Abstract
Transgenic tobacco plants (ppa-1) constitutively expressing Escherichia coli pyrophosphatase behind the 35S CaMV promoter accumulate high levels of soluble sugars in their leaves [27]. These plants were considered a tool to study adaptation of leaves to photoassimilate accumulation at the molecular level. By differential hybridization of a subtractive library enriched for transcripts present in the transgenic plants 12 different cDNAs were isolated. By sequence analysis four cDNAs could be identified as 1-aminocyclopropane-1-carboxylate-oxidase and as three different pathogenesis-related proteins (PR-1b, PR-Q and SAR 8.2). Two cDNAs were homologous to a calmodulin-like protein from Arabidopsis and a human ribosomal protein L19 while six cDNA clones remained unknown. One of these clones (termed PAR-1 for photoassimilate-responsive) displayed features similar to pathogenesis-related proteins: Hybridizing transcripts, 1.2 and 1.0 kb in length, were strongly inducible by salicylate and accumulated in tobacco plants after infection with potato virus Y (PVY) both in infected and uninfected systemic leaves. PAR-1 transcripts also accumulated in wildtype leaves upon floating on glucose and sucrose whereas sorbitol and polyethylene glycol had no effect. Rescreening of the ppa-1 cDNA library with the PAR-1 cDNA as probe resulted in 25 hybridizing cDNAs which by homology were found to fall into three classes (PAR-1a, b, c). The cDNAs coding for PAR-1a and b were 90.6% homologous on the DNA level while both were less related to the PAR-1c cDNA (70.5% and 75.2% homologous, respectively). One open reading frame was identified in all three PAR-1 cDNA classes. Translation would result in proteins with a theoretical molecular mass of about 20 kDa. The N-terminal amino acid sequences resemble a signal peptide which would direct the proteins to the secretory pathway. Using selective 3′ hybridization probes of the three PAR-1 cDNAs it was possible to discriminate the different transcripts. Both PAR-1a and PAR-1c mRNAs are induced in plants treated with PVY.
Key words: gene regulation, pathogenesis-related proteins, potato virus Y, subtractive cDNA library, sugar accumulation, transgenic tobacco plants
References
- 1.Amasino RM. Acceleration of nucleic acid hybridisation rate by polyethylene glykol. Anal Biochem. 1986;152:304–307. doi: 10.1016/0003-2697(86)90413-6. [DOI] [PubMed] [Google Scholar]
- 2.Bartling, EMBL data library, accession number X68054,
- 3.Brederode FT, Linthorst HJM, Bol JF. Differential induction of acquired resistance and PR gene expression in tobacco by virus infection, ethephon treatment, UV light and wounding. Plant Mol Biol. 1991;17:1117–1125. doi: 10.1007/BF00028729. [DOI] [PubMed] [Google Scholar]
- 4.Cornelissen BJC, van Huijsduijnen RAMH, van Loon LC, Bol JF. Molecular characterization of messenger RNAs for pathogenesis-related proteins 1a, 1b and 1c, induced by TMV infection of tobacco. EMBO J. 1986;5:37–40. doi: 10.1002/j.1460-2075.1986.tb04174.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Geigenberger P, Lerchl J, Stitt M, Sonnewald U: Phloem-specific expression of pyrophosphatase inhibits long distance transport of carbohydrates and amino acids in tobacco plants. Plant Cell Environ, in press.
- 6.Goldschmidt EE, Huber SC. Regulation of photosynthesis by end-product accumulation in leaves of plants storing starch, sucrose, and hexose sugars. Plant Physiol. 1992;99:1443–1448. doi: 10.1104/pp.99.4.1443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Holdsworth MJ, Bird CR, Ray J, Schuch W, Grierson D. Structure and expression of an ethylene-related mRNA from tomato. Nucl Acids Res. 1987;15:731–739. doi: 10.1093/nar/15.2.731. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Jang JC, Sheen J. Sugar sensing in higher plants. Plant Cell. 1994;6:1665–1679. doi: 10.1105/tpc.6.11.1665. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Jelitto T, Sonnewald U, Willmitzer L, Hajirezeai M, Stitt M. Inorganic pyrophosphate content and metabolites in potato and tobacco plants expressing E. coli pyrophosphatase in their cytosol. Planta. 1992;188:238–244. doi: 10.1007/BF00216819. [DOI] [PubMed] [Google Scholar]
- 10.Johnson R, Ryan CA. Wound-inducible potato inhibitor II genes: enhancement of expression by sucrose. Plant Mol Biol. 1990;14:527–536. doi: 10.1007/BF00027498. [DOI] [PubMed] [Google Scholar]
- 11.Kim SR, Costa MA, An G. Sugar response element enhances wound response of potato proteinase inhibitor II promoter in transgenic tobacco. Plant Mol Biol. 1991;17:973–983. doi: 10.1007/BF00037137. [DOI] [PubMed] [Google Scholar]
- 12.Krapp A, Hofmann B, Schäfer C, Stitt M. Regulation of the expression of rbcS and other photosynthetic genes by carbohydrates: a mechanism for the ‘sink regulation’ of photosynthesis? Plant J. 1993;3:817–828. [Google Scholar]
- 13.Krapp A, Quick WP, Stitt M. Ribulose-1,5-bisphosphate carboxylase-oxygenase, other photosynthetic enzymes and chlorophyll decrease when glucose is supplied to mature spinach leaves via the transpiration stream. Planta. 1991;186:58–69. doi: 10.1007/BF00201498. [DOI] [PubMed] [Google Scholar]
- 14.Kumabe T, Schma Y, Yamamoto T. Human cDNAs encoding elongation factor 1g and the ribosomal protein RL19. Nucl Acids Res. 1992;20:2598. doi: 10.1093/nar/20.10.2598. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Lerchl J, Geigenberger P, Stitt M, Sonnewald U. Impaired photoassimilate partitioning caused by phloem-specific pyrophosphate removal can be complemented by a phloem-specific cytosolic yeast-derived invertase in transgenic plants. Plant Cell. 1995;7:259–270. doi: 10.1105/tpc.7.3.259. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Logemann J, Schell J, Willmitzer L. Improved method for the isolation of RNA from plant tissues. Anal Biochem. 1987;163:21–26. doi: 10.1016/0003-2697(87)90086-8. [DOI] [PubMed] [Google Scholar]
- 17.Mönke G, Sonnewald U. Elevated mRNA levels of the ribosomal protein L19 and a calmodulin-like protein in assimilate accumulating transgenic tobacco plants. Plant Physiol. 1995;107:1451–1452. doi: 10.1104/pp.107.4.1451. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Ohashi Y, Matsuoka M. Synthesis of stress proteins in tobacco leaves. Plant Cell Physiol. 1985;26:473–480. [Google Scholar]
- 19.Ohashi Y, Ohshima M. Stress-induced expression of genes for pathogenesis-related proteins in plants. Plant Cell Physiol. 1992;33:819–826. [Google Scholar]
- 20.Payne G, Ahl P, Moyer M, Harper A, Beck J, Meins FJR, Ryals J. Isolation of complementary DNA clones encoding pathogenesis-related proteins P and Q, and acidic chitinases from tobacco. Proc Natl Acad Sci USA. 1990;87:98–102. doi: 10.1073/pnas.87.1.98. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Philosoph-Hadas S, Meir S, Aharoni N. Carbohydrates stimulate ethylene production in tobacco leaf discs. II. Sites of stimulation in the ethylene biosynthesis pathway. Plant Physiol. 1985;78:139–143. doi: 10.1104/pp.78.1.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Pierpoint WS, Robinson NP, Leason MB. The pathogenesis-related proteins in tobacco: Their induction by viruses in intact plants and their induction by chemicals in detached leaves. Physiol Plant Path. 1981;19:85–97. [Google Scholar]
- 23.Sambrook J, Fritsch EF, Maniatis T. Molecular Cloning: A Laboratory Manual. 2nd ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory; 1989. [Google Scholar]
- 24.Sheen J. Metabolic repression of transcription in higher plants. Plant Cell. 1990;2:1027–1038. doi: 10.1105/tpc.2.10.1027. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Singh NK, Bracker CA, Hasegawa PM, Handa AK, Bruckel S, Hermodson MA, Pfankoch E, Regnier FE, Bressan RA. Characterization of osmotin. Thaumatin-like protein associated with osmotic adaptation in plant cells. Plant Physiol. 1987;85:529–536. doi: 10.1104/pp.85.2.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Singh NK, Nelson DE, Kuhn D, Hasegawa PM, Bressan RA. Molecular cloning of osmotin and regulation of its expression by ABA and adaptation to low water potential. Plant Physiol. 1989;90:1096–1101. doi: 10.1104/pp.90.3.1096. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Sonnewald U. Expression of E. coli inorganic pyrophosphatase in transgenic plants alters photoassimilate partitioning. Plant J. 1992;2:571–581. [PubMed] [Google Scholar]
- 28.Sonnewald U, Wilke I, Herbers K: Plant responses to sugar accumulation in transgenic tobacco plants. In: Madore MA, Lucas WJ (eds) Carbon Partitioning and Source-Sink Interactions in Plants, pp. 246–257. American Society of Plant Physiologists (1995).
- 29.Steudel W, Heiling A: Die Vergilbungskrankheit der Rübe. Mitt Biol Zentralanst Land- Forstw Berlin-Dahlem, Heft 79 (1954).
- 30.Strauss D, Ausubel FM. Genomic subtraction for cloning DNA corresponding to deletion mutations. Proc Natl Acad Sci USA. 1990;87:1889–1893. doi: 10.1073/pnas.87.5.1889. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Sturm A, Chrispeels MJ. cDNA cloning of carrot extracellular β-fructosidase and its expression in response to wounding and bacterial infection. Plant Cell. 1990;2:1107–1119. doi: 10.1105/tpc.2.11.1107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Técsi LI, Maule AJ, Smith AM, Leegood RC. Complex, localized changes in CO2 assimilation and starch content associated with the susceptible interaction between cucumber mosaic virus and a cucurbit host. Plant J. 1994;5:837–847. [Google Scholar]
- 33.Tsukaya H, Oshima 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;97:1414–1421. doi: 10.1104/pp.97.4.1414. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.van Oosten JJ, Wilkins D, Besford RT. Regulation of the expression of photosynthetic nuclear genes by CO2 is mimicked by regulation by carbohydrates: a mechanism for the acclimation of photosynthesis to high CO2. Plant Cell Environ. 1994;17:913–923. [Google Scholar]
- 35.Ward ER, Uknes SJ, Williams SC, Dincher SS, Wiederhold DL, Alexander DC, Ahl-Goy P, Métraux J-P, Ryals A. Coordinate gene activity in response to agents that induce systemic aquired resistance. Plant Cell. 1991;3:1085–1094. doi: 10.1105/tpc.3.10.1085. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Watson MA, Watson DJ. The effect of infection with beet yellows and beet mosaic viruses on the carbohydrate content of sugar-beet leaves, and on translocation. Ann Appl Biol. 1951;38:276–288. [Google Scholar]