Log in

Roles of plastid ε-3 fatty acid desaturases in defense response of higher plants

  • Minireview
  • Published:
Journal of Plant Research Aims and scope Submit manuscript

Abstract

In higher plants, the membrane lipids contain a high proportion of trienoic fatty acids. It has been suggested that these fatty acids, especially linolenic acid, play an important role as a precursor to a defense-related signal molecule, jasmonate. In Arabidopsis, three genes encoding the ε-3 fatty acid desaturase, namely, FAD3, FAD7 and FAD8, are responsible for the production of trienoic fatty acids. TheFAD3 enzyme is localized in microsomes, while theFAD7 and theFAD8 enzymes are localized in plastid membranes. Environmental stimuli, such as wounding, salt stress and pathogen invasion, which lead to a rapid increase in jasmonate production, significantly induce expression of theFAD7 andFAD8 genes. Recent findings have supported the view that plastids are involved in jasmonate production. We have been able to clarify the regulatory mechanism of a plastid ε-3 desaturase gene by analyzing the ArabidopsisFAD7 promoter with respect to tissue-specific, light-responsive and wound-induced expression. In particular, this promoter provides a unique model for studying the mechanism of transcriptional activation through wound signal transduction pathways.

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

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price includes VAT (Germany)

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Arondel, V., Lemieux, B., Hwang, I., Gibson, S., Goodman, H.M. andSomerville, C.R. 1992. Map-based cloning of a gene controlling omega-3 fatty acid desaturation inArabidopsis. Science258: 1353–1355.

    Article  PubMed  CAS  Google Scholar 

  • Berberich, T., Harada, M., Sugawara, K., Kodama, H., Iba, K. andKusano, T. 1998. Two maize genes encoding ω-3 fatty acid desaturase and their differential expression to temperature. Plant Mol Biol.36: 297–306.

    Article  PubMed  CAS  Google Scholar 

  • Blée, E. andJoyard, J. 1996. Envelope membranes from spinach chloroplasts are a site of metabolism of fatty acid hydroperoxides. Plant Physiol.110: 445–454.

    PubMed  Google Scholar 

  • Bowsher, C.G., Ferrie, B.J., Ghosh, S., Todd, J., Thompson, J.E. andRothstein, S.J. 1992. Purification and partial characterization of a membrane-associated lipoxygenase in tomato fruit. Plant Physiol.100: 1802–1807.

    PubMed  CAS  Google Scholar 

  • Browse, J., McCourt, P. andSomerville, C. 1986. A mutant of Arabidopsis deficient in C18∶3 and C16∶3 leaf lipids. Plant Physiol.81: 859–864.

    PubMed  CAS  Google Scholar 

  • Buell, C.R. andSomerville, C. 1995. Expression of defense-related and putative signaling genes during tolerant and susceptible interactions of Arabidopsis withXanthomonas campestris pv.campestris. Mol. Plant-Microbe Interact.8: 435–443.

    CAS  Google Scholar 

  • Creelman, R.A. andMullet, J.E. 1995. Jasmonic acid distribution and action in plants: Regulation during development and response to biotic and abiotic stress. Proc. Natl. Acad. Sci. USA92: 4114–4119.

    Article  PubMed  CAS  Google Scholar 

  • Creelman, R.A., Tierney, M.L. andMullet, J.E. 1992. Jasmonic acid/methyl jasmonate accumulate in wounded soybean hypocotyls and modulated wound gene expression. Proc. Natl. Acad. Sci. USA89: 4938–4941.

    Article  PubMed  CAS  Google Scholar 

  • Farmer, E.E. 1994. Fatty acid signaling in plants and their associated microorganisms. Plant Mol. Biol.26: 1423–1437.

    Article  PubMed  CAS  Google Scholar 

  • Farmer, E.E. andRyan, C.A. 1992. Octadecanoid precursors of jasmonic acid activate the synthesis of wound-inducible proteinase inhibitors. Plant Cell4: 129–134.

    Article  PubMed  CAS  Google Scholar 

  • Gibson, S., Arondel, V., Iba, K. andSomerville, C. 1994. Cloning of a temperature-regulated gene encoding a chloroplast ω-3 desaturase fromArabidopsis thaliana. Plant Physiol.106: 1615–1621.

    Article  PubMed  CAS  Google Scholar 

  • Gilmartin, P.M., Sarokin, L, Memelink, J. andChua, N.-H. 1990. Molecular light switches for plant genes. Plant Cell2: 369–378.

    Article  PubMed  CAS  Google Scholar 

  • Goldsbrough, A.P., Albrecht, H. andStratford, R. 1993. Salicylic acid-inducible binding of a tobacco nuclear protein to a 10 bp sequence which is highly conserved amongst stress-inducible genes. Plant J.3: 563–571.

    Article  PubMed  CAS  Google Scholar 

  • Hamada, T., Kodama, H., Nishimura, M. andIba, K. 1994. Cloning of a cDNA encoding tobacco ω-3 fatty acid desaturase. Gene147: 293–294.

    Article  PubMed  CAS  Google Scholar 

  • Hamada, T., Nishiuchi, T., Kodama, H., Nishimura, M. andIba, K. 1996. cDNA cloning of a wounding-inducible gene encoding a plastid ω-3 fatty acid desaturase from tobacco. Plant Cell Physiol.37: 606–611.

    PubMed  CAS  Google Scholar 

  • Horiguchi, G., Kawakami, N., Kusumi, K., Kodama, K. andIba, K. 1998. Developmental regulation of genes for microsome and plastid ω-3 fatty acid desaturases in wheat (Triticum aestivum L.). Plant Cell Physiol.39: 540–544.

    CAS  Google Scholar 

  • Iba, K., Gibson, S., Nishiuchi, T., Fuse, T., Nishimura, M., Arondel, V., Hugly, S. andSomerville, C. 1993. A gene encoding a chloroplast ω-3 fatty acid desaturase complements alterations in fatty acid desaturation and chloroplast copy number of the fad7 mutant ofArabidopsis thaliana. J. Biol. Chem.268: 24099–24105.

    PubMed  CAS  Google Scholar 

  • Kirsch, C., Takamiya-Wik, M., Reinold, S., Hahlbrock, K. andSomssich, I.E. 1997. Rapid, transient, and highly localized induction of the plastidial ω-3 fatty acid desaturase mRNA at fungal infection sites inPetroselinum crispum. Proc. Natl. Acad. Sci. USA94: 2079–2084.

    Article  PubMed  CAS  Google Scholar 

  • Kodama, H., Hamada, T., Horiguchi, G., Nishimura, M. andIba, K. 1994. Genetic enhancement of cold tolerance by expression of a gene for chloroplast ω-3 fatty acid desaturase in transgenic tobacco. Plant Physiol.105: 601–605.

    PubMed  CAS  Google Scholar 

  • Kodama, H., Horiguchi, G., Nishiuchi, T., Nishimura, M. andIba, K. 1995. Fatty acid desaturation during chilling acclimation is one of the factors involved in conferring low-temperature tolerance to young tobacco leaves. Plant Physiol.107: 1177–1185.

    PubMed  CAS  Google Scholar 

  • Kodama, H., Akagi, H., Kusumi, K., Fujimura, T. andIba, K. 1997. Structure, chromosomal location and expression of a rice gene encoding the microsome ω-3 fatty acid desaturase. Plant Mol. Biol.33: 493–502.

    Article  PubMed  CAS  Google Scholar 

  • Lemieux, B., Miquel, M., Somerville, C. andBrowse, J. 1990. Mutants ofArabidopsis with alterations in seed lipid fatty acid composition. Theor. Appl. Genet.80: 234–240.

    Article  CAS  Google Scholar 

  • McConn, M. andBrowse, J. 1996. The critical requirement for linolenic acid is pollen development, not photosynthesis, in an Arabidopsis mutant. Plant Cell8: 403–416.

    Article  PubMed  CAS  Google Scholar 

  • McConn, M., Hugly, S., Browse, J. andSomerville, C. 1994. A mutation at the fad8 locus of Arabidopsis identifies a second chloroplast ω-3 desaturase. Plant Physiol.106: 1609–1614.

    PubMed  CAS  Google Scholar 

  • McConn, M., Creelman, R.A., Bell, E., Mullet, J.E. andBrowse, J. 1997. Jasmonate is essential for insect defense inArabidopsis. Proc. Natl. Acad. Sci. USA94: 5473–5477.

    Article  PubMed  CAS  Google Scholar 

  • McCourt, P., Kunst, L., Browse, J. andSomerville, C.R. 1987. The effect of reduced amounts of lipid unsaturation on chloroplast ultrastructure and photosynthesis in a mutant ofArabidopsis. Plant Physiol84: 353–360.

    PubMed  CAS  Google Scholar 

  • Moons, A., Prinsen, E., Bauw, G. andVan Montagu, M. 1997. Antagonistic effects of abscisic acid and jasmonates on salt stress inducible transcripts in rice roots. Plant Cell9: 2243–2259.

    Article  PubMed  CAS  Google Scholar 

  • Mueller, M.J., Brodschelm, W., Spannagl, E. andZenk, M.H. 1993. Signaling in the elicitation process is mediated through the octadecanoid pathway leading to jasmonic acid. Proc. Natl. Acad. Sci. USA90: 7490–7494.

    Article  PubMed  CAS  Google Scholar 

  • Nishiuchi, T., Nishimura, M., Arondel, V. andIba, K. 1994. Genomic nucleotide sequence of a gene encoding a microsomal ω-3 fatty acid desaturase fromArabidopsis thaliana. Plant Physiol.105: 767–768.

    Article  PubMed  CAS  Google Scholar 

  • Nishiuchi, T., Nakamura, T., Abe, T., Kodama, H., Nishimura, M. andIba, K. 1995. Tissue-specific and light-responsive regulation of the promoter region of theArabidopsis thaliana chloroplast ω-3 fatty acid desaturase gene (FAD7). Plant Mol. Biol.29: 599–609.

    Article  PubMed  CAS  Google Scholar 

  • Nishiuchi, T., Hamada, T., Kodama, H. andIba, K. (1997). Wounding changes the spatial expression pattern of the Arabidopsis plastid ω-3 fatty acid desaturase gene (FAD7) through different signal transduction pathways. Plant Cell9: 1701–1712.

    Article  PubMed  CAS  Google Scholar 

  • Peña-Cortés, H., Albrecht, T., Prat, S., Weiler, E.W. andWillmitzer, L. 1993. Aspirin prevents wound-induced gene expression in tomato leaves by blocking jasmonic acid biosynthesis. Planta191: 123–128.

    Article  Google Scholar 

  • Rushton, P.J., Torres, J.T., Parniske, M., Wernert, P., Hahlbrock, K. andSomssich, I.E. 1996. Interaction of elicitor-induced DNA-binding proteins with elicitor response elements in the promoters of parsley PR1 genes. EMBO J.15: 5690–5700.

    PubMed  CAS  Google Scholar 

  • Somerville, C. andBrowse, J. 1991. Plant lipids: Metabolism, mutants, and membranes. Science252: 80–87.

    Article  CAS  PubMed  Google Scholar 

  • Thompson, W.F. andWhite, M.J. 1991. Physiological and molecular studies of light-regulated nuclear genes in higher plants, Annu. Rev. Plant Physiol. Plant Mol. Biol.42: 423–466.

    Article  CAS  Google Scholar 

  • Todoroki, S., Hayashi, T., Nagata, T., Kanegae, H., Mori, M. andKikuchi, S. 1998. cDNA cloning of gamma-ray inducible genes encoding ω-3 fatty acid desaturase from potato tuber. Plant Cell Physiol.39: S136.

    Google Scholar 

  • Vick, B.A. andZimmerman, D.C. 1984. Biosynthesis of jasmonic acid by several plant species. Plant Physiol.75: 458–461.

    Article  PubMed  CAS  Google Scholar 

  • Weber, H., Vick, B.A. andFarmer, E.E. 1997. Dinor-oxophytodienoic acid: A new hexadecanoid signal in the jasmonate family. Proc. Natl. Acad. Sci. USA94: 10473–10478.

    Article  PubMed  CAS  Google Scholar 

  • Yadav, N.S., Wierzbicki, A., Aegerter, M., Caster, C.S., Pérez-Grau, L., Kinney, A.J., Hitz, W.D., Booth, J.R., Jr., Schweiger, B., Stecca, K.L., Allen, S.M., Blackwell, M., Reiter, R.S., Carlson, T.J., Russell, S.H., Feldmann, K.A., Pierce, J. andBrowse, J. 1993. Cloning of higher plant ω-3 fatty acid desaturases. Plant Physiol.103: 467–476.

    Article  PubMed  CAS  Google Scholar 

  • Yamamoto, K.T., Mori, H. andImaseki, H. 1992 Novel mRNA sequences induced by indole 3 acetic acid in sections of elongating hypocotyls of mung bean (Vigna radiata). Plant Cell Physiol.33: 13–20.

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Koh Iba.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nishiuchi, T., Iba, K. Roles of plastid ε-3 fatty acid desaturases in defense response of higher plants. J. Plant Res. 111, 481–486 (1998). https://doi.org/10.1007/BF02507782

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02507782

Key words

Navigation