KAI2- and MAX2-mediated responses to karrikins and strigolactones are largely independent of HY5 in arabidopsis seedlings

Molecular Plant

Volumn 6, Issue 1, 2013, Pages 63-75

  Waters, Mark T ^a   Smith, Steven M ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS;

3-METHYL-2H-FURO(2,3-C)PYRAN-2-ONE; ARABIDOPSIS PROTEIN; BASIC LEUCINE ZIPPER TRANSCRIPTION FACTOR; CARRIER PROTEIN; FURAN DERIVATIVE; GR24 COMPOUND; HTL PROTEIN, ARABIDOPSIS; HY5 PROTEIN, ARABIDOPSIS; HYDROLASE; LACTONE; MAX2 PROTEIN, ARABIDOPSIS; MESSENGER RNA; NUCLEAR PROTEIN; PYRAN DERIVATIVE;

ARABIDOPSIS; BIOLOGICAL MODEL; DRUG EFFECTS; GENE EXPRESSION REGULATION; GENETIC COMPLEMENTATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; LIGHT; METABOLISM; PHENOTYPE; PLANT GROWTH; RADIATION RESPONSE; SEEDLING;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; BASIC-LEUCINE ZIPPER TRANSCRIPTION FACTORS; CARRIER PROTEINS; FURANS; GENE EXPRESSION REGULATION, PLANT; GENETIC COMPLEMENTATION TEST; HYDROLASES; HYPOCOTYL; LACTONES; LIGHT; MODELS, BIOLOGICAL; NUCLEAR PROTEINS; PHENOTYPE; PYRANS; RNA, MESSENGER; SEEDLING;

EID: 84875721293     PISSN: 16742052     EISSN: 17529867     Source Type: Journal    
DOI: 10.1093/mp/sss127     Document Type: Article

References (55)

1. Agusti, J., Herold, S., Schwarz, M., Sanchez, P., Ljung, K., Dun, E.A., Brewer, P.B., Beveridge, C.A., Sieberer, T., Sehr, E.M., et al. (2011). Strigolactone signaling is required for auxin-dependent stimulation of secondary growth in plants. Proc. Natl. Acad. Sci. U. S. A. 108, 20242-20247.
2. Ang, L.H., Chattopadhyay, S., Wei, N., Oyama, T., Okada, K., Batschauer, A., and Deng, X.W. (1998). Molecular interaction between COP1 and HY5 defines a regulatory switch for light control of Arabidopsis development. Mol. Cell 1, 213-222.
3. Arite, T., Iwata, H., Ohshima, K., Maekawa, M., Nakajima, M., Kojima, M., Sakakibara, H., and Kyozuka, J. (2007). DWARF10, an RMS1/MAX4/DAD1 ortholog, controls lateral bud outgrowth in rice. Plant J. 51, 1019-1029.
4. Bauer, D., Viczián, A., Kircher, S., Nobis, T., Nitschke, R., Kunkel, T., Panigrahi, K.C.S., Adám, E., Fejes, E., Schäfer, E., et al. (2004). Constitutive photomorphogenesis 1 and multiple photoreceptors control degradation of phytochrome interacting factor 3, a transcription factor required for light signaling in Arabidopsis. Plant Cell 16, 1433-1445.
5. Bennett, T., Sieberer, T., Willett, B., Booker, J., Luschnig, C., and Leyser, O. (2006). The Arabidopsis MAX pathway controls shoot branching by regulating auxin transport. Curr. Biol. 16, 553-563.
6. Boerjan, W., Cervera, M.T., Delarue, M., Beeckman, T., Dewitte, W., Bellini, C., Caboche, M., Van Onckelen, H., Van Montagu, M., and Inzé, D. (1995). Superroot, a recessive mutation in Arabidopsis, confers auxin overproduction. Plant Cell 7, 1405-1419.
7. Chattopadhyay, S., Ang, L.H., Puente, P., Deng, X.W., and Wei, N. (1998). Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression. Plant Cell 10, 673-683.
8. Chaves, I., Pokorny, R., Byrdin, M., Hoang, N., Ritz, T., Brettel, K., Essen, L.-O., van der Horst, G.T.J., Batschauer, A., and Ahmad, M. (2011). The cryptochromes: blue light photoreceptors in plants and animals. Annu. Rev. Plant Biol. 62, 335-364.
9. Chen, M., and Chory, J. (2011). Phytochrome signaling mechanisms and the control of plant development. Trends Cell Biol. 21, 664-671.
10. Cluis, C.P., Mouchel, C.F., and Hardtke, C.S. (2004). The Arabidopsis transcription factor HY5 integrates light and hormone signaling pathways. Plant J. 38, 332-347.
11. Cook, C.E., Whichard, L.P., Turner, B., Wall, M.E., and Egley, G.H. (1966). Germination of witchweed (Striga lutea Lour.): Isolation and properties of a potent stimulant. Science 154, 1189-1190.
12. Crawford, S., Shinohara, N., Sieberer, T., Williamson, L., George, G., Hepworth, J., Müller, D., Domagalska, M.A., and Leyser, O. (2010). Strigolactones enhance competition between shoot branches by dampening auxin transport. Development 137, 2905-2913.
13. Curtis, M.D., and Grossniklaus, U. (2003). A Gateway cloning vector set for high-throughput functional analysis of genes in planta. Plant Physiol. 133, 462-469.
14. Deng, X., and Quail, P. (1992). Genetic and phenotypic characterization of cop1 mutants of Arabidopsis thaliana. Plant J. 2, 83-95.
15. Flematti, G.R., Ghisalberti, E.L., Dixon, K.W., and Trengove, R.D. (2004). A compound from smoke that promotes seed germination. Science 305, 977.
16. Flematti, G.R., Ghisalberti, E.L., Dixon, K.W., and Trengove, R.D. (2009). Identification of alkyl substituted 2H-furo[2, 3- c]pyran- 2-ones as germination stimulants present in smoke. J. Agric. Food Chem. 57, 9475-9480.
17. Foo, E., Bullier, E., Goussot, M., Foucher, F., Rameau, C., and Beveridge, C.A. (2005). The branching gene RAMOSUS1 mediates interactions among two novel signals and auxin in pea. Plant Cell 17, 464-474.
18. Gomez-Roldan, V., Fermas, S., Brewer, P.B., Puech-Pagès, V., Dun, E.A., Pillot, J.-P., Letisse, F., Matusova, R., Danoun, S., Portais, J.-C., et al. (2008). Strigolactone inhibition of shoot branching. Nature 455, 189-194.
19. Hayward, A., Stirnberg, P., Beveridge, C., and Leyser, O. (2009). Interactions between auxin and strigolactone in shoot branching control. Plant Physiol. 151, 400-412.
20. Kapulnik, Y., Delaux, P.-M., Resnick, N., Mayzlish-Gati, E., Wininger, S., Bhattacharya, C., Séjalon-Delmas, N., Combier, J.-P., Bécard, G., Belausov, E., et al. (2011). Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis. Planta 233, 209-216.
21. Koltai, H. (2011). Strigolactones are regulators of root development. New Phytol. 190, 545-549.
22. Koornneef, M., Rolff, E., and Spruit, C. (1980). Genetic control of light-inhibited hypocotyl elongation in Arabidopsis thaliana (L.) Heynh. Z Pflanzenphysiol 100, 147-160.
23. Lee, J., He, K., Stolc, V., Lee, H., Figueroa, P., Gao, Y., Tongprasit, W., Zhao, H., Lee, I., and Deng, X.W. (2007). Analysis of transcription factor HY5 genomic binding sites revealed its hierarchical role in light regulation of development. Plant Cell 19, 731-749.
24. Leivar, P., Monte, E., Oka, Y., Liu, T., Carle, C., Castillon, A., Huq, E., and Quail, P.H. (2008). Multiple phytochrome-interacting bHLH transcription factors repress premature seedling photomorphogenesis in darkness. Curr. Biol. 18, 1815-1823.
25. Light, M., Daws, M., and van Staden, J. (2009). Smoke-derived butenolide: towards understanding its biological effects. S. Afr. J. Bot. 75, 1-7.
26. Liu, B., Zuo, Z., Liu, H., Liu, X., and Lin, C. (2011). Arabidopsis cryptochrome 1 interacts with SPA1 to suppress COP1 activity in response to blue light. Genes Dev. 25, 1029-1034.
27. Long, R.L., Stevens, J.C., Griffiths, E.M., Adamek, M., Gorecki, M.J., Powles, S.B., and Merritt, D.J. (2011). Seeds of Brassicaceae weeds have an inherent or inducible response to the germination stimulant karrikinolide. Ann. Bot. 108, 933-944.
28. Long, R.L., Williams, K., Griffiths, E.M., Flematti, G.R., Merritt, D.J., Stevens, J.C., Turner, S.R., Powles, S.B., and Dixon, K.W. (2010). Prior hydration of Brassica tournefortii seeds reduces the stimulatory effect of karrikinolide on germination and increases seed sensitivity to abscisic acid. Ann. Bot. 105, 1063-1070.
29. Nelson, D.C., Flematti, G.R., Ghisalberti, E.L., Dixon, K.W., and Smith, S.M. (2012). Regulation of seed germination and seedling growth by chemical signals from burning vegetation. Annu. Rev. Plant Biol. 63, 107-130.
30. Nelson, D.C., Flematti, G.R., Riseborough, J.-A., Ghisalberti, E.L., Dixon, K.W., and Smith, S.M. (2010). Karrikins enhance light responses during germination and seedling development in Arabidopsis thaliana. Proc. Natl. Acad. Sci. USA 107, 7095-7100.
31. Nelson, D.C., Riseborough, J.-A., Flematti, G.R., Stevens, J., Ghisalberti, E.L., Dixon, K.W., and Smith, S.M. (2009). Karrikins discovered in smoke trigger Arabidopsis seed germination by a mechanism requiring gibberellic acid synthesis and light. Plant Physiol. 149, 863-873.
32. Nelson, D.C., Scaffidi, A., Dun, E.A., Waters, M.T., Flematti, G.R., Dixon, K.W., Beveridge, C.A., Ghisalberti, E.L., and Smith, S.M. (2011). F-box protein MAX2 has dual roles in karrikin and strigolactone signaling in Arabidopsis thaliana. Proc. Natl. Acad. Sci. USA 108, 8897-8902.
33. Osterlund, M.T., Hardtke, C.S., Wei, N., and Deng, X.W. (2000). Targeted destabilization of HY5 during light-regulated development of Arabidopsis. Nature 405, 462-466.
34. Oyama, T., Shimura, Y., and Okada, K. (1997). The Arabidopsis HY5 gene encodes a bZIP protein that regulates stimulus-induced development of root and hypocotyl. Genes Dev. 11, 2983-2995.
35. Park, J.-Y., Kim, H.-J., and Kim, J. (2002). Mutation in domain II of IAA1 confers diverse auxin-related phenotypes and represses auxin-activated expression of Aux/IAA genes in steroid regulator- inducible system. Plant J. 32, 669-683.
36. Quail, P.H. (2010). Phytochromes. Curr. Biol. 20, R504-507.
37. Rasmussen, A., Mason, M., De Cuyper, C., Brewer, P.B., Herold, S., Agusti, J., Geelen, D.N.V., Greb, T., Goormachtig, S., Beeckman, T., et al. (2012). Strigolactones suppress adventitious rooting in Arabidopsis and pea. Plant Physiol. 158, 1976-1987.
38. Ruyter-Spira, C., Kohlen, W., Charnikhova, T., van Zeijl, A., van Bezouwen, L., de Ruijter, N., Cardoso, C., Lopez-Raez, J.A., Matusova, R., Bours, R., et al. (2011). Physiological effects of the synthetic strigolactone analog GR24 on root system architecture in Arabidopsis: another belowground role for strigolactones? Plant Physiol. 155, 721-734.
39. Seo, H.S., Yang, J.-Y., Ishikawa, M., Bolle, C., Ballesteros, M.L., and Chua, N.-H. (2003). LAF1 ubiquitination by COP1 controls photomorphogenesis and is stimulated by SPA1. Nature 423, 995-999.
40. Shen, H., Luong, P., and Huq, E. (2007). The F-box protein MAX2 functions as a positive regulator of photomorphogenesis in Arabidopsis. Plant Physiol. 145, 1471-1483.
41. Shen, H., Zhu, L., Bu, Q.-Y., and Huq, E. (2012). MAX2 Affects Multiple Hormones to Promote Photomorphogenesis. Mol. Plant 5, 224-236.
42. Shen, H., Zhu, L., Castillon, A., Majee, M., Downie, B., and Huq, E. (2008). Light-induced phosphorylation and degradation of the negative regulator phytochrome-interacting factor1 from Arabidopsis depend upon its direct physical interactions with photoactivated phytochromes. Plant Cell 20, 1586-1602.
43. Shin, J., Kim, K., Kang, H., Zulfugarov, I.S., Bae, G., Lee, C.-H., Lee, D., and Choi, G. (2009). Phytochromes promote seedling light responses by inhibiting four negatively-acting phytochromeinteracting factors. Proc. Natl. Acad. Sci. USA 106, 7660-7665.
44. Sibout, R., Sukumar, P., Hettiarachchi, C., Holm, M., Muday, G.K., and Hardtke, C.S. (2006). Opposite Root Growth Phenotypes of hy5 versus hy5 hyh Mutants Correlate with Increased Constitutive Auxin Signaling. PLoS Genetics 2, e202.
45. Stephenson, P.G., Fankhauser, C., and Terry, M.J. (2009). PIF3 is a repressor of chloroplast development. Proc. Natl. Acad. Sci. USA 106, 7654-7659.
46. Sun, X.-D., and Ni, M. (2011). Hyposensitive to light, an alpha/beta fold protein, acts downstream of elongated hypocotyl 5 to regulate seedling deetiolation. Mol. Plant 4, 116-126.
47. Tsuchiya, Y., Vidaurre, D., Toh, S., Hanada, A., Nambara, E., Kamiya, Y., Yamaguchi, S., and McCourt, P. (2010). A small-molecule screen identifies new functions for the plant hormone strigolactone. Nat. Chem. Biol. 6, 741-749.
48. Umehara, M., Hanada, A., Yoshida, S., Akiyama, K., Arite, T., Takeda-Kamiya, N., Magome, H., Kamiya, Y., Shirasu, K., Yoneyama, K., et al. (2008). Inhibition of shoot branching by new terpenoid plant hormones. Nature 455, 195-200.
49. Van Buskirk, E.K., Decker, P.V., and Chen, M. (2012). Photobodies in light signaling. Plant Physiol. 158, 52-60.
50. Waters, M.T., Nelson, D.C., Scaffidi, A., Flematti, G.R., Sun, Y., Dixon, K.W., and Smith, S.M. (2012). Specialization within the DWARF14 protein family confers distinct responses to karrikins and strigolactones in Arabidopsis. Development 139, 1285-1295.
51. Winkel-Shirley, B. (2002). Biosynthesis of flavonoids and effects of stress. Curr. Opin. Plant Biol. 5, 218-223.
52. Xie, X., Yoneyama, K., and Yoneyama, K. (2010). The strigolactone story. Annu. Rev. Phytopathol. 48, 93-117.
53. Yang, H., Tang, R., and Cashmore, A. (2001). The signaling mechanism of Arabidopsis CRY1 involves direct interaction with COP1. Plant Cell 13, 2573.
54. Yang, X., Lee, S., So, J.-H., Dharmasiri, S., Dharmasiri, N., Ge, L., Jensen, C., Hangarter, R., Hobbie, L., and Estelle, M. (2004). The IAA1 protein is encoded by AXR5 and is a substrate of SCF(TIR1). Plant J. 40, 772-782.
55. Zhao, Y., Christensen, S.K., Fankhauser, C., Cashman, J.R., Cohen, J.D., Weigel, D., and Chory, J. (2001). A role for flavin monooxygenase- like enzymes in auxin biosynthesis. Science 291, 306-309.