Strigolactone/MAX2-Induced Degradation of Brassinosteroid Transcriptional Effector BES1 Regulates Shoot Branching

Developmental Cell

Volumn 27, Issue 6, 2013, Pages 681-688

  Wang, Yuan ^a   Sun, Shiyong ^a   Zhu, Wenjiao ^a   Jia, Kunpeng ^b   Yang, Hongquan ^b   Wang, Xuelu ^a  

^a FUDAN UNIVERSITY   (China)

^b SHANGHAI JIAO TONG UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

LACTONE DERIVATIVE; LIGASE; MAX2 PROTEIN; STRIGOLACTONE; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR BES1; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; GENE EXPRESSION; GENE SILENCING; IN VITRO STUDY; IN VIVO STUDY; NONHUMAN; PHENOTYPE; PLANT DEVELOPMENT; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN PROTEIN INTERACTION; ROSETTE FORMATION; SHOOT; SHOOT BRANCHING; SIGNAL TRANSDUCTION;

EID: 84890831797     PISSN: 15345807     EISSN: 18781551     Source Type: Journal    
DOI: 10.1016/j.devcel.2013.11.010     Document Type: Article

References (33)

1. Aguilar-Martínez J.A., Poza-Carrión C., Cubas P. Arabidopsis BRANCHED1 acts as an integrator of branching signals within axillary buds. Plant Cell 2007, 19:458-472.
2. Akiyama K., Matsuzaki K., Hayashi H. Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi. Nature 2005, 435:824-827.
3. Beveridge C.A., Kyozuka J. New genes in the strigolactone-related shoot branching pathway. Curr. Opin. Plant Biol. 2010, 13:34-39.
4. Booker J., Sieberer T., Wright W., Williamson L., Willett B., Stirnberg P., Turnbull C., Srinivasan M., Goddard P., Leyser O. MAX1 encodes a cytochrome P450 family member that acts downstream of MAX3/4 to produce a carotenoid-derived branch-inhibiting hormone. Dev. Cell 2005, 8:443-449.
5. Braun N., de Saint Germain A., Pillot J.P., Boutet-Mercey S., Dalmais M., Antoniadi I., Li X., Maia-Grondard A., Le Signor C., Bouteiller N., et al. The pea TCP transcription factor PsBRC1 acts downstream of Strigolactones to control shoot branching. Plant Physiol. 2012, 158:225-238.
6. Bythell-Douglas R.M., Waters M.T., Scaffidi A., Flematti G.R., Smith S.M., Bond C.S., Bond C.S. The structure of the karrikin-insensitive protein (KAI2) in Arabidopsis thaliana. PLoS ONE 2013, 8:e54758.
7. Cook C.E., Whichard L.P., Turner B., Wall M.E., Egley G.H. Germination of witchweed (Striga luteaLour.): isolation and properties of a potent stimulant. Science 1966, 154:1189-1190.
8. Crawford S., Shinohara N., Sieberer T., Williamson L., George G., Hepworth J., Müller D., Domagalska M.A., Leyser O. Strigolactones enhance competition between shoot branches by dampening auxin transport. Development 2010, 137:2905-2913.
9. Dixon K.W., Merritt D.J., Flematti G.R., Ghisalberti E.L. Karrikinolide-a phytoreactive compound derived from smoke with applications in horticulture, ecological restoration, and agriculture. Acta Hortic. 2009, 813:155-170.
10. Domagalska M.A., Leyser O. Signal integration in the control of shoot branching. Nat. Rev. Mol. Cell Biol. 2011, 12:211-221.
11. 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. Strigolactone inhibition of shoot branching. Nature 2008, 455:189-194.
12. Hamiaux C., Drummond R.S.M., Janssen B.J., Ledger S.E., Cooney J.M., Newcomb R.D., Snowden K.C. DAD2 is an α/β hydrolase likely to be involved in the perception of the plant branching hormone, strigolactone. Curr. Biol. 2012, 22:2032-2036.
13. Kagiyama M., Hirano Y., Mori T., Kim S.Y., Kyozuka J., Seto Y., Yamaguchi S., Hakoshima T. Structures of D14 and D14L in the strigolactone and karrikin signaling pathways. Genes Cells 2013, 18:147-160.
14. Mashiguchi K., Sasaki E., Shimada Y., Nagae M., Ueno K., Nakano T., Yoneyama K., Suzuki Y., Asami T. Feedback-regulation of strigolactone biosynthetic genes and strigolactone-regulated genes in Arabidopsis. Biosci. Biotechnol. Biochem. 2009, 73:2460-2465.
15. McGinnis K.M., Thomas S.G., Soule J.D., Strader L.C., Zale J.M., Sun T.P., Steber C.M. The Arabidopsis SLEEPY1 gene encodes a putative F-box subunit of an SCF E3 ubiquitin ligase. Plant Cell 2003, 15:1120-1130.
16. Murase K., Hirano Y., Sun T.P., Hakoshima T. Gibberellin-induced DELLA recognition by the gibberellin receptor GID1. Nature 2008, 456:459-463.
17. Nelson D.C., Scaffidi A., Dun E.A., Waters M.T., Flematti G.R., Dixon K.W., Beveridge C.A., Ghisalberti E.L., Smith S.M. F-box protein MAX2 has dual roles in karrikin and strigolactone signaling in Arabidopsis thaliana. Proc. Natl. Acad. Sci. USA 2011, 108:8897-8902.
18. Rechsteiner M., Rogers S.W. PEST sequences and regulation by proteolysis. Trends Biochem. Sci. 1996, 21:267-271.
19. Shinohara N., Taylor C., Leyser O. Strigolactone can promote or inhibit shoot branching by triggering rapid depletion of the auxin efflux protein PIN1 from the plasma membrane. PLOS Biol 2013, 11. 10.1371.
20. Stirnberg P., van De Sande K., Leyser H.M.O. MAX1 and MAX2 control shoot lateral branching in Arabidopsis. Development 2002, 129:1131-1141.
21. Stirnberg P., Furner I.J., Ottoline Leyser H.M. MAX2 participates in an SCF complex which acts locally at the node to suppress shoot branching. Plant J. 2007, 50:80-94.
22. Tsuchiya Y., Vidaurre D., Toh S., Hanada A., Nambara E., Kamiya Y., Yamaguchi S., McCourt P. A small-molecule screen identifies new functions for the plant hormone strigolactone. Nat. Chem. Biol. 2010, 6:741-749.
23. Ueguchi-Tanaka M., Ashikari M., Nakajima M., Itoh H., Katoh E., Kobayashi M., Chow T.Y., Hsing Y.I., Kitano H., Yamaguchi I., Matsuoka M. GIBBERELLIN INSENSITIVE DWARF1 encodes a soluble receptor for gibberellin. Nature 2005, 437:693-698.
24. Umehara M., Hanada A., Yoshida S., Akiyama K., Arite T., Takeda-Kamiya N., Magome H., Kamiya Y., Shirasu K., Yoneyama K., et al. Inhibition of shoot branching by new terpenoid plant hormones. Nature 2008, 455:195-200.
25. Vert G., Chory J. Downstream nuclear events in brassinosteroid signalling. Nature 2006, 441:96-100.
26. Wang Z.Y., Nakano T., Gendron J., He J., Chen M., Vafeados D., Yang Y., Fujioka S., Yoshida S., Asami T., Chory J. Nuclear-localized BZR1 mediates brassinosteroid-induced growth and feedback suppression of brassinosteroid biosynthesis. Dev. Cell 2002, 2:505-513.
27. Wang F., Zhu D., Huang X., Li S., Gong Y., Yao Q., Fu X., Fan L.M., Deng X.W. Biochemical insights on degradation of Arabidopsis DELLA proteins gained from a cell-free assay system. Plant Cell 2009, 21:2378-2390.
28. Waters M.T., Nelson D.C., Scaffidi A., Flematti G.R., Sun Y.K., Dixon K.W., Smith S.M. Specialisation within the DWARF14 protein family confers distinct responses to karrikins and strigolactones in Arabidopsis. Development 2012, 139:1285-1295.
29. Yang C.J., Zhang C., Lu Y.N., Jin J.Q., Wang X.L. The mechanisms of brassinosteroids' action: from signal transduction to plant development. Mol. Plant 2011, 4:588-600.
30. Yin Y., Wang Z.Y., Mora-Garcia S., Li J., Yoshida S., Asami T., Chory J. BES1 accumulates in the nucleus in response to brassinosteroids to regulate gene expression and promote stem elongation. Cell 2002, 109:181-191.
31. Yin Y., Vafeados D., Tao Y., Yoshida S., Asami T., Chory J. A new class of transcription factors mediates brassinosteroid-regulated gene expression in Arabidopsis. Cell 2005, 120:249-259.
32. Yu X., Li L., Zola J., Aluru M., Ye H., Foudree A., Guo H., Anderson S., Aluru S., Liu P., et al. A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana. Plant J. 2011, 65:634-646.
33. Zhao L.H., Zhou X.E., Wu Z.S., Yi W., Xu Y., Li S., Xu T.H., Liu Y., Chen R.Z., Kovach A., et al. Crystal structures of two phytohormone signal-transducing α/β hydrolases: karrikin-signaling KAI2 and strigolactone-signaling DWARF14. Cell Res. 2013, 23:436-439.