Handbook of Plant and Crop Physiology

(Steven Felgate) #1

  1. D Feltkamp, R Masterson, J Starke, S Rosahl. Analysis of the involvement of ocs-like bZip-binding elements in
    the differential strength of the bidirectional mas1
    2
    promoter. Plant Physiol 105:259–268, 1994.

  2. E Lebel, P Heifetz, L Thorne, S Uknes, J Ryals, E Ward. Functional analysis of regulatory sequences control-
    lingPR-1gene expression in Arabidopsis. Plant J 16:223–233, 1998.

  3. J Rouster, R Leah, J Mundy, V Cameron-Mills. Identification of a methyl jasmonate–responsive region in the
    promoter of a lipoxygenase 1 gene in barley. Plant J 11:513–523, 1997.

  4. RS Friling, S Bergelson, V Daniel. Two adjacent AP-!–like binding sites form the electrophile-responsive ele-
    ment of the murine glutathione S-transferase Ya subunit gene. Proc Natl Acad Sci. U S A 89:668–672, 1992.

  5. J Ryals, U Neuenschwander, M Willitis, A Molina, H-Y Steiner, M Hunt. Systemic acquired resistance. Plant
    Cell 8:1809–1819, 1996.

  6. G Strompen, R Gruner, UM Pfitzner. An as-1–like motif controls the level of expression of the gene for the
    pathogenesis-related protein 1a from tobacco. Plant Mol Biol 37:871–883, 1998.

  7. Y Zhang, W Fan, M Kinkema, X Li, X Dong. Interaction of NPR1 with basic leucine zipper protein transcrip-
    tion factors that bind sequences required for salicylic acid induction of the PR-1gene. Proc Natl Acad Sci U S
    A 96:6522–6528, 1999.

  8. G Sessa, Y Meller, R Fluhr. A GCC element and G-box motif participate in ethylene-induced expression of the
    PRB-1bgene. Plant Mol Biol 28:145–153, 1995.

  9. T Neuefeind, P Reinemer, B Bieseler. Plant glutathione S-transferases and herbicide detoxification. Biol Chem
    378:199–205, 1997.

  10. DP Dixon, I Cummins, DJ Cole, R Edwards. Glutathione-mediated detoxification systems in plants. Curr Opin
    Plant Biol 1:258–266, 1998.

  11. K Marrs. The functions and regulation of glutathione S-transferases in plants. Annu Rev Plant Physiol Plant Mol
    Biol 47:127–158, 1996.

  12. BJ van der Zaal, FNJ Droog, FJ Pieterse, PJJ Hooykaas. Auxin-sensitive elements from promoters of tobacco
    GST genes and a consensus as-1–like element differ only in relative strength. Plant Physiol 110:79–88, 1996.

  13. Y Takahashi, T Nagata. parB: an auxin-regulated gene encoding glutathione S-transferase. Proc Natl Acad Sci
    U S A 89:56–59, 1992.

  14. Y Takahashi, H Kuroda, T Tanaka, I Takebe, T Nagata. Isolation of an auxin-regulated gene cDNA expressed
    during the transition from G 0 to S phase in tobacco mesophyll protoplasts. Proc Natl Acad Sci U S A
    86:9279–9283, 1989.

  15. Y Takahashi, M Kusaba, Y Hiraoka, T Nagata. Characterization of the auxin-regulated pargene from tobacco
    mesophyll protoplasts. Plant J 1:327–332, 1991.

  16. Y Takahashi, Y Niwa, Y Machida, T Nagata. Location of the cis-acting auxin-responsive region in the promoter
    of the pargene from tobacco mesophyll protoplasts. Proc Natl Acad Sci U S A 87:8013–8016, 1990.

  17. W Chen, G Chao, KB Singh. The promoter of a H 2 O 2 -inducible,ArabidopsisglutathioneS-transferase gene con-
    tains closely linked OBF- and OBP1-binding sites. Plant J 10:955–966, 1996.

  18. W Chen, KB Singh. The auxin, hydrogen peroxide and salicylic acid induced expression of the arabidopsis
    GST6 promoter is mediated in part by an ocs element. Plant J 19:667–677, 1999.

  19. MJ May, CJ Leaver. Arabidopsis thaliana -glutamylcysteine synthetase is structurally unrelated to mam-
    malian, yeast, and Escherichia colihomologues. Proc Natl Acad Sci U S A 91:10059–10063, 1995.

  20. C Wang, DJ Oliver. Cloning of the cDNA and genomic clones for glutathione synthetase from Arabidopsis
    thalianaand complementation of a gsh2 mutant in fission yeast. Plant Mol Biol 31:1093–1104, 1996.

  21. G Noctor, CH Foyer. Ascorbate and glutathione: keeping active oxygen under control. Annu Rev Plant Physiol
    Plant Mol Biol 49:249–279, 1998.

  22. E Grill, EL Winnacker, MH Zenk. Phytochelatins, a class of heavy-metal-binding peptides from plants, are func-
    tionally analogous to metallothioneins. Proc Natl Acad Sci U S A 84:439–443, 1987.

  23. C Xiang, DJ Oliver. Glutathione metabolic genes coordinately respond to heavy metals and jasmonic acid in
    Arabidopsis. Plant Cell 10:1539–1550, 1998.

  24. ZH Miao, X Liu, E Lam. TGA3is a distinct member of the TGA family of bZIP transcription factor in Ara-
    bidopsis thaliana. Plant Mol Biol 29:1–11, 1994.

  25. H Fromm, F Katagiri, N-H Chua. The tobacco transcription activator TGA1a binds to a sequence in the 5 up-
    stream region of a gene encoding a TGA1a-related protein. Mol Gen Genet 229:181–188, 1991.

  26. RA Creelman, ML Tierney, JE Mullet. Jasmonic acid/methyl jasmonate accumulate in wounded soybean
    hypocotyls and modulate wound gene expression. Proc Natl Acad Sci U S A 89:4938–4941, 1992.

  27. EE Farmer, CA Ryan. Interplant communication: airborne methyl jasmonate induces synthesis of proteinase in-
    hibitors in plant leaves. Proc Natl Acad Sci U S A 87:7713–7716, 1990.

  28. H Gundlach, MJ Muller, TM Kutchan, MH Zenk. Jasmonic acid is a signal transducer in elicitor-induced plant
    cell cultures. Proc Natl Acad Sci U S A 89:2389–2393, 1992.

  29. E Bell, JE Mullet. Lipoxygenase gene expression is modulated in plants by water deficit, wounding, and methyl
    jasmonate. Mol Gen Genet 230:456–462, 1991.

  30. I Anderson, W Becker, K Schluter, J Burges, B Parthier, K Apel. The identification of leaf thionin as one of the
    main jasmonate-induced proteins of barley. Plant Mol Biol 19:193–204, 1992.

  31. B Chaudhry, F Muller-Uri, V Cameron-Mills, S Gough, D Simpson, K Skriver, J Mundy. The barley 60 kDa
    jasmonate-induced protein (JIP60) is a novel ribosome-inactivating protein. Plant J 6:815–824, 1994.


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