Ethylene and Auxin Control the Arabidopsis Response to Decreased Light Intensity
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Abel S, Nguyen MD, Chow W, Theologis A (1995) ACS4, a primary indole acetic acid-responsive gene encoding 1-aminocyclopropane-1-carboxylate synthase in Arabidopsis thaliana. J Biol Chem 270 : 26020–26020
Ainley WM, Walker JC, Nagao RT, Key JL (1988) Sequence and characterization of 2 auxin-regulated genes from soybean. J Biol Chem 63 : 10658–10666
Al Shehbaz IA, O'Kane SL (2002) Taxonomy and phylogeny of Arabidopsis (Brassicaceae). In CR Somerville, EM Meyerowitz, eds, The Arabidopsis Book. American Society of Plant Biologists, Rockville, MD, doi/10.1199/tab.0001, http://www.aspb.org/publications/arabidopsis
Bassi PK, Spencer MS (1983) Does light inhibit ethylene production in leaves? Plant Physiol 73 : 758–760
Bijnen FGC, Reuss J, Harren FJM (1996) Geometrical optimization of a longitudinal resonant photoacoustic cell for sensitive and fast trace gas detection. Rev Sci Instrum 67 : 2914–2923
Blackman GE, Wilson GL (1951) Physiological and ecological studies in the analysis of plant environment: VII. An analysis of the differential effects of light intensity on the net assimilation rate, leaf-area ratio, and relative growth rate of different species. Ann Bot 15 : 373–408
Breyne P, Dreesen R, Vandepoele K, De Veylder L, Van Breusegem F, Callewaert L, Rombauts S, Raes J, Cannoot B, Engler G et al. (2002) Transcriptome analysis during cell division in plants. Proc Natl Acad Sci USA 99 : 14825–14830
Brock TG, Ghosheh NS, Kaufman PB (1994) Differential sensitivity to indole-3-acetic acid and gibberellic acid following gravistimulation of the leaf sheath pulvini of oat and barley. Plant Physiol Biochem 32 : 487–491
Chae HS, Faure F, Kieber JJ (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
Chang C, Kwok SF, Bleecker AB, Meyerowitz EM (1993) Arabidopsis ethylene response gene ETR1: Similarity of product to two-component regulators. Science 262 : 539–544
Chapin FS, Walker LR, Fastie CL, Sharman LC (1994) Mechanisms of primary succession following deglaciation at Glacier Bay, Alaska. Ecol Monogr 64 : 149–175
Chatfield SP, Stirnberg P, Forde BG, Leyser O (2000) The hormonal regulation of axillary bud growth in Arabidopsis. Plant J 24 : 159–169
Clack T, Mathews S, Sharrock RA (1994) The phytochrome apoprotein family in Arabidopsis is encoded by 5 genes: the sequences and expression of PHYD and PHYE. Plant Mol Biol 25 : 413–427
Clua A, Bottini R, Brocchi GN, Bogino J, Luna V, Montaldi ER (1996) Growth habit of Lotus tenuis shoots and the influence of photosynthetic photon flux density, sucrose and endogenous levels of gibberellins A-1 and A-3. Physiol Plant 98 : 381–388
Colon-Carmona A, Chen DL, Yeh KC, Abel S (2000) AUX/IAA proteins are phosphorylated by phytochrome in vitro. Plant Physiol 124 : 1728–1738
Corbineau F, Rudnicki RM, Goszczynska DM, Come D (1995) The effect of light quality on ethylene production in leaves of oat seedlings (Avena sativa L.). Environ Exp Bot 35: 227–233
Cox MCH, Millenaar FF, de Jong van Berkel YEM, Peeters AJM, Voesenek LACJ (2003) Plant movement: submergence-induced petiole elongation in Rumex palustris depends on hyponastic growth. Plant Physiol 132 : 282–291
Dedonder A, Rethy R, Fredericq H, Van Montagu M, Krebbers E (1993) Arabidopsis RBCS genes are differentially regulated by light. Plant Physiol 101 : 801–808
De Laat AMM, Brandenburg DCC, van Loon LC (1981) The modulation of the conversion of 1-aminocyclopropane-1-carboxylic acid to ethylene by light. Planta 153 : 193–200
Devlin PF, Halliday KJ, Harberd NP, Whitelam GC (1996) The rosette habit of Arabidopsis thaliana is dependent upon phytochrome action: novel phytochromes control internode elongation and flowering time. Plant J 10 : 1127–1134
Finlayson SA, Lee IJ, Morgan PW (1998) Phytochrome B and the regulation of circadian ethylene production in sorghum. Plant Physiol 116 : 17–25
Finlayson SA, Lee IJ, Mullet JE, Morgan PW (1999) The mechanism of rhythmic ethylene production in sorghum: the role of phytochrome B and simulated shading. Plant Physiol 119 : 1083–1089
Friml J, Wisniewska J, Benkova E, Mendgen K, Palme K (2002) Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis. Nature 415 : 806–809
Guzmán P, Ecker JR (1990) Exploiting the triple response of Arabidopsis to identify ethylene-related mutants. Plant Cell 2 : 513–523
Hansen H, Grossmann K (2000) Auxin-induced ethylene triggers abscisic acid biosynthesis and growth inhibition. Plant Physiol 124 : 1437–1448
Harper RM, Stowe-Evans EL, Luesse DR, Muto H, Tatematsu K, Watahiki MK, Yamamoto K, Liscum E (2000) The NPH4 locus encodes the auxin response factor ARF7, a conditional regulator of differential growth in aerial Arabidopsis tissue. Plant Cell 12 : 757–770
Herbert TJ (1983) The influence of axial rotation upon interception of direct solar radiation by plant leaves. J Theor Biol 105 : 603–618
Hirayama T, Kieber JJ, Hirayama N, Kogan M, Guzman P, Nourizadeh S, Alonso JM, Dailey WP, Dancis A, Ecker JR (1999) Responsive-to-antagonist1, a Menkes/Wilson disease-related copper transporter, is required for ethylene signaling in Arabidopsis. Cell 97 : 383–393
Holmes MG (1983) Perception of shade. Philos Trans R Soc Lond B 303 : 503–521
Kao CH, Yang SF (1982) Light inhibition of the conversion of 1-aminocyclopropane carboxylic acid to ethylene in leaves is mediated through carbon dioxide. Planta 155 : 261–266
Kieber JJ, Rothenberg M, Roman G, Feldmann KA, Ecker JR (1993) CTR1, a negative regulator of the ethylene response pathway in Arabidopsis, encodes a member of the Raf family of protein kinases. Cell 72 : 427–441
Kim BC, Soh MS, Kang BJ, Furuya M, Nam HG (1996) Two dominant photomorphogenic mutations of Arabidopsis thaliana identified as suppressor mutations of hy2. Plant J 9 : 441–456
Lehman A, Black R, Ecker JR (1996) HOOKLESS1, an ethylene response gene, is required for differential cell elongation in the Arabidopsis hypocotyl. Cell 85 : 183–194
Lippincott BB, Lippincott JA (1971) Auxin-induced hyponasty of the leaf blade of Phaseolus vulgaris. Am J Bot 58 : 817–826
Luschnig C, Gaxiola RA, Grisafi P, Fink GR (1998) EIR1, a root-specific protein involved in auxin transport, is required for gravitropism in Arabidopsis thaliana. Genes Dev 12 : 2175–2187
Koornneef M, Rolff E, Spruit CJP (1980) Genetic-control of light-inhibited hypocotyl elongation in Arabidopsis thaliana (L) Heynh. Z Pflanzenphysiol 100 : 147–160
Madlung A, Behringer FJ, Lomax TL (1999) Ethylene plays multiple non-primary roles in modulating the gravitropic response in tomato. Plant Physiol 120 : 897–906
Maliakal SK, McDonnell K, Dudley SA, Schmitt J (1999) Effects of red to far-red ratio and plant density on biomass allocation and gas exchange in Impatiens capensis. Int J Plant Sci 160 : 723–733
McConnaughay KDM, Coleman JS (1999) Biomass allocation in plants: ontogeny or optimality? A test along three resource gradients. Ecology 80 : 2581–2593
Müller A, Guan C, Galweiler L, Tanzler P, Huijser P, Marchant A, Darry G, Bennett M, Wisman E, Palme K (1998) AtPIN2 defines a locus of Arabidopsis for root gravitropism control. EMBO J 17 : 6903–6911
Pigliucci M, Schmitt J (1999) Genes affecting phenotypic plasticity in Arabidopsis: pleiotropic effects and reproductive fitness of photomorphogenic mutants. Evol Biol 12 : 551–562
Reed JW, Nagpal P, Poole DS, Furuya M, Chory J (1993) Mutations in the gene for the red/far-red light receptor phytochrome B alter cell elongation and physiological responses throughout Arabidopsis development. Plant Cell 5 : 147–157
Robson PRH, Whitelam GC, Smith H (1993) Selected Components of the shade-avoidance syndrome are displayed in a normal manner in mutants of Arabidopsis thaliana and Brassica rapa deficient in phytochrome. Plant Physiol 102 : 1179–1184
Rodrigues-Pousada RA, De Rycke R, Dedonder A, Van Caeneghem W, Engler G, Van Montagu M, Van Der Straeten D (1993) The Arabidopsis 1-aminocyclopropane-1-carboxylate synthase gene 1 is expressed during early development. Plant Cell 5 : 897–911
Rudnicki RM, Fjeld T, Moe R (1993) Effect of light quality on ethylene formation in leaf and petal disks of Begonia × hiemalis-Fotsch cv Schwabenland red. Plant Growth Regul 13 : 281–286
Sawa S, Ohgishi M, Goda H, Higuchi K, Shimada Y, Yoshida S, Koshiba T (2002) The HAT2 gene, a member of the HD-Zip gene family, isolated as an auxin inducible gene by DNA microarray screening, affects auxin response in Arabidopsis. Plant J 32 : 1011–1022
Smalle J, Haegman M, Kurepa J, Van Montagu M, Van Der Straeten D (1997) Ethylene can stimulate Arabidopsis hypocotyl elongation in the light. Proc Natl Acad Sci USA 94 : 2756–2761
Smith H (1992) The ecological functions of the phytochrome family: clues to a transgenic programme of crop improvement. Photochem Photobiol 56 : 815–822
Smith H, Whitelam GC (1997) The shade avoidance syndrome: multiple responses mediated by multiple phytochromes. Plant Cell Environ 20 : 840–844
Somers DE, Sharrock RA, Tepperman JM, Quail PH (1991) The Hy3 long hypocotyl mutant of Arabidopsis is deficient in phytochrome-B. Plant Cell 3 : 1263–1274
Steindler C, Matteucci A, Sessa G, Weimar T, Ohgishi M, Aoyama T, Morelli G, Ruberti I (1999) Shade avoidance responses are mediated by the ATHB-2 HD-Zip protein, a negative regulator of gene expression. Development 126 : 4235–4245
Swarup R, Parry G, Graham N, Allen T, Bennett M (2002) Auxin cross-talk: integration of signalling pathways to control plant development. Plant Mol Biol 49 : 411–426
Tian Q, Reed JW (1999) Control of auxin-regulated root development by the Arabidopsis thaliana SH Y2/IAA3 gene. Development 126 : 711–721
Tian Q, Reed JW (2001) Molecular links between light and auxin signaling pathways. J Plant Growth Regul 20 : 274–280
Tian Q, Uhlir NJ, Reed JW (2002) Arabidopsis SHY2/IAA3 inhibits auxin-regulated gene expression. Plant Cell 14 : 301–319
Ursin VM, Bradford KJ (1989) Auxin and ethylene regulation of petiole epinasty in 2 developmental mutants of tomato, diageotropica and epinastic. Plant Physiol 90 : 1341–1346
Vandenbussche F, Smalle J, Le J, Madeira-Saibo NJ, De Paepe A, Chaerle L, Tietz O, Smets R, Laarhoven LJJ, Harren FJM et al. (2003) The Arabidopsis thaliana mutant alh1 illustrates a cross-talk between ethylene and auxin. Plant Physiol 131: 1228–1238
Vogel JP, Woeste KE, Theologis A, Kieber JJ (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
Watahiki M-K, Yamamoto K-T (1997) The massugu1 mutation of Arabidopsis identified with failure of auxin-induced growth curvature of hypocotyl confers auxin insensitivity to hypocotyl and leaf. Plant Physiol 115 : 419–426
Wheeler RM, White RG, Salisbury FB (1986) Gravitropsim in higher plant shoots: IV. Further studies on participation of ethylene Plant Physiol 82 : 534–542
Wullschleger SD, Hanson PJ, Gunderson CA (1992) Assessing the influence of exogenous ethylene on electron-transport and fluorescence quenching in leaves of Glycine max. Environ Exp Bot 32 : 449–455
Yamamoto KT, Mori H, Imaseki H (1992) CDNA cloning of indole-3-acetic acid-regulated genes: AUX22 and SAUR from mung bean (Vigna radiata) hypocotyl tissue. Plant Cell Physiol 33 : 93–97
Yang SF, Hoffman NE (1984) Ethylene biosynthesis and its regulation in higher plants. Ann Rev Plant Physiol 35 : 155–189
Yi HC, Joo S, Nam KH, Lee JS, Kang BG, Kim WT (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