PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2005 | 47 | 1 |

Tytuł artykułu

Increased sensitivity to, and reduced production of, ethylene in a ABA-overproducing tomato mutant

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The single-gene male-sterile 7B-1 mutant in tomato (Lycopersicon esculentum Mill.) shows reduced de-etiolation of hypocotyl growth, has an elevated level of endogenous abscisic acid (ABA) and reduced amounts of growth-active gibberellins (GAs), is supersensitive to exogenous ABA, and is resistant to abiotic stresses in light but not in the dark. The existence of crosstalk between light signaling and plant hormones, and the interaction of ABA and GA biosynthetic pathways with ethylene, led us to investigate the possible role of ethylene in the 7B-1 mutant. In the dark, 7B-1 seedlings exhibited the normal triple response to 1-aminocyclopropane-l-carboxylic acid (ACC), an ethylene precursor, similar to the wild type. In light, however, hypocotyl growth of mutant seedlings was more sensitive to ACC but less sensitive to the inhibitors of ethylene’s action, such as silver thiosulfate, than the wild type. The 7B-1 mutant seedlings produced reduced levels of ethylene, which could account for the increased sensitivity to exogenous ACC. The mutant leaf discs also contained higher chlorophyll content and showed greater chlorophyll degradation in response to ACC than the wild type, and these could also be related to low ethylene production by the mutant. Fluridone, an inhibitor of ABA biosynthesis, countered the ACC-induced inhibition of hypocotyl elongation, and it also restored the wild-type phenotype in 7B-1 plants. The results suggest that the reduced de-etiolation of hypocotyl growth and the increased sensitivity of the mutant to ethylene in light are due to reduced ethylene production, which in turn may be related to high endogenous ABA. The data presented support our earlier findings that the 7B-1 mutant has a defect in light perception which affects both hormonal sensitivity and endogenous levels, thereby affecting hypocotyl and shoot growth.

Wydawca

-

Rocznik

Tom

47

Numer

1

Opis fizyczny

p.205-212,fig.,ref.

Twórcy

autor
  • University of Saskatchewan, 112 Science Place, Saskatoon, SK, S7N 5E2, Canada
autor
autor

Bibliografia

  • Abeles FB, Morgan PW, and Saltveit ME, JR. 1992. Ethylene in plant biology. Academic Press, San Diego.
  • Aharoni N. 1989. Interrelationship between ethylene and growth regulators in the senescence of lettuce leaf discs. Journal of Plant Growth Regulation 8: 309-317.
  • Beaudoin N, Serizet C, Gosti F, and Giraudat J. 2000. Interactions between abscisic acid and ethylene signaling cascades. Plant Cell 12: 1103-1115.
  • Davies PJ.1995. Plant hormones. Physiology, biochemistry and molecular biology. Kluwer Academic Publishers, Dordrecht.
  • Ecker J. 1995. The ethylene signal transduction pathways in plants. Science 268: 667-675.
  • Ephritikhine G, Fellner M, Vannini C, Lapous D, and Barbier-Brygoo H. 1999. The sax1 dwarf mutant of Arabidopsis thaliana shows altered sensitivity of growth responses to abscisic acid, auxin, gibberellins and ethylene and is partially rescued by exogenous brassinosteroid. Plant Journal 18: 303-314.
  • Fellner M, and Sawhney VK. 2001. Seed germination in a tomato male sterile mutant is resistant to osmotic, salt and low temperature stresses. Theoretical and Applied Genetics 102: 215-221.
  • Fellner M, and Sawhney VK. 2002. The 7B-1 mutant in tomato shows blue-light-specific resistance to osmotic stress and abscisic acid. Planta 214: 675-682.
  • Fellner M, Zhang R, Pharis RP, and Sawhney VK. 2001. Reduced de-etiolation of hypocotyl growth in a tomato mutant is associated with hypersensitivity to, and high endogenous levels, of abscisic acid. Journal of Experimental Botany 52: 725-738.
  • Finlayson SA, Lee IJ, and Morgan PW 1998. Phytochrome B and the regulation of circadian ethylene production in sorghum. Plant Physiology 116: 17-25.
  • Fluhr R, and Mattoo AK.1996. Ethylene - biosynthesis and perception. Critical Reviews in Plant Science 15: 479-523.
  • Gamble PE, and Mullet JE. 1986. Inhibition of carotenoid accumulation and abscisic acid biosynthesis in fluridone-treated dark-grown barley. European Journal of Biochemistry 160: 117-121.
  • Ghassemian M, Nambara E, Cutler S, Kawaide H, Kamiya Y, and McCourt P. 2000. Regulation of abscisic acid signaling by the ethylene response pathway in Arabidopsis. Plant Cell 12: 1117-1126.
  • Golan A, Tepper M, Soudry E, Horwitz B, and Gepstein S. 1996. Cytokinin, acting through ethylene, restores gravitropism to Arabidopsis seedlings grown in red light. Plant Physiology 112: 901-904.
  • Hansen H, and Grossmann K. 2000. Auxin-induced ethylene triggers abscisic acid biosynthesis and growth inhibition. Plant Physiology 124: 1437-1448.
  • Hooley R. 1994. Gibberellins: perception, transduction and responses. Plant Molecular Biology 26: 1529-1555.
  • Inskeep WP, and Bloom PR. 1985. Extinction coefficients of chlorophyll a and b in N,N-dimethylformamide and 80% acetone. Plant Physiology 77: 483-485.
  • Jackson MB. 1979. Is the diageotropica tomato ethylene deficient? Physiologia Plantarum 46: 347-351.
  • Jensen EB, and Veierskov B. 1998. Interaction between photoperiod, photosynthesis and ethylene formation in tomato plants (Lycopersicon esculentum cv. Ailsa Craig and ACC-oxidase antisense pTOM13). Physiologia Plantarum 103: 363-368 .
  • Kao CH, and Yang SF. 1982. Light inhibition of conversion of 1-aminocyclopropane carboxylic acid to ethylene in leaves is mediated through carbon dioxide. Planta 155: 261-266.
  • Kao CH, and Yang SF. 1983. Role of ethylene in the senescence of detached rice leaves. Plant Physiology 73: 881-885.
  • Khurana JP, Kochnar A, and Tyagi AK. 1998. Photosensory perception and signal transduction in higher plants - molecular genetic analysis. Critical Reviews in Plant Science 17: 465-539.
  • Kraepiel Y, and Miginiac E. 1997. Photomorphogenesis and phytohormones. Plant, Cell and Environment 20: 807-812.
  • Kumar PP, Lakshmanan P, and Thorpe TA. 1998. Regulation of morphogenesis in plant tissue culture by ethylene. In Vitro Cell and Developmental Biology - Plant 34: 94-103.
  • Murashige T, and Skoog A. 1962. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiologia Plantarum 15: 473-497.
  • Neff MM, Fankhauser C, and Chory J. 2000. Light: an indicator of time and place. Genes and Development 14: 257-271.
  • Neljubow DN. 1901. Über die horizontale mutation der stengel von Pisum sativum und einiger anderen. Pflanzen Beiträge und Botanik Zentralblatt 10: 128-139.
  • Noodén LD, and Leopold AC. 1988. Senescence and aging in plants. Academic Press, San Diego.
  • Pickett FB, Wilson AK, and Estelle M. 1990. The aux1 mutation of Arabidopsis confers both auxin and ethylene resistance. Plant Physiology 94: 1462-1466.
  • Pilet P-E, and Barlow PW. 1987. The role of abscisic acid in root growth and gravireaction: A critical review. Plant Growth Regulation 6: 217-265.
  • Reid DM, Beal FD, and Pharis RP. 1991. Environmental cues in plant development. In: Steward FC and Bidwell RGS [eds.], Plant physiology a treatise, vol. X, Growth and development, 65-181. Academic Press, New York.
  • Reid JB, and Howell SH. 1995. Hormone mutants and plant development. In: Davies PJ [ed.], Plant hormones. Physiology, biochemistry and molecular biology, 448-485. Kluwer Academic Publishers, Dordrecht.
  • Ross JJ, Murfet IC, and Reid JB. 1997. Gibberellin mutants. Physiologia Plantarum 100: 550-560.
  • Saab IN, Sharp RE, Pritchard J, and Voetberg GS. 1990. Increased endogenous abscisic acid maintains primary root growth and inhibits shoot growth of maize seedlings at low water potentials. Plant Physiology 93: 1329-1336.
  • Sawhney VK. 2004. Photoperiod-sensitive male-sterile mutant in tomato and its potential use in hybrid seed production. Journal of Horticultural Sciences and Biotechnology 79: 138-141.
  • Sharp RE, and Lenoble ME. 2002. ABA, ethylene and the control of shoot and root growth under water stress. Journal of Experimental Botany 53: 33-37.
  • Sharp RE, Lenoble ME, Else MA, Thorne ET, and Gherardi F. 2000. Endogenous ABA maintains shoot growth in tomato independently of effects on plant water balance: evidence for an interaction with ethylene. Journal of Experimental Botany 51: 1575-1584.
  • Shechter S, Goldschmidt EE, and Galili D. 1989. Persistence of [14C]gibberellin A3 and [3H]gibberellin A1 in senescing, ethylene treated citrus and tomato fruits. Plant Growth Regulation 8: 243-253.
  • Spollen WG, Lenoble ME, Samuels TD, Bernstein N, and Sharp RE. 2000. Abscisic acid accumulation maintains maize primary root elongation at low water potentials by restricting ethylene production. Plant Physiology 122: 967-976.
  • Thomas B, and Vince-Prue D. 1997. Photoperiodism in plants. Academic Press, San Diego, California.
  • Weckx J, and van Poucke M. 1989. The effect of white light on the ethylene biosynthesis of intact green seedlings. In: Clijsters H, de Proft M, Marcelle R, van Poucke M [eds.], Biochemical and physiological aspects of ethylene production in lower and higher plants, 279-290. Kluwer Academic Publishers, Dordrecht.
  • Wilson AK, Pickett FB, Turner JC, and Estelle M. 1990. A dominant mutation in Arabidopsis confers resistance to auxin, ethylene and abscisic acid. Molecular and General Genetics 222: 377-383.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-9d4fbef4-afff-4fcc-8350-c40354c47ca0
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.