Chemical control of xylem differentiation by thermospermine, xylemin, and auxin

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Yoshimoto, Kaori ^a   Takamura, Hiroyoshi ^a   Kadota, Isao ^a   Motose, Hiroyasu ^a   Takahashi, Taku ^a  

^a OKAYAMA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

2,4 DICHLOROPHENOXYACETIC ACID; 2,4-DICHLOROPHENOXYACETIC ACID ISOOCTYL ESTER; ARABIDOPSIS PROTEIN; INDOLEACETIC ACID DERIVATIVE; PUTRESCINE; SPERMIDINE; SPERMINE; THERMOSPERMINE; XYLEMIN;

ANALOGS AND DERIVATIVES; ANTAGONISTS AND INHIBITORS; ARABIDOPSIS; BIOSYNTHESIS; CELL DIFFERENTIATION; DRUG EFFECTS; METABOLISM; PHYSIOLOGY; XYLEM;

2,4-DICHLOROPHENOXYACETIC ACID; ARABIDOPSIS; ARABIDOPSIS PROTEINS; CELL DIFFERENTIATION; INDOLEACETIC ACIDS; PUTRESCINE; SPERMIDINE; SPERMINE; XYLEM;

EID: 84958568920     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep21487     Document Type: Article

References (46)

1. Igarashi, K., Kashiwagi, K. Modulation of cellular function by polyamines. Int. J. Biochem. Cell Biol. 42, 39-51 (2010).
2. Pegg, A. E., Casero, R. A. Current status of the polyamine research field. Methods Mol. Biol. 720, 3-35 (2011).
3. Fuell, C., Elliott, K. A., Hanfrey, C. C., Franceschetti, M., Michael, A. J. Polyamine biosynthetic diversity in plants and algae. Plant Physiol. Biochem. 48, 513-520 (2010).
4. Bagni, N., Tassoni, A. Biosynthesis, oxidation and conjugation of aliphatic polyamines in higher plants. Amino Acids 20, 301-317 (2001).
5. Kusano, T., Berberich, T., Tateda, C., Takahashi, Y. Polyamines: essential factors for growth and survival. Planta 228, 367-381 (2008).
6. Takahashi, T., Kakehi, J. Polyamines: ubiquitous polycations with unique roles in growth and stress responses. Ann. Bot. 105, 1-6 (2009).
7. Moschou, P. N. et al. The polyamines and their catabolic products are significant players in the turnover of nitrogenous molecules in plants. J. Exp. Bot. 63, 5003-5015 (2012).
8. Tiburcio, A. F., Altabella, T., Bitrian, M., Alcazar, R. The roles of polyamines during the lifespan of plants: from development to stress. Planta 240, 1-18 (2014).
9. Oshima, T. A new polyamine, thermospermine, 1,12-diamino-4,8-diazadodecane, from an extreme thermophile. J Biol. Chem. 254, 8720-8722 (1979).
10. Minguet, E. G., Vera-Sirera, F., Marina, A., Carbonell, J., Blázquez, M. A. Evolutionary diversification in polyamine biosynthesis. Mol Biol Evol. 25, 2119-2128 (2008).
11. Takano, A., Kakehi, J., Takahashi, T. Thermospermine is not a minor polyamine in the plant kingdom. Plant Cell Physiol. 53, 606-616 (2012).
12. Knott, J. M., Römer, P., Sumper, M. Putative spermine synthases from Thalassiosira pseudonana and Arabidopsis thaliana synthesize thermospermine rather than spermine. FEBS Lett. 581, 3081-3086 (2007).
13. Kakehi, J., Kuwashiro, Y., Niitsu, M., Takahashi, T. Thermospermine is required for stem elongation in Arabidopsis thaliana. Plant Cell Physiol. 49, 1342-1349 (2008).
14. Hanzawa, Y., Takahashi, T., Komeda, Y. ACL5: an Arabidopsis gene required for internodal elongation after flowering. Plant J. 12, 863-874 (1997).
15. Hanzawa, Y. et al. ACAULIS5, an Arabidopsis gene required for stem elongation, encodes a spermine synthase. EMBO J. 19, 4248-4256 (2000).
16. Imai, A. et al. Spermine is not essential for survival of Arabidopsis. FEBS Lett. 556, 148-152 (2004).
17. Yoshimoto, K. et al. A chemical biology approach reveals an opposite action between thermospermine and auxin in xylem development in Arabidopsis thaliana. Plant Cell Physiol. 53, 635-645 (2012).
18. Yoshimoto, K. et al. Thermospermine suppresses auxin-inducible xylem differentiation in Arabidopsis thaliana. Plant Signal Behav. 7, 937-939 (2012).
19. Tong, W. et al. Thermospermine modulates expression of auxin-related genes in Arabidopsis. Front Plant Sci. 5, 94 (2014).
20. Baima, S. et al. Negative feedback regulation of auxin signaling by ATHB8/ACL5-BUD2 transcription module. Mol. Plant 7, 1006-1025 (2014).
21. Milhinhos, A. et al. Thermospermine levels are controlled by an auxin-dependent feedback loop mechanism in Populus xylem. Plant J. 75, 685-698 (2013).
22. Carlsbecker, A. et al. Cell signalling by microRNA165/6 directs gene dose-dependent root cell fate. Nature 465, 316-321 (2010).
23. Donner, T., Sherr, I., Scarpella, E. Regulation of preprocambial cell state acquisition by auxin signaling in Arabidopsis leaves. Development 136, 3235-3246 (2009).
24. Kan, T., Fukuyama, T. Ns strategies: a highly versatile synthetic method for amines. Chem. Commun. 21, 353-359 (2004).
25. Przemeck, G. K., Mattsson, J., Hardtke, C. S., Sung, Z. R., Berleth, T. Studies on the role of the Arabidopsis gene MONOPTEROS in vascular development and plant cell axialization. Planta 200, 229-237 (1996).
26. Hardtke, C. S., Berleth, T. The Arabidopsis gene MONOPTEROS encodes a transcription factor mediating embryo axis formation and vascular development. EMBO J. 17, 1405-1411 (1998).
27. Imai, A. et al. The dwarf phenotype of the Arabidopsis acl5 mutant is suppressed by a mutation in an upstream ORF of a bHLH gene. Development 133, 3575-3585 (2006).
28. Kakehi, J. et al. Mutations in ribosomal proteins, RPL4 and RACK1, suppress the phenotype of a thermospermine-deficient mutant of Arabidopsis thaliana. PLoS One 10, e0117309 (2015).
29. Fukuda, H., Komamine, A. Establishment of an experimental system for the study of tracheary element differentiation from single cells isolated from the mesophyll of Zinnia elegans. Plant Physiol. 65, 57-60 (1980).
30. De Rybel, B. et al. A bHLH complex controls embryonic vascular tissue establishment and indeterminate growth in Arabidopsis. Dev. Cell 24, 426-437 (2013).
31. Vera-Sirera, F. et al. A bHLH-based feedback loop restricts vascular cell proliferation in plants. Dev. Cell 35, 432-443 (2015).
32. Katayama, H. et al. A negative feedback loop controlling bHLH complexes is involved in vascular cell division and differentiation in the root apical meristem. Curr. Biol 25, 3144-3150 (2015).
33. Ohashi-Ito, K., Oguchi, M., Kojima, M., Sakakibara, H., Fukuda, H. Auxin-associated initiation of vascular cell differentiation by LONESOME HIGHWAY. Development 140, 765-769 (2013).
34. Sachs, T. Cell polarity and tissue patterning in plants. Development Suppl. 1, 83-93 (1991).
35. Scarpella, E., Marcos, D., Friml, J., Berleth, T. Control of leaf vascular patterning by polar auxin transport. Genes Dev. 20, 1015-1027 (2006).
36. Feugier, F. G., Iwasa, Y. How canalization can make loops: A new model of reticulated leaf vascular pattern formation. J. Theor. Biol. 243, 235-244 (2006).
37. Mähönen, A. P. et al. Cytokinin signaling and its inhibitor AHP6 regulate cell fate during vascular development. Science 311, 94-98 (2006).
38. Bishopp, A. et al. A mutually inhibitory interaction between auxin and cytokinin specifies vascular pattern in roots. Curr. Biol. 21, 917-926 (2011).
39. Hirakawa, Y., Kondo, Y., Fukuda, H. TDIF peptide signaling regulates vascular stem cell proliferation via the WOX4 homeobox gene in Arabidopsis. Plant Cell 22, 2618-2629 (2010).
40. Kondo, Y. et al. Plant GSK3 proteins regulate xylem cell differentiation downstream of TDIF-TDR signalling. Nat. Commun. 24, 3504 (2014).
41. Hayashi, K. et al. Auxin transport sites are visualized in planta using fluorescent auxin analogs. Proc Natl Acad Sci USA 111, 11557-11562 (2014).
42. Baima, S. et al. The expression of the Athb-8 homeobox gene is restricted to provascular cells in Arabidopsis thaliana. Development 121, 4171-4182 (1995).
43. Pyo, H., Demura, T., Fukuda, H. Spatial and temporal tracing of vessel differentiation in young Arabidopsis seedlings by the expression of an immature tracheary element-specific promoter. Plant Cell Physiol. 45, 1529-1536 (2004).
44. Takatani, S., Hirayama, T., Hashimoto, T., Takahashi, T., Motose, H. Abscisic acid induces ectopic outgrowth in epidermal cells through cortical microtubule reorganization in Arabidopsis thaliana. Sci Rep. 5, 11364 (2015).
45. Takahashi, T., Naito, S., Komeda, Y. Isolation and analysis of the expression of two genes for the 81-kilodalton heat-shock proteins from Arabidopsis. Plant Physiol. 99, 383-390 (1992).
46. Naka, Y. et al. Quantitative analysis of plant polyamines including thermospermine during growth and salinity stress. Plant Physiol Biochem. 48, 527-533 (2010).