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cDNA cloning, substrate specificity and expression study of tobacco caffeoyl-CoA 3-O-methyltransferase, a lignin biosynthetic enzyme

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Abstract

Four caffeoyl-CoA 3-O-methyltransferase (CCoAOMT) cDNA clones were isolated from RNA extracted from TMV-infected tobacco leaves using an heterologous DNA probe. The cDNAs were 84–93% identical in their nucleotide sequences, indicating that they are the products of four closely related genes. A comparison of the CCoAOMT cDNAs with database sequences and Southern blot analysis indicated that they are encoded by a new CCoAOMT family of tobacco. Overall expression of this gene family in tobacco tissues was investigated by RNA blot analysis. The expression of each individual gene was studied by RT-PCR coupled with RFLP analysis of PCR products, taking advantage of the presence of specific restriction sites in each cloned cDNA. Two members of the CCoAOMT gene family appeared to be constitutively expressed in various plant organs and tissues whereas the two others were preferentially expressed in flower organs, after tobacco mosaic virus (TMV) infection or elicitor treatment of leaves. The CCoAOMT enzymatic protein expressed in bacteria was purified and shown to be specific for the caffeoyl-CoA and 5-hydroxyferuloyl-CoA esters and to have no activity against free caffeic acid and 5-hydroxyferulic acid. The pattern of CCoAOMT transcript accumulation during development of tobacco stem was found closely related to that of COMT I genes which have been shown to be specifically involved in lignin biosynthesis. Moreover, the inhibition of COMT I gene expression in transgenic tobacco was also shown to decrease CCoAOMT gene expression, particularly in the most lignified tissues. Thus, the expression pattern and the substrate specificity of tobacco CCoAOMT sustain a preferential role in lignin biosynthesis.

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References

  1. Atanassova R, Favet N, Martz F, Chabbert B, Thollier M-T, Monties B, Fritig B, Legrand M: Altered lignin composition in transgenic tobacco expressing O-methyltransferase sequences in sense and antisense orientation. Plant J 8: 465–477 (1995).

    Google Scholar 

  2. Becker-André M, Hahlbrock K: Absolute mRNA quantification using the polymerase chain reaction (PCR). A novel approach by a PCR aided transcript titration assay (PATTY). Nucl Acids Res 22: 9437–9446 (1989).

    Google Scholar 

  3. Boudet AM, Lapierre C, Grima-Pettenati J: Biochemistry and molecular biology of lignification. New Phytol 129: 203–236 (1995).

    Google Scholar 

  4. Campbell MM, Sederoff RR: Variation in lignin content and composition: mechanism of control and implications for the genetic improvement of plants. Plant Physiol 110: 3–13 (1996).

    PubMed  Google Scholar 

  5. Collendavelloo J, Legrand M, Geoffroy P, Barthelemy J, Fritig B: Purification and properties of the three o-diphenol Omethyltransferases of tobacco leaves. Phytochemistry 20: 611–616 (1981).

    Google Scholar 

  6. Fukasawa-Akada T, Kung S-D, Watson JC: Phenylalanine ammonia-lyase gene structure, expression, and evolution in Nicotiana. Plant Mol Biol 80: 711–722 (1996).

    Google Scholar 

  7. Geoffroy P, Legrand M, Fritig B: Isolation and characterization of a proteinaceous inhibitor of microbial proteinases induced during the hypersensitive reaction of tobacco to tobaccomosaic virus. Mol Plant-Microbe Interact 3: 327–333 (1990).

    PubMed  Google Scholar 

  8. Guan KL, Dixon JE: Eukaryotic proteins expressed in E. coli: an improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase. Anal Biochem 192: 262–267 (1991).

    PubMed  Google Scholar 

  9. Hermann C, Legrand M, Geoffroy P, Fritig B: Enzymatic synthesis of lignin: purification to homogeneity of the three O-methyltransferases of tobacco and production of specific antibodies. Arch Biochem Biophys 253: 367–376 (1987).

    PubMed  Google Scholar 

  10. Jaeck E, Dumas B, Geoffroy P, Favet N, Inzé D, Van Montagu M, Fritig B, Legrand M: Regulation of enzymes involved in lignin biosynthesis: induction of O-methyltransferase mRNAs during the hypersensitive reaction of tobacco to tobaccomosaic virus. Mol Plant-Microbe Interact 5: 294–300 (1992).

    PubMed  Google Scholar 

  11. Jaeck E, Martz F, Stiefel V, Fritig B, Legrand M: Expression of tobacco class I O-methyltransferase in healthy and TMV-infected tobacco. Mol Plant-Microbe Interact 9: 681–688 (1996).

    PubMed  Google Scholar 

  12. Kauffmann S, Baillieul F, Genetet I, Kopp M, Fritig B: Two proteins secreted by Phytophthora megasperma elicit necrosis and defence-related responses in tobacco. In: Fritig B, Legrand M (eds) Mechanisms of Plant Defence Responses, pp. 140–143. Kluwer Academic Publishers, Dordrecht, Netherlands (1993).

    Google Scholar 

  13. Kühnl T, Koch U, Heller W, Wellmann E: Elicitor induced Sadenosyl-L-methionine: caffeoyl-CoA 3-O-methyltransferase from carrot cell suspension cultures. Plant Sci 60: 21–25 (1989).

    Google Scholar 

  14. Lange BM, Lapierre C, Sandermann HJ: Elicitor-induced spruce stress lignin. Structural similarity to early developmental lignins. Plant Physiol 108: 1277–1287 (1995).

    PubMed  Google Scholar 

  15. Legrand M, Fritig B, Hirth L: o-diphenol O-methyltransferases of healthy and tobacco-mosaic-virus-infected hypersensitive tobacco. Planta 144: 101–108 (1978).

    Google Scholar 

  16. Lewis NG, Yamamoto E: Lignin: occurrence, biogenesis and biodegradation. Annu Rev Plant Physiol Plant Mol Biol 41: 455–496 (1990).

    PubMed  Google Scholar 

  17. Ni W, Sewalt JH, Korth KL, Blount JW, Ballance GM, Dixon RA: Stress responses in alfalfa. XXI. Activation of caffeic acid 3-O-methyltransferase and caffeoyl-coenzyme A 3-O-methyltransferase genes does not contribute to changes in metabolite accumulation in elicitor-treated cell-suspension cultures. Plant Physiol 112: 717–726 (1996).

    PubMed  Google Scholar 

  18. Pakusch A-E, Matern U, Schiltz E: Elicitor-inducible caffeoyl-Coenzyme A 3-O-methyltransferase from Petroselinum crispum cell suspensions. Plant Physiol 95: 137–143 (1991).

    Google Scholar 

  19. Pakusch A-E, Kneusel RE, Matern U: S-adenosyl-Lmethionine: trans-caffeoyl-coenzyme A 3-O-methyltransferase from elicitor-treated parsley cell suspension cultures. Arch Biochem Biophys 271: 488–494 (1989).

    PubMed  Google Scholar 

  20. Pellegrini LOG, Rohfritsch O, Fritig B, Legrand M: Phenylalanine ammonia-lyase in tobacco. Molecular cloning and gene expression during the hypersensitive reaction to tobacco mosaic virus and the response to a fungal elicitor. Plant Physiol 106: 877–886 (1994).

    PubMed  Google Scholar 

  21. Pellegrini LOG, Geoffroy P, Fritig B, Legrand M: Molecular cloning and expression of a new class of ortho-diphenol-O-methyltransferases induced in tobacco leaves by infection or elicitor treatment. Plant Physiol 103: 509–517 (1993).

    PubMed  Google Scholar 

  22. Rasmussen UB, Basset P, Daniel JY: Direct amplification of cDNA inserts from λ libraries using the cloning-adapter as primer for PCR. Nucl Acids Res 17: 3308 (1989).

    PubMed  Google Scholar 

  23. Ride JP: Cell wall and other structural barriers in defence. In: Callow JA (ed) Biochemical Plant Pathology, pp. 215–236. John Wiley, Chichester, UK (1983).

    Google Scholar 

  24. Sanger F, Nicklen S, Coklson AR: DNAsequencingwith chainterminating inhibitors. Proc Natl Acad Sci USA 74: 5463–5467 (1977).

    PubMed  Google Scholar 

  25. Schmitt D, Pakusch A-E, Matern U: Molecular cloning, induction, and taxonomic distribution of caffeoyl-CoA 3-Omethyltransferase, an enzyme involved in disease resistance. J Biol Chem 266: 17416–17423 (1991).

    PubMed  Google Scholar 

  26. Terashima N, Fukushima K: Biogenesis and structure of macromolecular lignin in the cell wall of tree xylem as studied by microautoradiography. In: Lewis NG, Paice MG (eds) Plant Cell Walls: Polymers, Biogenesis and Biodegradation, pp. 160–168. American Chemical Society Symposium Series 399, Washington, DC (1989).

    Google Scholar 

  27. Vance CP, Kirk TK, Sherwood RT: Lignification as a mechanism of disease resistance. Annu Rev Phytopath 18: 259–288 (1980).

    Google Scholar 

  28. Vidgren J, Svensson LA, Liljas A: Crystal structure of catecholO-methyltransferase. Nature 369: 354–358 (1994).

    Google Scholar 

  29. Ye Z-H, Kneusel RE, Matern U, Varner JE: An alternative methylation pathway in lignin biosynthesis in Zinnia. Plant Cell 6: 1427–1439 (1994).

    Article  PubMed  Google Scholar 

  30. Ye Z-H, Varner JE: Differential expression of two O-methyltransferases in lignin biosynthesis in Zinnia elegans. Plant Physiol 108: 459–467 (1995).

    PubMed  Google Scholar 

  31. Zhang X-H, Dickson EE, Chinnappa CC: Nucleotide sequence of a cDNA clone encoding caffeoyl-Coenzyme A 3-Omethyltransferase of Stellaria longipes (Caryophyllaceae). Plant Physiol 108: 429–430 (1995).

    PubMed  Google Scholar 

  32. Zou J, Taylor DC: Isolation of an Arabidopsis thaliana cDNA homologous to parsley (Petroselinum crispum) Sadenosyl-L-methionine: trans-caffeoyl-Coenzyme A 3-Omethyltransferase, an enzyme involved in disease resistance. Plant Physiol Biochem 32: 423–427 (1994).

    Google Scholar 

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Martz, F., Maury, S., Pinçon, G. et al. cDNA cloning, substrate specificity and expression study of tobacco caffeoyl-CoA 3-O-methyltransferase, a lignin biosynthetic enzyme. Plant Mol Biol 36, 427–437 (1998). https://doi.org/10.1023/A:1005969825070

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