Skip to main content
PMC home page
The Plant Cell logoLink to The Plant Cell
. 1994 Sep;6(9):1197–1209. doi: 10.1105/tpc.6.9.1197

JIPs and RIPs: the regulation of plant gene expression by jasmonates in response to environmental cues and pathogens.

S Reinbothe 1, B Mollenhauer 1, C Reinbothe 1
PMCID: PMC160513  PMID: 7919988

Full Text

The Full Text of this article is available as a PDF (2.2 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Andresen I., Becker W., Schlüter K., Burges J., Parthier B., Apel K. The identification of leaf thionin as one of the main jasmonate-induced proteins of barley (Hordeum vulgare). Plant Mol Biol. 1992 May;19(2):193–204. doi: 10.1007/BF00027341. [DOI] [PubMed] [Google Scholar]
  2. Apuya N. R., Zimmerman J. L. Heat Shock Gene Expression Is Controlled Primarily at the Translational Level in Carrot Cells and Somatic Embryos. Plant Cell. 1992 Jun;4(6):657–665. doi: 10.1105/tpc.4.6.657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Baker T. C., Nishida R., Roelofs W. L. Close-range attraction of female oriental fruit moths to herbal scent of male hairpencils. Science. 1981 Dec 18;214(4527):1359–1361. doi: 10.1126/science.214.4527.1359. [DOI] [PubMed] [Google Scholar]
  4. Bartholomew D. M., Bartley G. E., Scolnik P. A. Abscisic Acid Control of rbcS and cab Transcription in Tomato Leaves. Plant Physiol. 1991 May;96(1):291–296. doi: 10.1104/pp.96.1.291. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bass H. W., Webster C., OBrian G. R., Roberts J. K., Boston R. S. A maize ribosome-inactivating protein is controlled by the transcriptional activator Opaque-2. Plant Cell. 1992 Feb;4(2):225–234. doi: 10.1105/tpc.4.2.225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Becker W., Apel K. Isolation and characterization of a cDNA clone encoding a novel jasmonate-induced protein of barley (Hordeum vulgare L.). Plant Mol Biol. 1992 Sep;19(6):1065–1067. doi: 10.1007/BF00040538. [DOI] [PubMed] [Google Scholar]
  7. Bednarek S. Y., Raikhel N. V. Intracellular trafficking of secretory proteins. Plant Mol Biol. 1992 Oct;20(1):133–150. doi: 10.1007/BF00029156. [DOI] [PubMed] [Google Scholar]
  8. Bell E., Mullet J. E. Lipoxygenase gene expression is modulated in plants by water deficit, wounding, and methyl jasmonate. Mol Gen Genet. 1991 Dec;230(3):456–462. doi: 10.1007/BF00280303. [DOI] [PubMed] [Google Scholar]
  9. Benatti L., Saccardo M. B., Dani M., Nitti G., Sassano M., Lorenzetti R., Lappi D. A., Soria M. Nucleotide sequence of cDNA coding for saporin-6, a type-1 ribosome-inactivating protein from Saponaria officinalis. Eur J Biochem. 1989 Aug 1;183(2):465–470. doi: 10.1111/j.1432-1033.1989.tb14951.x. [DOI] [PubMed] [Google Scholar]
  10. Bradley D. J., Kjellbom P., Lamb C. J. Elicitor- and wound-induced oxidative cross-linking of a proline-rich plant cell wall protein: a novel, rapid defense response. Cell. 1992 Jul 10;70(1):21–30. doi: 10.1016/0092-8674(92)90530-p. [DOI] [PubMed] [Google Scholar]
  11. Bunge S., Wolters J., Apel K. A comparison of leaf thionin sequences of barley cultivars and wild barley species. Mol Gen Genet. 1992 Feb;231(3):460–468. doi: 10.1007/BF00292716. [DOI] [PubMed] [Google Scholar]
  12. Calderwood S. B., Auclair F., Donohue-Rolfe A., Keusch G. T., Mekalanos J. J. Nucleotide sequence of the Shiga-like toxin genes of Escherichia coli. Proc Natl Acad Sci U S A. 1987 Jul;84(13):4364–4368. doi: 10.1073/pnas.84.13.4364. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Creelman R. A., Mullet J. E. Abscisic Acid accumulates at positive turgor potential in excised soybean seedling growing zones. Plant Physiol. 1991 Apr;95(4):1209–1213. doi: 10.1104/pp.95.4.1209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Creelman R. A., Mullet J. E. Water deficit modulates gene expression in growing zones of soybean seedlings. Analysis of differentially expressed cDNAs, a new beta-tubulin gene, and expression of genes encoding cell wall proteins. Plant Mol Biol. 1991 Oct;17(4):591–608. doi: 10.1007/BF00037046. [DOI] [PubMed] [Google Scholar]
  15. Crosby J. S., Vayda M. E. Stress-Induced Translational Control in Potato Tubers May Be Mediated by Polysome-Associated Proteins. Plant Cell. 1991 Sep;3(9):1013–1023. doi: 10.1105/tpc.3.9.1013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Daniels M. J., Barber C. E., Turner P. C., Sawczyc M. K., Byrde R. J., Fielding A. H. Cloning of genes involved in pathogenicity of Xanthomonas campestris pv. campestris using the broad host range cosmid pLAFR1. EMBO J. 1984 Dec 20;3(13):3323–3328. doi: 10.1002/j.1460-2075.1984.tb02298.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Dittrich H., Kutchan T. M., Zenk M. H. The jasmonate precursor, 12-oxo-phytodienoic acid, induces phytoalexin synthesis in Petroselinum crispum cell cultures. FEBS Lett. 1992 Aug 31;309(1):33–36. doi: 10.1016/0014-5793(92)80733-w. [DOI] [PubMed] [Google Scholar]
  18. Endo Y., Tsurugi K., Lambert J. M. The site of action of six different ribosome-inactivating proteins from plants on eukaryotic ribosomes: the RNA N-glycosidase activity of the proteins. Biochem Biophys Res Commun. 1988 Feb 15;150(3):1032–1036. doi: 10.1016/0006-291x(88)90733-4. [DOI] [PubMed] [Google Scholar]
  19. Enyedi A. J., Yalpani N., Silverman P., Raskin I. Signal molecules in systemic plant resistance to pathogens and pests. Cell. 1992 Sep 18;70(6):879–886. doi: 10.1016/0092-8674(92)90239-9. [DOI] [PubMed] [Google Scholar]
  20. Farmer E. E., Johnson R. R., Ryan C. A. Regulation of expression of proteinase inhibitor genes by methyl jasmonate and jasmonic Acid. Plant Physiol. 1992 Mar;98(3):995–1002. doi: 10.1104/pp.98.3.995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Farmer E. E., Ryan C. A. Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves. Proc Natl Acad Sci U S A. 1990 Oct;87(19):7713–7716. doi: 10.1073/pnas.87.19.7713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Farmer E. E., Ryan C. A. Octadecanoid Precursors of Jasmonic Acid Activate the Synthesis of Wound-Inducible Proteinase Inhibitors. Plant Cell. 1992 Feb;4(2):129–134. doi: 10.1105/tpc.4.2.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Franceschi V. R., Grimes H. D. Induction of soybean vegetative storage proteins and anthocyanins by low-level atmospheric methyl jasmonate. Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6745–6749. doi: 10.1073/pnas.88.15.6745. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Green T. R., Ryan C. A. Wound-Induced Proteinase Inhibitor in Plant Leaves: A Possible Defense Mechanism against Insects. Science. 1972 Feb 18;175(4023):776–777. doi: 10.1126/science.175.4023.776. [DOI] [PubMed] [Google Scholar]
  25. Gundlach H., Müller M. J., Kutchan T. M., Zenk M. H. Jasmonic acid is a signal transducer in elicitor-induced plant cell cultures. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2389–2393. doi: 10.1073/pnas.89.6.2389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Hattori T., Vasil V., Rosenkrans L., Hannah L. C., McCarty D. R., Vasil I. K. The Viviparous-1 gene and abscisic acid activate the C1 regulatory gene for anthocyanin biosynthesis during seed maturation in maize. Genes Dev. 1992 Apr;6(4):609–618. doi: 10.1101/gad.6.4.609. [DOI] [PubMed] [Google Scholar]
  27. Hildmann T., Ebneth M., Peña-Cortés H., Sánchez-Serrano J. J., Willmitzer L., Prat S. General roles of abscisic and jasmonic acids in gene activation as a result of mechanical wounding. Plant Cell. 1992 Sep;4(9):1157–1170. doi: 10.1105/tpc.4.9.1157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Katzin B. J., Collins E. J., Robertus J. D. Structure of ricin A-chain at 2.5 A. Proteins. 1991;10(3):251–259. doi: 10.1002/prot.340100309. [DOI] [PubMed] [Google Scholar]
  29. Kuhn D. N., Chappell J., Boudet A., Hahlbrock K. Induction of phenylalanine ammonia-lyase and 4-coumarate:CoA ligase mRNAs in cultured plant cells by UV light or fungal elicitor. Proc Natl Acad Sci U S A. 1984 Feb;81(4):1102–1106. doi: 10.1073/pnas.81.4.1102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Lamb C. J., Lawton M. A., Dron M., Dixon R. A. Signals and transduction mechanisms for activation of plant defenses against microbial attack. Cell. 1989 Jan 27;56(2):215–224. doi: 10.1016/0092-8674(89)90894-5. [DOI] [PubMed] [Google Scholar]
  31. Lamb F. I., Roberts L. M., Lord J. M. Nucleotide sequence of cloned cDNA coding for preproricin. Eur J Biochem. 1985 Apr 15;148(2):265–270. doi: 10.1111/j.1432-1033.1985.tb08834.x. [DOI] [PubMed] [Google Scholar]
  32. Larson D. E., Sells B. H. The function of proteins that interact with mRNA. Mol Cell Biochem. 1987 Mar;74(1):5–15. doi: 10.1007/BF00221907. [DOI] [PubMed] [Google Scholar]
  33. Marcotte W. R., Jr, Russell S. H., Quatrano R. S. Abscisic acid-responsive sequences from the em gene of wheat. Plant Cell. 1989 Oct;1(10):969–976. doi: 10.1105/tpc.1.10.969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Mason H. S., DeWald D. B., Mullet J. E. Identification of a methyl jasmonate-responsive domain in the soybean vspB promoter. Plant Cell. 1993 Mar;5(3):241–251. doi: 10.1105/tpc.5.3.241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Mason H. S., Dewald D. B., Creelman R. A., Mullet J. E. Coregulation of soybean vegetative storage protein gene expression by methyl jasmonate and soluble sugars. Plant Physiol. 1992 Mar;98(3):859–867. doi: 10.1104/pp.98.3.859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Mason H. S., Mullet J. E. Expression of two soybean vegetative storage protein genes during development and in response to water deficit, wounding, and jasmonic acid. Plant Cell. 1990 Jun;2(6):569–579. doi: 10.1105/tpc.2.6.569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. McGurl B., Pearce G., Orozco-Cardenas M., Ryan C. A. Structure, expression, and antisense inhibition of the systemin precursor gene. Science. 1992 Mar 20;255(5051):1570–1573. doi: 10.1126/science.1549783. [DOI] [PubMed] [Google Scholar]
  38. McGurl B., Ryan C. A. The organization of the prosystemin gene. Plant Mol Biol. 1992 Nov;20(3):405–409. doi: 10.1007/BF00040600. [DOI] [PubMed] [Google Scholar]
  39. Mueller M. J., Brodschelm W., Spannagl E., Zenk M. H. Signaling in the elicitation process is mediated through the octadecanoid pathway leading to jasmonic acid. Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7490–7494. doi: 10.1073/pnas.90.16.7490. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Nover L., Scharf K. D., Neumann D. Cytoplasmic heat shock granules are formed from precursor particles and are associated with a specific set of mRNAs. Mol Cell Biol. 1989 Mar;9(3):1298–1308. doi: 10.1128/mcb.9.3.1298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Nover L., Scharf K. D. Synthesis, modification and structural binding of heat-shock proteins in tomato cell cultures. Eur J Biochem. 1984 Mar 1;139(2):303–313. doi: 10.1111/j.1432-1033.1984.tb08008.x. [DOI] [PubMed] [Google Scholar]
  42. Pearce G., Strydom D., Johnson S., Ryan C. A. A polypeptide from tomato leaves induces wound-inducible proteinase inhibitor proteins. Science. 1991 Aug 23;253(5022):895–897. doi: 10.1126/science.253.5022.895. [DOI] [PubMed] [Google Scholar]
  43. Pēna-Cortés H., Sánchez-Serrano J. J., Mertens R., Willmitzer L., Prat S. Abscisic acid is involved in the wound-induced expression of the proteinase inhibitor II gene in potato and tomato. Proc Natl Acad Sci U S A. 1989 Dec;86(24):9851–9855. doi: 10.1073/pnas.86.24.9851. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Reimann-Philipp U., Schrader G., Martinoia E., Barkholt V., Apel K. Intracellular thionins of barley. A second group of leaf thionins closely related to but distinct from cell wall-bound thionins. J Biol Chem. 1989 May 25;264(15):8978–8984. [PubMed] [Google Scholar]
  45. Reinbothe S., Reinbothe C., Heintzen C., Seidenbecher C., Parthier B. A methyl jasmonate-induced shift in the length of the 5' untranslated region impairs translation of the plastid rbcL transcript in barley. EMBO J. 1993 Apr;12(4):1505–1512. doi: 10.1002/j.1460-2075.1993.tb05794.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Reinbothe S., Reinbothe C., Lehmann J., Becker W., Apel K., Parthier B. JIP60, a methyl jasmonate-induced ribosome-inactivating protein involved in plant stress reactions. Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7012–7016. doi: 10.1073/pnas.91.15.7012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Reinbothe S., Reinbothe C., Parthier B. Methyl jasmonate-regulated translation of nuclear-encoded chloroplast proteins in barley (Hordeum vulgare L. cv. salome). J Biol Chem. 1993 May 15;268(14):10606–10611. [PubMed] [Google Scholar]
  48. Ryder T. B., Cramer C. L., Bell J. N., Robbins M. P., Dixon R. A., Lamb C. J. Elicitor rapidly induces chalcone synthase mRNA in Phaseolus vulgaris cells at the onset of the phytoalexin defense response. Proc Natl Acad Sci U S A. 1984 Sep;81(18):5724–5728. doi: 10.1073/pnas.81.18.5724. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Scherrer K. Prosomes, subcomplexes of untranslated mRNP. Mol Biol Rep. 1990 Feb;14(1):1–9. doi: 10.1007/BF00422709. [DOI] [PubMed] [Google Scholar]
  50. Schindler U., Cashmore A. R. Photoregulated gene expression may involve ubiquitous DNA binding proteins. EMBO J. 1990 Nov;9(11):3415–3427. doi: 10.1002/j.1460-2075.1990.tb07549.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Staswick P. E. Jasmonate, genes, and fragrant signals. Plant Physiol. 1992 Jul;99(3):804–807. doi: 10.1104/pp.99.3.804. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Staswick P. E. Novel Regulation of Vegetative Storage Protein Genes. Plant Cell. 1990 Jan;2(1):1–6. doi: 10.1105/tpc.2.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Stirpe F., Bailey S., Miller S. P., Bodley J. W. Modification of ribosomal RNA by ribosome-inactivating proteins from plants. Nucleic Acids Res. 1988 Feb 25;16(4):1349–1357. doi: 10.1093/nar/16.4.1349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Stirpe F., Barbieri L. Ribosome-inactivating proteins up to date. FEBS Lett. 1986 Jan 20;195(1-2):1–8. doi: 10.1016/0014-5793(86)80118-1. [DOI] [PubMed] [Google Scholar]
  55. Tranbarger T. J., Franceschi V. R., Hildebrand D. F., Grimes H. D. The soybean 94-kilodalton vegetative storage protein is a lipoxygenase that is localized in paraveinal mesophyll cell vacuoles. Plant Cell. 1991 Sep;3(9):973–987. doi: 10.1105/tpc.3.9.973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Tsukaya H., Ohshima T., Naito S., Chino M., Komeda Y. Sugar-Dependent Expression of the CHS-A Gene for Chalcone Synthase from Petunia in Transgenic Arabidopsis. Plant Physiol. 1991 Dec;97(4):1414–1421. doi: 10.1104/pp.97.4.1414. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Vick B. A., Zimmerman D. C. Biosynthesis of jasmonic Acid by several plant species. Plant Physiol. 1984 Jun;75(2):458–461. doi: 10.1104/pp.75.2.458. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Wilen R. W., Mandel R. M., Pharis R. P., Holbrook L. A., Moloney M. M. Effects of Abscisic Acid and High Osmoticum on Storage Protein Gene Expression in Microspore Embryos of Brassica napus. Plant Physiol. 1990 Nov;94(3):875–881. doi: 10.1104/pp.94.3.875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Williams M. E., Foster R., Chua N. H. Sequences flanking the hexameric G-box core CACGTG affect the specificity of protein binding. Plant Cell. 1992 Apr;4(4):485–496. doi: 10.1105/tpc.4.4.485. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Williamson J. D., Quatrano R. S. ABA-Regulation of Two Classes of Embryo-Specific Sequences in Mature Wheat Embryos. Plant Physiol. 1988 Jan;86(1):208–215. doi: 10.1104/pp.86.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Plant Cell are provided here courtesy of Oxford University Press

RESOURCES