Skip to main content
Log in

Wound and ethylene induction of the ACC oxidase melon gene CM-ACO1 occurs via two direct and independent transduction pathways

  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

The enzyme ACC oxidase catalyses the last step of ethylene biosynthesis in plants. Expression of the melon ACC oxidase gene, CM-ACO1, is rapidly induced (within 10 min) by ethylene treatment or upon wounding in leaves. The inhibitor of ethylene action, 1-methylcyclopropene (1-MCP), inhibited the accumulation of ethylene-induced CM-ACO1 mRNA transcripts, while wound-induced expression of the gene was not affected. The 5′-untranslated region of the CM-ACO1 gene was fused to the β-glucuronidase (GUS) reporter gene and the corresponding transgenic tobacco plants were analysed. Two separate regions of the CM-ACO1 promoter activated GUS expression in response to ethylene treatment and wounding. These results suggest that induction of CM-ACO1 gene expression occurs via two separate signal transduction pathways in response to wounding and ethylene treatment.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Abeles FB, Morgan PW, Salveit Jr ME: Ethylene in plant biology. Academic Press, San Diego (1992).

    Google Scholar 

  2. Balagué C, Watson CF, Turner AJ, Rougé P, Picton S, Pech JC, Grierson D: Isolation of a ripening and wound-induced cDNA from Cucumis melo L. encoding a protein with homology to the ethylene-forming enzyme. Eur J Biochem 212: 27–34 (1993).

    Google Scholar 

  3. Barry CS, Blume B, Bouzayen M, Cooper W, Hamilton AJ, Grierson D: Differential expression of the 1-aminocyclopropane-1-carboxylate oxidase gene family of tomato. Plant J 9: 525–535 (1996).

    Google Scholar 

  4. Boss PK, Gardner RC, Janssen BJ, Ross GS: An apple polyphenol oxidase cDNA is up-regulated in wounded tissues. Plant Mol Biol 27: 429–433 (1995).

    Google Scholar 

  5. Botella JR, Arteca RN, Frangos JA: A mechanical strain-induced 1-aminocyclopropane-1-carboxylic acid synthase gene. Proc Natl Acad Sci USA 92: 1595–1598 (1995).

    Google Scholar 

  6. Brederode FT, Linthorst HJM, Bol J: Differential induction of acquired resistance and PR gene expression in tobacco by virus infection, ethephon treatment, UV light and wounding. Plant Mol Biol 17: 1117–1125 (1991).

    Google Scholar 

  7. Callahan AM, Morgens PH, Wright P, Nichols KEJ: Comparison of Pch313 (pTOM 13 homolog) RNA accumulation during fruit softening and wounding of two phenotypically different peach cultivar. Plant Physiol 100: 482–488 (1992).

    Google Scholar 

  8. Davies KM, Grierson D: Identification of cDNA clones for tomato (Lycopersicum esculentum Mill.) mRNAs that accumulate during fruit ripening and leaf senescence in response to ethylene. Planta 179: 73–80 (1989).

    Google Scholar 

  9. Destefano-Beltran LJC, Van Caeneghem W, Richard L, Van Montagu M, Van der Straeten D: Characterization of three members of the ACC synthase gene family in Solanum tuberosum L. Mol Gen Genet 246: 496–508 (1995).

    Google Scholar 

  10. Diallinas G, Kanellis AK: A phenylalanine ammonia-lyase gene from melon fruit: cDNA cloning, sequence and expression in response to development and wounding. Plant Mol Biol 26: 473–479 (1994).

    Google Scholar 

  11. Dupille E, Rombaldi C, Lelievre JM, Cleyet-Marel JC, Pech JC, Latché A: Purification, properties and partial amino-acid sequence of 1-aminocyclopropane-1-carboxylic acid oxidase from apple fruits. Planta 190: 65–70 (1993).

    Google Scholar 

  12. Ecker JR, Davies RW: Plant defense genes are regulated by ethylene. Proc Natl Acad Sci USA 84: 5202–5206 (1987).

    Google Scholar 

  13. Eyal Y, Meller Y, Lev-Yadun S, Fluhr R: A basic-type PR-1 promoter directs ethylene responsiveness, vascular and abscission zone-specific expression. Plant J 4: 225–234 (1993).

    Google Scholar 

  14. Fluhr R, Mattoo AK: Ethylene: biosynthesis and perception. Crit Rev Plant Sci 15: 479–523 (1996).

    Google Scholar 

  15. Guis M, Bouquin T, Zegzouti H, Ayub R, Ben amor M, Lasserre E, Botondi R, Raynal J, Latché A, Bouzayen M, Balagué C, Pech JC: Differential expression of ACC oxidase genes in melon and physiological characterization of fruit expressing an antisense ACC oxidase gene. In: Kanellis AK, Chang C, Kende H, Grierson D (eds) Biology and Biotechnology of the Plant Hormone Ethylene, pp. 327–337. Kluwer Academic Publishers, Dordrecht, Netherlands (1997).

    Google Scholar 

  16. Holdsworth MJ, Schuch W, Grierson D: Nucleotide sequence of an ethylene-related gene from tomato. Nucl Acids Res 15: 10600 (1987).

    Google Scholar 

  17. Horvath DM, Chua N: Identification of an immediate-early salicilic acid-inducible tobacco gene and characterization of induction by others compounds. Plant Mol Biol 31: 1061–1072 (1996).

    Google Scholar 

  18. Itzhaki H, Woodson WR: Characterization of an ethylene-responsive glutathione S-transferase gene cluster in carnation. Plant Mol Biol 22: 43–58 (1993).

    Google Scholar 

  19. Kende H: Ethylene biosynthesis. Annu Rev Plant Physiol Plant Mol Biol 44: 283–307 (1993).

    Google Scholar 

  20. Kim WT, Yang SF: Structure and expression of cDNAs encoding 1-aminocyclopropane-1-carboxylate oxidase homologs isolated from excised mung bean hypocotyls. Planta 194: 223–229 (1994).

    Google Scholar 

  21. Kim JH, Kim WT, Kang BJ, Yang SF: Induction of 1-aminocyclopropane-1-carboxylate oxidase mRNAby ethylene in mung bean hypocotyls: involvement of both protein phos-phorylation and dephosphorilation in ethylene signaling. Plant J 11: 399–405 (1997).

    Google Scholar 

  22. Lasserre E, Bouquin T, Hernandez JA, Bull J, Pech JC, Balagué C: Structure and expression of three genes encoding ACC oxidase homologs from melon (Cucumis melo L.). Mol Gen Genet 251: 81–90 (1996).

    Google Scholar 

  23. Lasserre E, Godard F, Bouquin T, Hernandez JA, Pech JC, Roby D, Balagué C: Differential expression of two melon ACC oxidase gene promoters during plant development and pathogen attack. Mol Gen Genet, in press (1997).

  24. Liang X, Abel S, Keller JA, Shen NF, Theologis A: The 1-aminocyclopropane-1-carboxylate synthase gene family of Arabidopsis thaliana. Proc Natl Acad Sci USA 89: 11046– 11050 (1992).

    Google Scholar 

  25. Lincoln JE, Campbell AD, Oetiker J, Rottmann WH, Oeller PW, Shen NF, Theologis A: LE-ACS4, a fruit ripening and wound-induced 1-aminocyclopropane-1-carboxylate synthase gene of tomato (Lycopersicon esculentum). J Biol Chem 268: 19422–19430 (1993).

    Google Scholar 

  26. Liu D, Li N, Dube S, Kalinski A, Herman E, Mattoo AK: Molecular characterization of a rapidly and transiently wound-induced soybean (Glycine max L.) gene encoding 1-aminocyclopropane-1-carboxylate synthase. Plant Cell Physiol 34: 1151–1157 (1993).

    Google Scholar 

  27. Maxson JM, Woodson WR: Cloning of a DNA-binding protein that interacts with the ethylene-responsive enhancer element of the carnation GST1 gene. Plant Mol Biol 31: 751–759 (1996).

    Google Scholar 

  28. Miki T, Yamamoto M, Nakagawa H, Ogura N, Mori H, Imaseki H, Sato T: Nucleotide sequence of a cDNA for 1-aminocyclopropane-1-carboxylate synthase from melon fruits. Plant Physiol 107: 297–298 (1995).

    Google Scholar 

  29. Montgomery J, Goldman S, Deikman J, Margossian L, Fisher R: Identification of an ethylene-responsive region in the promoter of a fruit ripening gene. Proc Natl Acad Sci USA 90: 5939–5943 (1993).

    Google Scholar 

  30. Nakajima N, Nakagawa N, Imaseki H: Molecular size of wound-induced 1-aminocyclopropane-1-carboxylate synthase from Cucurbita maxima Duch. and change of translatable mRNA of the enzyme after wounding. Plant Cell Physiol 29: 989–998 (1988).

    Google Scholar 

  31. O'Donnell PJ, Calvert C, Atzorn R, Wasternack C, Leyser HMO, Bowles DJ: Ethylene as a signal mediating the wound response of tomato plants. Plant J 274: 1914–1917 (1996).

    Google Scholar 

  32. Ohme-Takagi M, Shinshi H: Ethylene-inducible DNA binding proteins that interact with an ethylene-responsive element. Plant J 7: 173–182 (1995).

    Google Scholar 

  33. Olson DC, Oetiker JH, Yang SF: Analysis of LE-ACO3, a 1-aminocyclopropane-1-carboxylic acid synthase gene expressed during flooding in the roots of tomato plant. J Biol Chem 270: 14056–14061 (1995).

    Google Scholar 

  34. Palm CJ, Costa MA, An G, Ryan CA: Wound-inducible nuclear protein binds DNA fragments that regulate a proteinase inhibitor II gene from potato. Proc Natl Acad Sci USA 87: 603–607 (1990).

    Google Scholar 

  35. Saarikoski P, Clapham D, von Arnold S: A wound-inducible gene from Salix viminalis coding for a trypsin inhibitor. Plant Mol Biol 31: 465–478 (1996).

    Google Scholar 

  36. Siebertz B, logemann J, Willmitzer L, Schell J: cis-Analysis of the wound-inducible promoter wun1 in transgenic tobacco plants and histochemical localization of its expression. Plant Cell 1: 961–968 (1989).

    Google Scholar 

  37. Sisler EC, Serek M, Dupille E: Comparison of cyclopropene,1-methylcyclopropene, and 3,3-dimethylcyclopropene as ethylene antagonists in plants. Plant Growth Regul 17: 1–6 (1995).

    Google Scholar 

  38. Spanu P, Boller T, Kende H: Differential accumulation of transcripts of 1-aminocyclopropane-1-carboxylate synthase genes in tomato plants infected with Phytophthora infestans and in elicitor-treated tomato cell suspensions. J Plant Physiol 141: 557–562 (1993).

    Google Scholar 

  39. Tang X, Gomes AMTR, Bhatia A, Woodson WR: Pistil-specific and ethylene-regulated expression of 1-aminocyclopropane-1-carboxylate oxidase genes in petunia flowers. Plant Cell 6: 1227–1239 (1994).

    Google Scholar 

  40. Xu R, Goldman S, Coupe S, Deikman J: Ethylene control of E4 transcription during tomato fruit ripening involves two cooperative cis element. Plant Mol Biol 31: 1117–1127 (1996).

    Google Scholar 

  41. Yang SF, Hoffman NE: Ethylene biosynthesis and its regulation in higher plants. Annu Rev Plant Physiol 35: 155–189 (1984).

    Google Scholar 

  42. Yip WK, Moore T, Yang SF: Differential accumulation of transcripts for four tomato 1-aminocyclopropane-1-carboxylate synthase homologs under various conditions. Proc Natl Acad Sci USA 89: 2475–2479 (1992).

    Google Scholar 

  43. Zarembinski TI, Theologis A: Ethylene biosynthesis and action: a case of conservation. Plant Mol Biol 26: 1579–1597 (1994).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bouquin, T., Lasserre, E., Pradier, J. et al. Wound and ethylene induction of the ACC oxidase melon gene CM-ACO1 occurs via two direct and independent transduction pathways. Plant Mol Biol 35, 1029–1035 (1997). https://doi.org/10.1023/A:1005902226054

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1005902226054

Navigation