Divide Et Impera-cellular auxin compartmentalization

Current Opinion in Plant Biology

Volumn 16, Issue 1, 2013, Pages 78-84

  Barbez, Elke ^a,b   Kleine Vehn, Jürgen ^a  

^a UNIVERSITY OF NATURAL RESOURCES AND LIFE SCIENCES   (Austria)

^b GHENT UNIVERSITY   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

INDOLEACETIC ACID DERIVATIVE; PHYTOHORMONE; VEGETABLE PROTEIN;

CELL COMPARTMENTALIZATION; ENDOPLASMIC RETICULUM; HOMEOSTASIS; METABOLISM; PLANT; PLANT DEVELOPMENT; REVIEW; SIGNAL TRANSDUCTION; TRANSPORT AT THE CELLULAR LEVEL;

BIOLOGICAL TRANSPORT; CELL COMPARTMENTATION; ENDOPLASMIC RETICULUM; HOMEOSTASIS; INDOLEACETIC ACIDS; PLANT DEVELOPMENT; PLANT GROWTH REGULATORS; PLANT PROTEINS; PLANTS; SIGNAL TRANSDUCTION;

EID: 84873706405     PISSN: 13695266     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pbi.2012.10.005     Document Type: Review

References (78)

1. von Sachs J. Stoff und Form der Pflanzenorgane I. Arb Bot Inst Wurzburg 1880, 2:452-488.
2. Darwin C., Darwin F. The power of movement in plants. Darwins gesammelte Werke 1881, Bd. 13, Schweizer-bart'sche Verlagsbuchhandlung, Stuttgart, Germany.
3. Went F. On growth-accelerating substances in the coleoptile of Avena sativa. Proc Kon Ned Akad Wet 1926, 30:10-19.
4. Sundberg E., Ostergaard L. Distinct and dynamic auxin activities during reproductive development. Cold Spring Harb Perspect Biol 2009, 1:a001628.
5. Grunewald W., Friml J. The march of the PINs: developmental plasticity by dynamic polar targeting in plant cells. EMBO J 2010, 29:2700-2714.
6. Peris C.I., Rademacher E.H., Weijers D. Green beginnings - pattern formation in the early plant embryo. Curr Top Dev Biol 2010, 91:1-27.
7. Scarpella E., Barkoulas M., Tsiantis M. Control of leaf and vein development by auxin. Cold Spring Harb Perspect Biol 2010, 2:a001511.
8. Zazimalova E., Murphy A.S., Yang H., Hoyerova K., Hosek P. Auxin transporters - why so many?. Cold Spring Harb Perspect Biol 2010, 2:a001552.
9. Woodward A.W., Bartel B. Auxin: regulation, action, and interaction. Ann Bot (Lond) 2005, 95:707-735.
10. Simon S., Petrasek J. Why plants need more than one type of auxin. Plant Sci 2010, 180:454-460.
11. Strader L.C., Bartel B. Transport and metabolism of the endogenous auxin precursor indole-3-butyric acid. Mol Plant 2011, 4:477-486.
12. Dharmasiri N., Dharmasiri S., Estelle M. The F-box protein TIR1 is an auxin receptor. Nature 2005, 435:441-445.
13. Kepinski S., Leyser O. The Arabidopsis F-box protein TIR1 is an auxin receptor. Nature 2005, 435:446-451.
14. Tan X., Calderon-Villalobos L.I., Sharon M., Zheng C., Robinson C.V., Estelle M., Zheng N. Mechanism of auxin perception by the TIR1 ubiquitin ligase. Nature 2007, 446:640-645.
15. Chapman E.J., Estelle M. Mechanism of auxin-regulated gene expression in plants. Annu Rev Genet 2009, 43:265-285.
16. Sauer M., Kleine-Vehn J. AUXIN BINDING PROTEIN1: the outsider. Plant Cell 2011, 23:2033-2043.
17. Braun N., Wyrzykowska J., Muller P., David K., Couch D., Perrot-Rechenmann C., Fleming A.J. Conditional repression of AUXIN BINDING PROTEIN1 reveals that it coordinates cell division and cell expansion during postembryonic shoot development in Arabidopsis and tobacco. Plant Cell 2008, 20:2746-2762.
18. Jurado S., Abraham Z., Manzano C., Lopez-Torrejon G., Pacios L.F., Del Pozo J.C. The Arabidopsis cell cycle F-box protein SKP2A binds to auxin. Plant Cell 2010, 22:3891-3904.
19. Benkova E., Michniewicz M., Sauer M., Teichmann T., Seifertova D., Jurgens G., Friml J. Local, efflux-dependent auxin gradients as a common module for plant organ formation. Cell 2003, 115:591-602.
20. Sorefan K., Girin T., Liljegren S.J., Ljung K., Robles P., Galvan-Ampudia C.S., Offringa R., Friml J., Yanofsky M.F., Ostergaard L. A regulated auxin minimum is required for seed dispersal in Arabidopsis. Nature 2009, 459:583-586.
21. Mravec J., Skupa P., Bailly A., Hoyerova K., Krecek P., Bielach A., Petrasek J., Zhang J., Gaykova V., Stierhof Y.D., et al. Subcellular homeostasis of phytohormone auxin is mediated by the ER-localized PIN5 transporter. Nature 2009, 459:1136-1140.
22. Barbez E., Kubes M., Rolcik J., Beziat C., Pencik A., Wang B., Rosquete M.R., Zhu J., Dobrev P.I., Lee Y., et al. A novel putative auxin carrier family regulates intracellular auxin homeostasis in plants. Nature 2012, 485:119-122.
23. Normanly J. Approaching cellular and molecular resolution of auxin biosynthesis and metabolism. Cold Spring Harb Perspect Biol 2010, 2:a001594.
24. Zhao Y. Auxin biosynthesis and its role in plant development. Annu Rev Plant Biol 2010, 61:49-64.
25. Zhao Y. Auxin biosynthesis: a simple two-step pathway convert tryptophan to indole-3-acetic acid in plants. Mol Plant 2012, 5:334-338.
26. Ruiz Rosquete M., Barbez E., Kleine-Vehn J. Cellular auxin homeostasis: gatekeeping is housekeeping. Mol Plant 2011, 5(4):772-786.
27. Ljung K., Bhalerao R.P., Sandberg G. Sites and homeostatic control of auxin biosynthesis in Arabidopsis during vegetative growth. Plant J 2001, 28:465-474.
28. Ljung K., Hull A.K., Celenza J., Yamada M., Estelle M., Normanly J., Sandberg G. Sites and regulation of auxin biosynthesis in Arabidopsis roots. Plant Cell 2005, 17:1090-1104.
29. Cheng Y., Dai X., Zhao Y. Auxin biosynthesis by the YUCCA flavin monooxygenases controls the formation of floral organs and vascular tissues in Arabidopsis. Genes Dev 2006, 20:1790-1799.
30. Cheng Y., Dai X., Zhao Y. Auxin synthesized by the YUCCA flavin monooxygenases is essential for embryogenesis and leaf formation in Arabidopsis. Plant Cell 2007, 19:2430-2439.
31. Pagnussat G.C., Alandete-Saez M., Bowman J.L., Sundaresan V. Auxin-dependent patterning and gamete specification in the Arabidopsis female gametophyte. Science 2009, 5935:1684-1689.
32. Chandler J.W. Local auxin production: a small contribution to a big field. Bioessays 2009, 31:60-70.
33. Ludwig-Müller J. Auxin conjugates: their role for plant development and in the evolution of land plants. J Exp Bot 2011, 62:1757-1773.
34. Tam Y.Y., Epstein E., Normanly J. Characterization of auxin conjugates in Arabidopsis. Low steady-state levels of indole-3-acetyl-aspartate, indole-3-acetyl-glutamate, and indole-3-acetyl-glucose. Plant Physiol 2000, 123:589-596.
35. Jackson R.G., Lim E.K., Li Y., Kowalczyk M., Sandberg G., Hoggett J., Ashford D.A., Bowles D.J. Identification and biochemical characterization of an Arabidopsis indole-3-acetic acid glucosyltransferase. J Biol Chem 2001, 276:4350-4356.
36. Ludwig-Müller, WAJ., Slovin J.P., Epstein E., Cohen J.D., Dong W., Town C.D. Overexpression of the iaglu gene from maize in Arabidopsis thaliana alters plant growth and sensitivity to IAA but not IBA and 2,4-D. J Plant Growth Regul 2005, 24:127-141.
37. Kowalczyk M., Sandberg G. Quantitative analysis of indole-3-acetic acid metabolites in Arabidopsis. Plant Physiol 2001, 127:1845-1853.
38. Kai K., Horita J., Wakasa K., Miyagawa H. Three oxidative metabolites of indole-3-acetic acid from Arabidopsis thaliana. Phytochemistry 2007, 68:1651-1663.
39. Staswick P.E. The tryptophan conjugates of jasmonic and indole-3-acetic acids are endogenous auxin inhibitors. Plant Physiol 2009, 150:1310-1321.
40. Hagen G., Guilfoyle T.J. Rapid induction of selective transcription by auxins. Mol Cell Biol 1985, 5:1197-1203.
41. Staswick P.E., Serban B., Rowe M., Tiryaki I., Maldonado M.T., Maldonado M.C., Suza W. Characterization of an Arabidopsis enzyme family that conjugates amino acids to indole-3-acetic acid. Plant Cell 2005, 17:616-627.
42. Bartel B., Fink G.R. ILR1, an amidohydrolase that releases active indole-3-acetic acid from conjugates. Science 1995, 268:1745-1748.
43. Davies R.T., Goetz D.H., Lasswell J., Anderson M.N., Bartel B. IAR3 encodes an auxin conjugate hydrolase from Arabidopsis. Plant Cell 1999, 11:365-376.
44. LeClere S., Tellez R., Rampey R.A., Matsuda S.P., Bartel B. Characterization of a family of IAA-amino acid conjugate hydrolases from Arabidopsis. J Biol Chem 2002, 277:20446-20452.
45. Rampey R.A., LeClere S., Kowalczyk M., Ljung K., Sandberg G., Bartel B. A family of auxin-conjugate hydrolases that contributes to free indole-3-acetic acid levels during Arabidopsis germination. Plant Physiol 2004, 135:978-988.
46. Östin A., Kowalyczk M., Bhalerao R.P., Sandberg G. Metabolism of indole-3-acetic acid in Arabidopsis. Plant Physiol 1998, 118:285-296.
47. Ljung K., Ostin A., Lioussanne L., Sandberg G. Developmental regulation of indole-3-acetic acid turnover in Scots pine seedlings. Plant Physiol 2001, 125:464-475.
48. Reinecke D., Bandurski R. Auxin biosynthesis and metabolism. Plant Hormones and Their Role in Plant Growth and Development 1987, Kluwer Academic Publishers, Dordrecht, The Netherlands, 24-42. P.J. Davies (Ed.).
49. Barcelo A., Pedreno M.A., Ferrer M.A., Sabater F., Munoz R. Indole-3-methanol is the main product of the oxidation of indole-3-acetic acid catalyzed by two cytosolic basic isoperoxidases from Lupinus. Planta 1990, 181:448-450.
50. Östin A., Catala C., Chamarro J., Sandberg G. Identification of glucopyranosyl-b-1,4-glucopyranosyl-b-1-N-oxindole-3-acetyl-N-aspartic acid, a new IAA-catabolite with liquid chromatography tandem mass spectrometry. J Mass Spectrom 1995, 30:1007-1017.
51. Riov J., Bangerth F. Metabolism of auxin in tomato fruit tissue: formation of high molecular weight conjugates of oxindole-3-acetic acid via the oxidation of indole-3-acetylaspartic acid. Plant Physiol 1992, 100:1396-1402.
52. Tuominen H., Ostin A., Sandberg G., Sundberg B. A novel metabolic pathway for indole-3-acetic acid in apical shoots of Populus tremula (L.) x Populus tremuloides (Michx.). Plant Physiol 1994, 106:1511-1520.
53. Gonzalez-Lamothe R., El Oirdi M., Brisson N., Bouarab K. The conjugated auxin indole-3-acetic acid-aspartic acid promotes plant disease development. Plant Cell 2012, 24:762-777.
54. Bennett M.J., Marchant A., Green H.G., May S.T., Ward S.P., Millner P.A., Walker A.R., Schulz B., Feldmann K.A. Arabidopsis AUX1 gene: a permease-like regulator of root gravitropism. Science 1996, 273:948-950.
55. Gälweiler L., Guan C., Müller A., Wisman E., Mendgen K., Yephremov A., Palme K. Regulation of polar auxin transport by AtPIN1 in Arabidopsis vascular tissue. Science 1998, 282:2226-2230.
56. Luschnig C., Gaxiola R.A., Grisafi P., Fink G.R. EIR1, a root-specific protein involved in auxin transport, is required for gravitropism in Arabidopsis thaliana. Genes Dev 1998, 12:2175-2187.
57. Friml J., Benkova E., Blilou I., Wisniewska J., Hamann T., Ljung K., Woody S., Sandberg G., Scheres B., Jurgens G., et al. AtPIN4 mediates sink-driven auxin gradients and root patterning in Arabidopsis. Cell 2002, 108:661-673.
58. Friml J., Wisniewska J., Benkova E., Mendgen K., Palme K. Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis. Nature 2002, 415:806-809.
59. Murphy A.S., Hoogner K.R., Peer W.A., Taiz L. Identification, purification, and molecular cloning of N-1-naphthylphthalmic acid-binding plasma membrane-associated aminopeptidases from Arabidopsis. Plant Physiol 2002, 238:935-950.
60. Friml J., Palme K. Polar auxin transport - old questions and new concepts?. Plant Mol Biol 2002, 49:273-284.
61. Geisler M., Blakeslee J.J., Bouchard R., Lee O.R., Vincenzetti V., Bandyopadhyay A., Titapiwatanakun B., Peer W.A., Bailly A., Richards E.L., et al. Cellular efflux of auxin catalyzed by the Arabidopsis MDR/PGP transporter AtPGP1. Plant J 2005, 44:179-194.
62. Friml et al. 2013, this issue.
63. Peer W.A., Blakeslee J.J., Yang H., Murphy A.S. Seven things we think we know about auxin transport. Mol Plant 2011, 4:487-504.
64. Kramer E.M., Bennett M.J. Auxin transport: a field in flux. Trends Plant Sci 2006, 11:386-396.
65. Bosco C.D., Dovzhenko A., Liu X., Woerner N., Rensch T., Eismann M., Eimer S., Hegermann J., Paponov I.A., Ruperti B., et al. The endoplasmic reticulum localized PIN8 is a pollen-specific auxin carrier involved in intracellular auxin homeostasis. Plant J 2012, 71:860-870.
66. Ding Z., Wang B., Moreno I., Duplakova N., Simon S., Carraro N., Reemmer J., Pencik A., Chen X., Tejos R., et al. ER-localized auxin transporter PIN8 regulates auxin homeostasis and male gametophyte development in Arabidopsis. Nat Commun 2012, 3:941.
67. Yang H., Murphy A.S. Functional expression and characterization of Arabidopsis ABCB, AUX 1 and PIN auxin transporters in Schizosaccharomyces pombe. Plant J 2009, 59(1):179-191.
68. Feraru E., Vosolsobe S., Feraru M.I., Petrášek J., Kleine-Vehn J. Evolution and structural diversification of PILS putative auxin carriers in plants. Front Plant Sci 2012, 3:227.
69. Viaene T., Delwiche C.F., Rensing S.A., Friml J. Origin and evolution of PIN auxin transporters in the green lineage. Trends Plant Sci 2012, 10.1016/j.tplants.2012.08.009.
70. Ludwig-Muller J., Decker E.L., Reski R. Dead end for auxin conjugates in Physcomitrella?. Plant Signal Behav 2009, 4:116-118.
71. Ludwig-Muller J., Julke S., Bierfreund N.M., Decker E.L., Reski R. Moss (Physcomitrella patens) GH3 proteins act in auxin homeostasis. New Phytol 2009, 181:323-338.
72. Campanella J.J., Larko D., Smalley J. A molecular phylogenomic analysis of the ILR1-like family of IAA amidohydrolase genes. Comp Funct Genomics 2003, 4:584-600.
73. Bitto E., Bingman C.A., Bittova L., Houston N.L., Boston R.S., Fox B.G., Phillips G.N. X-ray structure of ILL2, an auxin-conjugate amidohydrolase from Arabidopsis thaliana. Proteins 2009, 74:61-71.
74. Kriechbaumer V., Wang P., Hawes C., Abell B.M. Alternative splicing of the auxin biosynthesis gene YUCCA4 determines its subcellular compartmentation. Plant J 2012, 70:292-302.
75. Jones A.M., Herman E.M. KDEL-containing auxin-binding protein is secreted to the plasma membrane and cell wall. Plant Physiol 1993, 101:595-606.
76. Henderson J., Bauly J.M., Ashford D.A., Oliver S.C., Hawes C.R., Lazarus C.M., Venis M.A., Napier R.M. Retention of maize auxin-binding protein in the endoplasmic reticulum: quantifying escape and the role of auxin. Planta 1997, 202:3-323.
77. Tian H., Klambt D., Jones A.M. Auxin-binding protein 1 does not bind auxin within the endoplasmic reticulum despite this being the predominant subcellular location for this hormone receptor. J Biol Chem 1995, 270:26962-26969.
78. Wabnik K., Kleine-Vehn J., Govaerts W., Friml J. Prototype cell-to-cell auxin transport mechanism by intracellular auxin compartmentalization. Trends Plant Sci 2011, 16:468-475.