The jasmonate-responsive GTR1 transporter is required for gibberellin-mediated stamen development in Arabidopsis

Nature Communications

Volumn 6, Issue , 2015, Pages

  Saito, Hikaru ^a   Oikawa, Takaya ^b   Hamamoto, Shin ^b   Ishimaru, Yasuhiro ^b   Kanamori Sato, Miyu ^a   Sasaki Sekimoto, Yuko ^a   Utsumi, Tomoya ^a   Chen, Jing ^a   Kanno, Yuri ^c   Masuda, Shinji ^a   Kamiya, Yuji ^c   Seo, Mitsunori ^c   Uozumi, Nobuyuki ^b   Ueda, Minoru ^b   Ohta, Hiroyuki ^a  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^b TOHOKU UNIVERSITY   (Japan)

^c RIKEN Plant Science Center   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; GIBBERELLIN; GLUCOSINOLATE; GLUCOSINOLATE TRANSPORTER GTR1; JASMONIC ACID; PHYTOHORMONE; UNCLASSIFIED DRUG; ARABIDOPSIS PROTEIN; CYCLOPENTANE DERIVATIVE; GLUCOSE TRANSPORTER; GTR1 PROTEIN, ARABIDOPSIS; OXYLIPIN;

ABSCISIC ACID; CELLS AND CELL COMPONENTS; DIFFUSION; GENE EXPRESSION; HETEROGENEITY; HORMONE; MEMBRANE; MUTATION; PHENOTYPE; PROTEIN;

ARABIDOPSIS THALIANA; ARTICLE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; FLOWER DEVELOPMENT; GENE MUTATION; HISTOCHEMISTRY; HORMONE TRANSPORT; IN VITRO STUDY; NONHUMAN; PHENOTYPE; PLANT GENE; PLANT GROWTH; PLANT INFERTILITY; POLLEN GERMINATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; QUANTITATIVE ANALYSIS; REGULATORY MECHANISM; SIGNAL TRANSDUCTION; STAMEN FILAMENT; ARABIDOPSIS; FLOWER; GENE EXPRESSION REGULATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; PHYSIOLOGY;

ARABIDOPSIS; ARABIDOPSIS THALIANA;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; CYCLOPENTANES; FLOWERS; GENE EXPRESSION REGULATION, PLANT; GIBBERELLINS; MONOSACCHARIDE TRANSPORT PROTEINS; OXYLIPINS;

EID: 84929110780     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms7095     Document Type: Article

References (53)

1. Petrásek, J. & Friml, J. Auxin transport routes in plant development. Development 136, 2675-2688 (2009).
2. Léran, S. et al. A unified nomenclature of NITRATE TRANSPORTER 1/PEPTIDE TRANSPORTER family members in plants. Trends Plant Sci. 19, 5-9 (2013).
3. Krouk, G. et al. Nitrate-regulated auxin transport by NRT1. 1 defines a mechanism for nutrient sensing in plants. Dev. Cell 18, 927-937 (2010).
4. Kang, J. et al. PDR-type ABC transporter mediates cellular uptake of the phytohormone abscisic acid. Proc. Natl Acad. Sci. USA 107, 2355-2360 (2010).
5. Kuromori, T. et al. ABC transporter AtABCG25 is involved in abscisic acid transport and responses. Proc. Natl Acad. Sci. USA 107, 2361-2366 (2010).
6. Kanno, Y. et al. Identification of an abscisic acid transporter by functional screening using the receptor complex as a sensor. Proc. Natl Acad. Sci. USA 109, 9653-9658 (2012).
7. Zhang, H. et al. A DTX/MATE-type transporter facilitates abscisic acid efflux and modulates ABA sensitivity and drought tolerance in Arabidopsis. Mol. Plant 7, 1522-1532 (2014).
8. Ko, D. et al. Arabidopsis ABCG14 is essential for the root-to-shoot translocation of cytokinin. Proc. Natl Acad. Sci. USA 111, 7150-7155 (2014).
9. Zhang, K. et al. Arabidopsis ABCG14 protein controls the acropetal translocation of root-synthesized cytokinins. Nat. Commun. 5, 3274 (2014).
10. Kretzschmar, T. et al. A petunia ABC protein controls strigolactone-dependent symbiotic signalling and branching. Nature 483, 341-344 (2012).
11. Peng, J. Gibberellin and jasmonate crosstalk during stamen development. J. Int. Plant Biol. 51, 1064-1070 (2009).
12. Sun, T. P. Gibberellin-GID1-DELLA: a pivotal regulatory module for plant growth and development. Plant Physiol. 154, 567-570 (2010).
13. Swain, S. M. & Singh, D. P. Tall tales from sly dwarves: novel functions of gibberellins in plant development. Trends Plant Sci. 10, 123-129 (2005).
14. Acosta, I. F. & Farmer, E. E. in The Arabidopsis book (eds Somerville, C. R. & Meyerowitz, E. M.) (American Society of Plant Biologists, 2010).
15. Wasternack, C., Forner, S., Strnad, M. & Hause, B. Jasmonates in flower and seed development. Biochimie. 95, 79-85 (2013).
16. Schilmiller, A. L. & Howe, G. A. Systemic signaling in the wound response. Curr. Opin. Plant Biol. 8, 369-377 (2005).
17. Browse, J. Jasmonate passes muster: a receptor and targets for the defense hormone. Annu. Rev. Plant Biol. 60, 183-205 (2009).
18. Thines, B., Mandaokar, A. & Browse, J. Characterizing jasmonate regulation of male fertility in Arabidopsis. Methods Mol. Biol. 1011, 13-23 (2013).
19. Koornneef, M. & Van Der Veen, J. H. Induction and analysis of gibberellin sensitive mutants in Arabidopsis thaliana (L.) Heynh. Theor. Appl. Genet. 58, 257-263 (1980).
20. Sun, T. P., Goodman, H. M. & Ausubel, F. M. Cloning the Arabidopsis GA1 locus by genomic subtraction. Plant Cell 4, 119-128 (1992).
21. Sun, T. P. in The Arabidopsis Book (eds Somerville, C. R. & Meyerowitz, E. M.) (American Society of Plant Biologists, 2008).
22. Cheng, H. et al. Gibberellin regulates Arabidopsis floral development via suppression of DELLA protein function. Development 131, 1055-1064 (2004).
23. Hou, X., Lee, L. Y., Xia, K., Yan, Y. & Yu, H. DELLAs modulate jasmonate signaling via competitive binding to JAZs. Dev. Cell 19, 884-894 (2010).
24. Hong, G. J., Xue, X. Y., Mao, Y. B., Wang, L. J. & Chen, X. Y. Arabidopsis MYC2 interacts with DELLA proteins in regulating sesquiterpene synthase gene expression. Plant Cell 24, 2635-2648 (2012).
25. Yang, D. et al. Plant hormone jasmonate prioritizes defense over growth by interfering with gibberellin signaling cascade. Proc. Natl Acad. Sci. USA 109, E1192-E1200 (2012).
26. Sasaki-Sekimoto, Y. et al. Basic helix-loop-helix transcription factors JASMONATE-ASSOCIATED MYC2-LIKE1 (JAM1), JAM2, and JAM3 are negative regulators of jasmonate responses in Arabidopsis. Plant Physiol. 163, 291-304 (2013).
27. Obayashi, T., Nishida, K., Kasahara, K. & Kinoshita, K. ATTED-II updates: condition-specific gene coexpression to extend coexpression analyses and applications to a broad range of flowering plants. Plant Cell Physiol. 52, 213-219 (2011).
28. Obayashi, T. & Kinoshita, K. Rank of correlation coefficient as a comparable measure for biological significance of gene coexpression. DNA Res. 16, 249-260 (2009).
29. Nour-Eldin, H. H. et al. NRT/PTR transporters are essential for translocation of glucosinolate defence compounds to seeds. Nature 488, 531-534 (2012).
30. Lorenzo, O., Chico, J. M., Sánchez-Serrano, J. J. & Solano, R. JASMONATE-INSENSITIVE1 encodes a MYC transcription factor essential to discriminate between different jasmonate-regulated defense responses in Arabidopsis. Plant Cell 16, 1938-1950 (2004).
31. Thines, B. et al. JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling. Nature 448, 661-665 (2007).
32. Chini, A. et al. The JAZ family of repressors is the missing link in jasmonate signalling. Nature 448, 666-671 (2007).
33. Yan, Y. et al. A downstream mediator in the growth repression limb of the jasmonate pathway. Plant Cell 19, 2470-2483 (2007).
34. Weaver, L. M., Gan, S., Quirino, B. & Amasino, R. M. A comparison of the expression patterns of several senescence-associated genes in response to stress and hormone treatment. Plant Mol. Biol. 37, 455-469 (1998).
35. Smyth, D. R., Bowman, J. L. & Meyerowitz, E. M. Early flower development in Arabidopsis. Plant Cell 2, 755-767 (1990).
36. Plackett, A. R., Thomas, S. G., Wilson, Z. A. & Hedden, P. Gibberellin control of stamen development: a fertile field. Trends Plant Sci. 16, 568-578 (2011).
37. Liu, K. H. & Tsay, Y. F. Switching between the two action modes of the dual-affinity nitrate transporter CHL1 by phosphorylation. EMBO J. 22, 1005-1013 (2003).
38. Hirano, K. et al. Comprehensive transcriptome analysis of phytohormone biosynthesis and signaling genes in microspore/pollen and tapetum of rice. Plant Cell Physiol. 49, 1429-1450 (2008).
39. Kanno, Y. et al. Comprehensive hormone profiling in developing Arabidopsis seeds: examination of the site of ABA biosynthesis, ABA transport and hormone interactions. Plant Cell Physiol. 51, 1988-2001 (2010).
40. Yamaguchi, S. Gibberellin metabolism and its regulation. Annu. Rev. Plant Biol. 59, 225-251 (2008).
41. Czechowski, T., Stitt, M., Altmann, T., Udvardi, M. K. & Scheible, W. R. Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis. Plant Physiol. 139, 5-17 (2005).
42. Nakagawa, T. et al. Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation. J. Biosci. Bioeng. 104, 31-41 (2007).
43. Berberich, T., Takahashi, Y., Saitoh, H. & Terauchi, R. in The Handbook of Plant Functional Genomics (eds Kahl, G. & Meksem, K.) Ch. 6, 113-136 (Wiley, 2008).
44. Kiyota, H., Higashi, E., Koike, T. & Oritani, T. Lipase-catalyzed preparation of both enantiomers of methyl jasmonate. Tetrahedron Asymmetry 12, 1035-1038 (2001).
45. Asamitsu, Y., Nakamura, Y., Ueda, M., Kuwahara, S. & Kiyota, H. Synthesis and odor description of both enantiomers of methyl 4,5-didehydro-jasmonate, a component of jasmin absolute. Chem. Biodivers. 3, 654-659 (2006).
46. Nakamura, Y., Miyatake, R., Inomata, S. & Ueda, M. Synthesis and bioactivity of potassium β-D-glucopyranosyl 12-hydroxy jasmonate and related compounds. Biosci. Biotechnol. Biochem. 72, 2867-2876 (2008).
47. Kramell, R., Schmidt, J., Schneider, G., Sembdner, G. & Schreiber, K. Synthesis of N-(jasmonoyl)amino acid conjugates. Tetrahedron 44, 5791-5807 (1988).
48. Abramoff, M. D., Magelhaes, P. J. & Ram, S. J. Image processing with ImageJ. Biophotonics Int. 11, 36-42 (2004).
49. Jefferson, R. A., Kavanagh, T. A. & Bevan, M. W. GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 20, 3901-3907 (1987).
50. Adachi, S., Nobusawa, T. & Umeda, M. Quantitative and cell type-specific transcriptional regulation of A-type cyclin-dependent kinase in Arabidopsis thaliana. Dev. Biol. 329, 306-314 (2009).
51. + uptake in Saccharomyces cerevisiae. Plant Physiol. 122, 1249-1259 (2000).
52. Fan, L. M., Wang, Y. F., Wang, H. & Wu, W. H. In vitro Arabidopsis pollen germination and characterization of the inward potassium currents in Arabidopsis pollen grain protoplasts. J. Exp. Bot. 52, 1603-1614 (2001).
53. Yamaguchi, N. et al. Gibberellin acts positively then negatively to control onset of flower formation in Arabidopsis. Science 344, 638-641 (2014).