domain-containing Argonaute proteins. Germline piRNAs derive from repetitive DNA and are produced by an amplification process. Recently piRNAs have also been found to be encoded by protein-coding genes in somatic cells. In this work, Siomi and colleagues show that the traffic jam (tj) locus, encoding the Maf transcription factor, encodes a piRNA cluster. These piRNAs are produced in the cytoplasm without amplification, and target FasIII for silencing. Maf itself activates Piwi expression. Thus, the tj locus encodes both an enhancer of Piwi and the piRNAs that interact with Piwi.