1 |
Guzman, P., and Ecker, J.R. (1990). Exploiting the triple response of Arabidopsis to identify ethylene-related mutants. Plant Cell 2, 513-523.
DOI
ScienceOn
|
2 |
Hansen, M., Chae, H.S., and Kieber, J.J. (2009). Regulation of ACS protein stability by cytokinin and brassinosteroid. Plant J. 57, 606-614.
DOI
ScienceOn
|
3 |
Harpaz-Saad, S., Yoon, G.M., Matto, A.K., and Kieber, J.J. (2012). The formation of ACC and competition between polyamines and ethylene for SAM. Annu. Plant Rev. 44, 53-81.
|
4 |
Hernandez Sebastia, C., Hardin, S.C., Clouse, S.D., Kieber, J.J., and Huber, S.C. (2004). Identification of a new motif for CDPK phosphorylation in vitro that suggests ACC synthase may be a CDPK substrate. Arch. Biochem. Biophys. 428, 81-91.
DOI
ScienceOn
|
5 |
Ho, M.S., Ou, C., Chan, Y.R., Chien, C.T., and Pi, H. (2008). The utility F-box for protein destruction. Cell. Mol. Life Sci. 65, 1977-2000.
DOI
|
6 |
Holt, L.J., Tuch, B.B., Villen, J., Johnson, A.D., Gygi, S.P., and Morgan, D.O. (2009). Global analysis of Cdk1 substrate phosphorylation sites provides insights into evolution. Science 325, 1682-1686.
DOI
ScienceOn
|
7 |
Joo, S., Liu, Y., Lueth, A., and Zhang, S. (2008). MAPK phosphorylation-induced stabilization of ACS6 protein is mediated by the non-catalytic C-terminal domain, which also contains the cis-determinant for rapid degradation by the 26S proteasome pathway. Plant J. 54, 129-140.
DOI
ScienceOn
|
8 |
Kamiyoshihara, Y., Iwata, M., Fukaya, T., Tatsuki, M., and Mori, H. (2010). Turnover of LeACS2, a wound-inducible 1-aminocyclopropane-1-carboxylic acid synthase in tomato, is regulated by phosphorylation/dephosphorylation. Plant J. 64, 140-150.
|
9 |
Kende, H. (1993). Ethylene biosynthesis. Annu. Rev. Plant Physiol. Plant Mol. Biol. 44, 283-307.
DOI
|
10 |
Kim, C.Y., Liu, Y., Thorne, E.T., Yang, H., Fukushige, H., Gassmann, W., Hildebrand, D., Sharp, R.E., and Zhang, S. (2003). Activation of a stress-responsive mitogen-activated protein kinase cascade induces the biosynthesis of ethylene in plants. Plant Cell 15, 2707-2718.
DOI
ScienceOn
|
11 |
Knight, L.I., Rose, R.C., and Crocker, W. (1910). Effects of various gases and vapors upon etiolated seedlings of the sweet pea. Science 31, 635-636.
|
12 |
Lara, I., and Vendrell, M. (2000). Development of ethylenesynthesizing capacity in preclimacteric apples: interaction between abscisic acid and ethylene. J. Am. Soc. Hortic. Sci. 125, 505-512.
|
13 |
Larsen, P.B., and Cancel, J.D. (2004). A recessive mutation in the RUB1-conjugating enzyme, RCE1, reveals a requirement for RUB modification for control of ethylene biosynthesis and proper induction of basic chitinase and PDF1.2 in Arabidopsis. Plant J. 38, 626-638.
DOI
ScienceOn
|
14 |
Li, C.H., Wang, G., Zhao, J.L., Zhang, L.Q., Ai, L.F., Han, Y.F., Sun, D.Y., Zhang, S.W., and Sun, Y. (2014). The Receptor-Like Kinase SIT1 Mediates Salt Sensitivity by Activating MAPK3/6 and regulating ethylene homeostasis in rice. Plant Cell 26, 2538-2553.
DOI
ScienceOn
|
15 |
Lieberman, M., and Mapson, L.W. (1964). Genesis and biogenesis of ethylene. Nature 204, 343-345.
DOI
|
16 |
Liu, Y., and Zhang, S. (2004). Phosphorylation of 1-aminocyclopropane-1-carboxylic acid synthase by MPK6, a stressresponsive mitogen-activated protein kinase, induces ethylene biosynthesis in Arabidopsis. Plant Cell 16, 3386-3399.
DOI
ScienceOn
|
17 |
Liu, W., Xu, Z.H., Luo, D., and Xue, H.W. (2003). Roles of OsCKI1, a rice casein kinase I, in root development and plant hormone sensitivity. Plant J. 36, 189-202.
DOI
ScienceOn
|
18 |
Mayfield, J.D., Folta, K.M., Paul, A.L., and Ferl, R.J. (2007). The 14-3-3 Proteins mu and upsilon influence transition to flowering and early phytochrome response. Plant Physiol. 145, 1692-1702.
DOI
ScienceOn
|
19 |
Lyzenga, W.J., Booth, J.K., and Stone, S.L. (2012). The Arabidopsis RING-type E3 ligase XBAT32 mediates the proteasomal degradation of the ethylene biosynthetic enzyme, 1-aminocyclopropane-1-carboxylate synthase 7. Plant J. 71, 23-34.
DOI
ScienceOn
|
20 |
Mattoo, A.K., and Suttle, J.C. (1991). The Plant Hormone Ethylene. (Boca Raton: CRC Press).
|
21 |
McClellan, C.A., and Chang, C.L. (2008). The role of protein turnover in ethylene biosynthesis and response. Plant Sci. 175, 24-31.
DOI
ScienceOn
|
22 |
Murr, D.P., and Yang, S.F. (1975). Conversion of 5-methylthioadenosine to methionine by apple tissue. Phytochemistry 14, 1291-1292.
DOI
ScienceOn
|
23 |
Neljubov, D. (1901). Uber die horizontale Nutation der Stengel von Pisum sativum und einiger Anderer. Pflanzen Beih. Bot. Zentralb 10, 128-139.
|
24 |
Nodzon, L.A., Xu, W.H., Wang, Y., Pi, L.Y., Chakrabarty, P.K., and Song, W.Y. (2004). The ubiquitin ligase XBAT32 regulates lateral root development in Arabidopsis. Plant J. 40, 996-1006.
DOI
ScienceOn
|
25 |
Paul, A.L., Folta, K.M., and Ferl, R.J. (2008). 14-3-3 proteins, red light and photoperiodic flowering: a point of connection? Plant Signal. Behav. 3, 511-515.
DOI
|
26 |
Paul, A.L., Denison, F.C., Schultz, E.R., Zupanska, A.K., and Ferl, R.J. (2012). 14-3-3 phosphoprotein interaction networks-does isoform diversity present functional interaction specification? Front. Plant Sci. 3, 190.
|
27 |
Sauter, M., Moffatt, B., Saechao, M.C., Hell, R., and Wirtz, M. (2013). Methionine salvage and Sadenosylmethionine: essential links between sulfur, ethylene and polyamine biosynthesis. Biochem. J. 451, 145-154.
DOI
|
28 |
Pintard, L., Willems, A., and Peter, M. (2004). Cullin-based ubiquitin ligases: Cul3-BTB complexes join the family. EMBO J. 23, 1681-1687.
DOI
ScienceOn
|
29 |
Prasad, M.E., Schofield, A., Lyzenga, W., Liu, H., and Stone, S.L. (2010). Arabidopsis RING E3 ligase XBAT32 regulates lateral root production through its role in ethylene biosynthesis. Plant Physiol. 153, 1587-1596.
DOI
ScienceOn
|
30 |
Purwestri, Y.A., Ogaki, Y., Tamaki, S., Tsuji, H., and Shimamoto, K. (2009). The 14-3-3 protein GF14c acts as a negative regulator of flowering in rice by interacting with the florigen Hd3a. Plant Cell Physiol. 50, 429-438.
DOI
ScienceOn
|
31 |
Skottke, K.R., Yoon, G.M., Kieber, J.J., and DeLong, A. (2011). Protein phosphatase 2A controls ethylene biosynthesis by differentially regulating the turnover of ACC synthase isoforms. PLoS Genet. 7, e1001370.
DOI
ScienceOn
|
32 |
Su, C.H., Zhao, R., Zhang, F., Qu, C., Chen, B., Feng, Y.H., Phan, L., Chen, J., Wang, H., Wang, H., et al. (2011). 14-3-3sigma exerts tumor-suppressor activity mediated by regulation of COP1 stability. Cancer Res. 71, 884-894.
DOI
|
33 |
Tan, S.T., and Xue, H.W. (2014). Casein kinase 1 regulates ethylene synthesis by phosphorylating and promoting the turnover of ACS5. Cell Rep. 9, 1692-1702.
DOI
ScienceOn
|
34 |
Tan, S.T., Dai, C., Liu, H.T., and Xue, H.W. (2013). Arabidopsis casein kinase1 proteins CK1.3 and CK1.4 phosphorylate cryptochrome2 to regulate blue light signaling. Plant Cell 25, 2618-2632.
DOI
ScienceOn
|
35 |
Van de Poel, B., and Van Der Straeten, D. (2014). 1-aminocyclopropane-1-carboxylic acid (ACC) in plants: more than just the precursor of ethylene! Front. Plant Sci. 5, 640.
|
36 |
Tari, I., and Nagy, M. (1996). Abscisic acid and ethrel abolish the inhibition of adventitious root formation of pacrobutrazol-treated bean primary leaf cuttings. Biol. Plant. 38, 369-375.
DOI
|
37 |
Tseng, T.S., Whippo, C., Hangarter, R.P., and Briggs, W.R. (2012). The role of a 14-3-3 protein in stomatal opening mediated by PHOT2 in Arabidopsis. Plant Cell 24, 1114-1126.
DOI
ScienceOn
|
38 |
Tsuchisaka, A., and Theologis, A. (2004). Unique and overlapping expression patterns among the Arabidopsis 1-aminocyclopropane-1-carboxylate synthase gene family members. Plant Physiol. 136, 2982-3000.
DOI
ScienceOn
|
39 |
Vogel, J.P., Woeste, K.E., Theologis, A., and Kieber, J.J. (1998). Recessive and dominant mutations in the ethylene biosynthetic gene ACS5 of Arabidopsis confer cytokinin insensitivity and ethylene overproduction, respectively. Proc. Natl. Acad. Sci. USA 95, 4766-4771.
DOI
|
40 |
Vriezen, W.H., Hulzink, R., Mariani, C., and Voesenek, L.A. (1999). 1-aminocyclopropane-1-carboxylate oxidase activity limits ethylene biosynthesis in Rumex palustris during submergence. Plant Physiol. 121, 189-196.
DOI
|
41 |
Wang, K.L., Yoshida, H., Lurin, C., and Ecker, J.R. (2004). Regulation of ethylene gas biosynthesis by the Arabidopsis ETO1 protein. Nature 428, 945-950.
DOI
ScienceOn
|
42 |
Wee, S., Geyer, R.K., Toda, T., and Wolf, D.A. (2005). CSN facilitates Cullin-RING ubiquitin ligase function by counteracting autocatalytic adapter instability. Nat. Cell Biol. 7, 387-391.
DOI
ScienceOn
|
43 |
Yang, S.F., and Hoffman, N.E. (1984). Ethylene biosynthesis and its regulation in higher plants.. Ann. Rev. Plant Physiol. 34, 34.
|
44 |
Woeste, K.E., Vogel, J.P., and Kieber, J.J. (1999a). Factors regulating ethylene biosynthesis in etiolated Arabidopsis thaliana seedlings. Physiol. Plant. 105, 478-484.
DOI
ScienceOn
|
45 |
Woeste, K.E., Ye, C., and Kieber, J.J. (1999b). Two Arabidopsis mutants that overproduce ethylene are affected in the posttranscriptional regulation of 1-aminocyclopropane-1-carboxylic acid synthase. Plant Physiol. 119, 521-530.
DOI
|
46 |
Xiong, L., Xiao, D., Xu, X., Guo, Z., and Wang, N.N. (2014). The non-catalytic N-terminal domain of ACS7 is involved in the posttranslational regulation of this gene in Arabidopsis. J. Exp. Bot. 65, 4397-4408.
DOI
ScienceOn
|
47 |
Yang, H.Y., Wen, Y.Y., Lin, Y.I., Pham, L., Su, C.H., Yang, H., Chen, J., and Lee, M.H. (2007). Roles for negative cell regulator 14-3-3sigma in control of MDM2 activities. Oncogene 26, 7355-7362.
DOI
ScienceOn
|
48 |
Yi, H.C., Joo, S., Nam, K.H., Lee, J.S., Kang, B.G., and Kim, W.T. (1999). Auxin and brassinosteroid differentially regulate the expression of three members of the 1-aminocyclopropane-1-carboxylate synthase gene family in mung bean (Vigna radiata L.). Plant Mol. Biol. 41, 443-454.
DOI
ScienceOn
|
49 |
Yoon, G.M., and Kieber, J.J. (2013a). 14-3-3 regulates 1-aminocyclopropane-1-carboxylate synthase protein turnover in Arabidopsis. Plant Cell 25, 1016-1028.
DOI
ScienceOn
|
50 |
Yoon, G.M., and Kieber, J.J. (2013b). ACC synthase and its cognate E3 ligase are inversely regulated by light. Plant Signal. Behav. 8, e26478.
DOI
|
51 |
Zhang, M., Yuan, B., and Leng, P. (2009). The role of ABA in triggering ethylene biosynthesis and ripening of tomato fruit. J. Exp. Bot. 60, 1579-1588.
DOI
ScienceOn
|
52 |
Yoshida, H., Nagata, M., Saito, K., Wang, K.L., and Ecker, J.R. (2005). Arabidopsis ETO1 specifically interacts with and negatively regulates type 2 1-aminocyclopropane-1-carboxylate synthases. BMC Plant Biol. 5, 14.
DOI
ScienceOn
|
53 |
Yoshida, H., Wang, K.L., Chang, C.M., Mori, K., Uchida, E., and Ecker, J.R. (2006). The ACC synthase TOE sequence is required for interaction with ETO1 family proteins and destabilization of target proteins. C 62, 427-437.
DOI
|
54 |
Zarembinski, T.I., and Theologis, A. (1994). Ethylene biosynthesis and action: a case of conservation. The 26, 1579-1597.
DOI
|
55 |
Arteca, R.N., and Arteca, J.M. (2008). Effects of brassinosteroid, auxin, and cytokinin on ethylene production in Arabidopsis thaliana plants. J. Exp. Bot. 59, 3019-3026.
DOI
ScienceOn
|
56 |
Abeles, F.B., Morgan, P.W., and Saltveit, M.E.J. (1992). Ethylene in plant biology. (San Diego, CA: Academic Press)
|
57 |
Adams, D.O., and Yang, S.F. (1977). Methionine metabolism in apple tissue-implication of S-adenosylmethionine as an intermediate in conversion of methionine to ethylene. Plant Physiol. 60, 892-896.
DOI
ScienceOn
|
58 |
Aitken, A., Collinge, D.B., van Heusden, B.P., Isobe, T., Roseboom, P.H., Rosenfeld, G., and Soll, J. (1992). 14-3-3 proteins: a highly conserved, widespread family of eukaryotic proteins. Trends Biochem Sci. 17, 498-501.
DOI
ScienceOn
|
59 |
Albagli, O., Dhordain, P., Deweindt, C., Lecocq, G., and Leprince, D. (1995). The BTB/POZ domain: a new protein-protein interaction motif common to DNA-and actin-binding proteins. Cell Growth Differ. 6, 1193-1198.
|
60 |
Argueso, C.T., Hansen, M., and Kieber, J.J. (2007). Regulation of ethylene biosynthesis.. J. Plant Growth Regul. 26, 13.
|
61 |
Ben-Nissan, G., Cui, W., Kim, D.J., Yang, Y., Yoo, B.C., and Lee, J.Y. (2008). Arabidopsis casein kinase 1-like 6 contains a microtubule-binding domain and affects the organization of cortical microtubules. Plant Physiol. 148, 1897-1907.
DOI
ScienceOn
|
62 |
Blatch, G.L., and Lassle, M. (1999). The tetratricopeptide repeat: a structural motif mediating protein-protein interactions. BioEssays 21, 932-939.
DOI
|
63 |
Boller, T., Herner, R.C., and Kende, H. (1979). Assay for and enzymatic formation of an ethylene precursor, 1-aminocyclopropane-1-carboxylic acid. Planta 145, 293-303.
DOI
ScienceOn
|
64 |
Bornke, F. (2005). The variable C-terminus of 14-3-3 proteins mediates isoform-specific interaction with sucrose-phosphate synthase in the yeast two-hybrid system. J. Plant Physiol. 162, 161-168.
DOI
ScienceOn
|
65 |
Bostick, M., Lochhead, S.R., Honda, A., Palmer, S., and Callis, J. (2004). Related to ubiquitin 1 and 2 are redundant and essential and regulate vegetative growth, auxin signaling, and ethylene production in Arabidopsis. Plant Cell 16, 2418-2432.
DOI
ScienceOn
|
66 |
Christians, M.J., Gingerich, D.J., Hansen, M., Binder, B.M., Kieber, J.J., and Vierstra, R.D. (2009). The BTB ubiquitin ligases ETO1, EOL1 and EOL2 act collectively to regulate ethylene biosynthesis in Arabidopsis by controlling type-2 ACC synthase levels. Plant J. 57, 332-345.
DOI
ScienceOn
|
67 |
Catala, R., Lopez-Cobollo, R., Mar Castellano, M., Angosto, T., Alonso, J.M., Ecker, J.R., and Salinas, J. (2014). The Arabidopsis 14-3-3 protein RARE COLD INDUCIBLE 1A links lowtemperature response and ethylene biosynthesis to regulate freezing tolerance and cold acclimation. Plant Cell 26, 3326-3342.
DOI
ScienceOn
|
68 |
Chae, H.S., and Kieber, J.J. (2005). Eto Brute? Role of ACS turnover in regulating ethylene biosynthesis. Trends Plant Sci. 10, 291-296.
DOI
ScienceOn
|
69 |
Chae, H.S., Faure, F., and Kieber, J.J. (2003). The eto1, eto2, and eto3 mutations and cytokinin treatment increase ethylene biosynthesis in Arabidopsis by increasing the stability of ACS protein. Plant Cell 15, 545-559.
DOI
|
70 |
Crocker, W., and Knight, L.I. (1908). Effect of illuminating gas and ethylene upon flowering carnation. Bot. Gaz 46, 259-276.
DOI
ScienceOn
|
71 |
Dai, C., and Xue, H.W. (2010). Rice early flowering1, a CKI, phosphorylates DELLA protein SLR1 to negatively regulate gibberellin signalling. EMBO J. 29, 1916-1927.
DOI
ScienceOn
|
72 |
Darling, D.L., Yingling, J., and Wynshaw-Boris, A. (2005). Role of 14-3-3 proteins in eukaryotic signaling and development. Curr. Top. Dev. Biol. 68, 281-315.
DOI
ScienceOn
|
73 |
De Boer, A.H., van Kleeff, P.J., and Gao, J. (2013). Plant 14-3-3 proteins as spiders in a web of phosphorylation. Protoplasma 250, 425-440.
DOI
ScienceOn
|
74 |
Dong, J.G., Fernandez-Maculet, J.C., and Yang, S.F. (1992). Purification and characterization of 1-aminocyclopropane-1-carboxylate oxidase from apple fruit. Proc. Natl. Acad. Sci. USA 89, 9789-9793.
DOI
ScienceOn
|
75 |
De Grauwe, L., Chaerle, L., Dugardeyn, J., Decat, J., Rieu, I., Vriezen, W.H., Baghour, M., Moritz, T., Beemster, G.T., Phillips, A.L., et al. (2008a). Reduced gibberellin response affects ethylene biosynthesis and responsiveness in the Arabidopsis gai eto2-1 double mutant. New Phytol. 177, 128-141.
|
76 |
De Grauwe, L., Dugardeyn, J., and Van Der Straeten, D. (2008b). Novel mechanisms of ethylene-gibberellin crosstalk revealed by the gai eto2-1 double mutant. Plant Signal. Behav. 3, 1113-1115.
DOI
|
77 |
Denison, F.C., Paul, A.L., Zupanska, A.K., and Ferl, R.J. (2011). 14-3-3 proteins in plant physiology. Semin. Cell Dev. Biol. 22, 720-727.
DOI
ScienceOn
|
78 |
Dougherty, M.K., and Morrison, D.K. (2004). Unlocking the code of 14-3-3. J. Cell Sci. 117, 1875-1884.
DOI
ScienceOn
|
79 |
Freeman, A.K., and Morrison, D.K. (2011). 14-3-3 Proteins: diverse functions in cell proliferation and cancer progression. Semin. Cell Dev. Biol. 22, 681-687.
DOI
ScienceOn
|
80 |
Fu, H., Subramanian, R.R., and Masters, S.C. (2000). 14-3-3 proteins: structure, function, and regulation. Annu. Rev. Pharmacol. Toxicol. 40, 617-647.
DOI
ScienceOn
|
81 |
Gane, R. (1934). Production of ethylene by some ripening fruits. Nature 134, 1008-1008
|
82 |
Ganguly, S., Weller, J.L., Ho, A., Chemineau, P., Malpaux, B., and Klein, D.C. (2005). Melatonin synthesis: 14-3-3-dependent activation and inhibition of arylalkylamine N-acetyltransferase mediated by phosphoserine-205. Proc. Natl. Acad. Sci. USA 102, 1222-1227.
DOI
ScienceOn
|