Defensin-like polypeptide LUREs are pollen tube attractants secreted from synergid cells (original) (raw)
- Letter
- Published: 19 March 2009
- Hiroki Tsutsui1 na1,
- Keiko Shiina1,
- Stefanie Sprunck2,
- Hidenori Takeuchi1,
- Ryoko Yui1,
- Ryushiro D. Kasahara1,
- Yuki Hamamura1,
- Akane Mizukami1,
- Daichi Susaki1,
- Nao Kawano1,
- Takashi Sakakibara1,
- Shoko Namiki1,
- Kie Itoh3,
- Kurataka Otsuka4,
- Motomichi Matsuzaki4,
- Hisayoshi Nozaki4,
- Tsuneyoshi Kuroiwa5,
- Akihiko Nakano4,6,
- Masahiro M. Kanaoka1,
- Thomas Dresselhaus2,
- Narie Sasaki1 na1 &
- …
- Tetsuya Higashiyama1 na1
Nature volume 458, pages 357–361 (2009)Cite this article
- 12k Accesses
- 467 Citations
- 11 Altmetric
- Metrics details
Abstract
For more than 140 years, pollen tube guidance in flowering plants has been thought to be mediated by chemoattractants derived from target ovules1. However, there has been no convincing evidence of any particular molecule being the true attractant that actually controls the navigation of pollen tubes towards ovules. Emerging data indicate that two synergid cells on the side of the egg cell emit a diffusible, species-specific signal to attract the pollen tube at the last step of pollen tube guidance1,2,3. Here we report that secreted, cysteine-rich polypeptides (CRPs) in a subgroup of defensin-like proteins are attractants derived from the synergid cells. We isolated synergid cells of Torenia fournieri, a unique plant with a protruding embryo sac, to identify transcripts encoding secreted proteins as candidate molecules for the chemoattractant(s). We found two CRPs, abundantly and predominantly expressed in the synergid cell, which are secreted to the surface of the egg apparatus. Moreover, they showed activity in vitro to attract competent pollen tubes of their own species and were named as LUREs. Injection of morpholino antisense oligomers against the LUREs impaired pollen tube attraction, supporting the finding that LUREs are the attractants derived from the synergid cells of T. fournieri.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Additional access options:
Similar content being viewed by others
References
- Higashiyama, T. & Hamamura, Y. Gametophytic pollen tube guidance. Sex. Plant Reprod. 21, 17–26 (2008)
Article Google Scholar - Higashiyma, T. et al. Pollen tube attraction by the synergid cell. Science 293, 1480–1483 (2001)
Article ADS Google Scholar - Punwani, J. A. & Drews, G. N. Development and function of the synergid cell. Sex. Plant Reprod. 21, 7–15 (2008)
Article Google Scholar - Higashiyama, T. et al. Species preferentiality of the pollen tube attractant derived from the synergid cell of Torenia fournieri. Plant Physiol. 142, 481–491 (2006)
Article CAS Google Scholar - Imre, K. & Kristof, Z. Isolation and osmotic relations of developing megagametophytes of Torenia fournieri. Sex. Plant Reprod. 12, 152–157 (1999)
Article Google Scholar - Silverstein, K. A. et al. Small cysteine-rich peptides resembling antimicrobial peptides have been under-predicted in plants. Plant J. 51, 262–280 (2007)
Article CAS Google Scholar - Punwani, J. A., Rabiger, D. S. & Drews, G. N. MYB98 positively regulates a battery of synergid-expressed genes encoding filiform apparatus-localized proteins. Plant Cell 19, 2557–2568 (2007)
Article CAS Google Scholar - Jones-Rhoades, M. W., Borevitz, J. O. & Preuss, D. Genome-wide expression profiling of the Arabidopsis female gametophyte identifies families of small, secreted proteins. PLoS Genet. 3, 1848–1861 (2007)
Article CAS Google Scholar - Cordts, S. et al. ZmES genes encode peptides with structural homology to defensins and are specifically expressed in the female gametophyte of maize. Plant J. 25, 103–114 (2001)
Article CAS Google Scholar - Yang, H., Kaur, N., Kiriakopolos, S. & McCormick, S. EST generation and analyses towards identifying female gametophyte-specific genes in Zea mays L. Planta 224, 1004–1014 (2006)
Article CAS Google Scholar - Kasahara, R. D. et al. MYB98 is required for pollen tube guidance and synergid cell differentiation in Arabidopsis. Plant Cell 17, 2981–2992 (2005)
Article CAS Google Scholar - Silverstein, K. A., Graham, M. A., Paape, T. D. & VandenBosch, K. A. Genome organization of more than 300 defensin-like genes in Arabidopsis. Plant Physiol. 138, 600–610 (2005)
Article CAS Google Scholar - Cornet, B. et al. Refined three-dimensional solution structure of insect defensin A. Structure 3, 435–448 (1995)
Article CAS Google Scholar - Yount, N. Y. & Yeaman, M. R. Multidimensional signatures in antimicrobial peptides. Proc. Natl Acad. Sci. USA 101, 7363–7368 (2004)
Article ADS CAS Google Scholar - Higashiyama, T., Kuroiwa, H., Kawano, S. & Kuroiwa, T. Guidance in vitro of the pollen tube to the naked embryo sac of Torenia fournieri. Plant Cell 10, 2019–2031 (1998)
Article CAS Google Scholar - Takayama, S. et al. Direct ligand–receptor complex interaction controls Brassica self-incompatibility. Nature 413, 534–538 (2001)
Article ADS CAS Google Scholar - Karkare, S. & Bhatnagar, D. Promising nucleic acid analogs and mimics: characteristic features and applications of PNA, LNA, and morpholino. Appl. Microbiol. Biotechnol. 71, 575–586 (2006)
Article CAS Google Scholar - Han, Y. Z., Huang, B. Q., Zee, S. Y. & Yuan, M. Symplastic communication between the central cell and the egg apparatus cells in the embryo sac of Torenia fournieri Lind. before and during fertilization. Planta 211, 158–162 (2000)
Article CAS Google Scholar - Kim, S. et al. Chemocyanin, a small basic protein from the lily stigma, induces pollen tube chemotropism. Proc. Natl Acad. Sci. USA 100, 16125–16130 (2003)
Article ADS CAS Google Scholar - Wolters-Arts, M., Lush, W. M. & Mariani, C. Lipids are required for directional pollen-tube growth. Nature 392, 818–821 (1998)
Article ADS CAS Google Scholar - Palanivelu, R., Brass, L., Edlund, A. F. & Preuss, D. Pollen tube growth and guidance is regulated by POP2, an Arabidopsis gene that controls GABA levels. Cell 114, 47–59 (2003)
Article CAS Google Scholar - Márton, M. L., Cordts, S., Broadhvest, J. & Dresselhaus, T. Micropylar pollen tube guidance by EGG APPARATUS 1 of maize. Science 307, 573–576 (2005)
Article ADS Google Scholar - Park, S. Y. et al. A lipid transfer-like protein is necessary for lily pollen tube adhesion to an in vitro stylar matrix. Plant Cell 12, 151–163 (2000)
Article CAS Google Scholar - Doughty, J. et al. PCP-A1, a defensin-like Brassica pollen coat protein that binds the S locus glycoprotein, is the product of gametophytic gene expression. Plant Cell 10, 1333–1347 (1998)
Article CAS Google Scholar - Cheung, A. Y. & Wu, H. M. Pollen tube guidance—right on target. Science 293, 1441–1442 (2001)
Article CAS Google Scholar - Higashiyama, T. The synergid cell: attractor and acceptor of the pollen tube for double fertilization. J. Plant Res. 115, 149–160 (2002)
Article Google Scholar - Márton, M. L. & Dresselhaus, T. A comparison of early molecular fertilization mechanisms in animals and flowering plants. Sex. Plant Reprod. 21, 37–52 (2008)
Article Google Scholar - Berger, F., Hamamura, Y., Ingouff, M. & Higashiyama, T. Double fertilization — caught in the act. Trends Plant Sci. 13, 437–443 (2008)
Article CAS Google Scholar - Escobar-Restrepo, J. M. et al. The FERONIA receptor-like kinase mediates male–female interactions during pollen tube reception. Science 317, 656–660 (2007)
Article ADS CAS Google Scholar - Sprunck, S. et al. The transcript composition of egg cells changes significantly following fertilization in wheat (Triticum aestivum L.). Plant J. 41, 660–672 (2005)
Article CAS Google Scholar - Higashiyama, T. & Inatsugi, R. Comparative analyses of biological models used in the study of pollen tube growth. Plant Cell Monogr. 3, 265–286 (2006)
Article CAS Google Scholar - Ingouff, M. et al. Distinct dynamics of HISTONE3 variants between the two fertilization products in plants. Curr. Biol. 17, 1032–1037 (2007)
Article CAS Google Scholar
Acknowledgements
We thank T. Suzuki for help with the analysis of the EST sequences, S. Takayama for providing chemically synthesized and refolded SP11 peptides, W. Uchida for checking the diameter of the glass needles for microinjection by scanning electron microscopy and N. Iwata for assistance in preparing plant materials. This work was supported in part by a Grant-in-Aid for Young Scientists (Start-up), Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan (20870020 to M.M.K.); a Grant-in-Aid for Creative Scientific Research, MEXT, Japan (18GS0314-01 to N.S.); a grant from Yamada Science Foundation, Japan (to T.H.); a Grant-in-Aid for Scientific Research (B), MEXT, Japan (19370017 to T.H.); a Grant-in-Aid for Scientific Research on Priority Areas (18075004 to T.H.), and PRESTO project, Japan Science and Technology Agency, Japan (to T.H.).
Author Contributions S.O., N.S. and T.H. developed methods to purify and assay recombinant LUREs. H.Tsutsui and T.H. developed methods for the microinjection of the MO oligos and performed the RT–PCR analysis. K.S., N.S. and M.M.K. developed immunological methods to detect LUREs. T.H., S.S. and T.D. constructed the cDNA library of the synergid cell of T. fournieri and directed the EST analysis. H.Takeuchi., R.Y., R.D.K., Y.H., A.M., D.S., N.K., T.S., K.I., K.O., M.M., H.N. and M.M.K. assembled and analysed the EST sequences. S.N. constructed expression vectors and purified recombinant LUREs. T.K., A.N., T.D., M.M.K., N.S. and T.H. contributed to the experimental design. T.H. directed the project and wrote the paper with input from co-authors.
Author information
Author notes
- Satohiro Okuda, Hiroki Tsutsui, Narie Sasaki and Tetsuya Higashiyama: These authors contributed equally to this work.
Authors and Affiliations
- Division of Biological Science, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8602, Japan,
Satohiro Okuda, Hiroki Tsutsui, Keiko Shiina, Hidenori Takeuchi, Ryoko Yui, Ryushiro D. Kasahara, Yuki Hamamura, Akane Mizukami, Daichi Susaki, Nao Kawano, Takashi Sakakibara, Shoko Namiki, Masahiro M. Kanaoka, Narie Sasaki & Tetsuya Higashiyama - Cell Biology/Plant Physiology, University of Regensburg, Universitätsstraße 31, 93053 Regensburg, Germany
Stefanie Sprunck & Thomas Dresselhaus - Department of Integrated Biosciences, Graduate School of Frontier Sciences, University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8562, Japan,
Kie Itoh - Department of Biological Sciences, Graduate School of Science, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan,
Kurataka Otsuka, Motomichi Matsuzaki, Hisayoshi Nozaki & Akihiko Nakano - Research Information Center of Extremophile, Graduate School of Science, Rikkyo (Saint Paul’s) University, Nishi-Ikebukuro, Tokyo 171-8501, Japan,
Tsuneyoshi Kuroiwa - Molecular Membrane Biology Laboratory, RIKEN Advanced Science Institute, Hirosawa, Wako, Saitama 351-0198, Japan,
Akihiko Nakano
Authors
- Satohiro Okuda
You can also search for this author inPubMed Google Scholar - Hiroki Tsutsui
You can also search for this author inPubMed Google Scholar - Keiko Shiina
You can also search for this author inPubMed Google Scholar - Stefanie Sprunck
You can also search for this author inPubMed Google Scholar - Hidenori Takeuchi
You can also search for this author inPubMed Google Scholar - Ryoko Yui
You can also search for this author inPubMed Google Scholar - Ryushiro D. Kasahara
You can also search for this author inPubMed Google Scholar - Yuki Hamamura
You can also search for this author inPubMed Google Scholar - Akane Mizukami
You can also search for this author inPubMed Google Scholar - Daichi Susaki
You can also search for this author inPubMed Google Scholar - Nao Kawano
You can also search for this author inPubMed Google Scholar - Takashi Sakakibara
You can also search for this author inPubMed Google Scholar - Shoko Namiki
You can also search for this author inPubMed Google Scholar - Kie Itoh
You can also search for this author inPubMed Google Scholar - Kurataka Otsuka
You can also search for this author inPubMed Google Scholar - Motomichi Matsuzaki
You can also search for this author inPubMed Google Scholar - Hisayoshi Nozaki
You can also search for this author inPubMed Google Scholar - Tsuneyoshi Kuroiwa
You can also search for this author inPubMed Google Scholar - Akihiko Nakano
You can also search for this author inPubMed Google Scholar - Masahiro M. Kanaoka
You can also search for this author inPubMed Google Scholar - Thomas Dresselhaus
You can also search for this author inPubMed Google Scholar - Narie Sasaki
You can also search for this author inPubMed Google Scholar - Tetsuya Higashiyama
You can also search for this author inPubMed Google Scholar
Corresponding author
Correspondence toTetsuya Higashiyama.
Supplementary information
Supplementary Information
This file contains Supplementary Figures 1-3 with Legends, Supplementary Tables 1-4 and the Legend for Supplementary Movie 1. (PDF 6881 kb)
Supplementary Movie 1
This movie file shows in vitro attraction assay using a pipette (see file s1 for full legend). (AVI 26776 kb)
PowerPoint slides
Rights and permissions
About this article
Cite this article
Okuda, S., Tsutsui, H., Shiina, K. et al. Defensin-like polypeptide LUREs are pollen tube attractants secreted from synergid cells.Nature 458, 357–361 (2009). https://doi.org/10.1038/nature07882
- Received: 28 October 2008
- Accepted: 10 February 2009
- Issue Date: 19 March 2009
- DOI: https://doi.org/10.1038/nature07882
This article is cited by
Editorial Summary
Floral attraction: elusive pollen-tube attractant identified
Precise pollen tube guidance is critical for the successful fertilization of flowering plants. The concept of a pollen tube attractant was proposed in the late nineteenth century when pollen tubes were found to grow towards excised pistil tissues on medium. In 2001 the synergid cells, situated next to the egg, were shown to secrete a soluble factor that guides the growing pollen tube towards the embryo sac. Now at long last, these pollen tube attractants have been identified. Synergid cells were isolated from Torenia fournieri ('wishbone flower') plants, which are unique in having a protruding embryo sac. The secreted guidance factors were identified as cysteine-rich polypeptides belonging to the sub group of defensin-like proteins, and named LUREs.