Abstract
Many interactions between plants and their parasites begin with specific recognition. The nature of this recognition, and of subsequent signal transduction by both host and parasite have profound impact on the outcome of the interaction. Plants have evolved effective mechanisms to recognize pathogenic microbes and halt their biotrophic or necrotrophic growth. Active plant defense mechanisms obviously force adaptive selection for microbe variants which can evade the plant’s recognition capabilities. This evolutionary tug of war has led to a complex set of both plant and microbe genes whose interaction is required for a successful resistance reaction. As well as a potentially large array of recognition functions, a number of subsequent functions must exist which are necessary to establish a completely effective resistant phenotype.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Debener T, Lehnackers H, Arnold M, Dangl JL. Identification and molecular mapping of a single Arabidopsis thaliana locus determining resistance to a phytopathogenic Pseudomonas syringae isolate. Plant J. 1991;1:289–302.
Dangl JL, Ritter C, Gibbon MJ, et al. Functional homologs of the Arabidopsis RPM1 disease resistance gene in bean and pea. Plant Cell 1992;4:1359–1369.
Bisgrove SR, Simonich MT, Smith NM, Sattler NM, Innes RI. A disease resistance gene in Arabidopsis with specificity for two different pathogen avirulence genes. Plant Cell 1994;6:in press.
Dietrich RA, Delaney TP, Uknes SJ, Ward EJ, Ryals JA, Dangl JL. Arabidopsis mutants simulating disease resistance response. Cell 1994;77:565–578.
Dangl JL. The emergence of Arabidopsis thaliana as a model for plant-pathogen interactions. Adv. Plant Pathology 1993;10:127–155.
Feldmann KA. T-DNA insertion mutagenesis in Arabidopsis: mutational spectrum. Plant J. 1991;1:71–82.
Feldmann KA. T-DNA insertion mutagenesis in Arabidopsis: Seed transformation method. In: Koncz C, Chua N-H, Schell J, ed. Methods in Arabidopsis Research. Singapore: World Scientific, 1992: 274–289.
Walbot V, Hoisington DA, Neuffer MG. Disease lesion mimics in maize. In: Kosuge T, Meredith C, ed. Genetic Engineering of Plants. New York: Plenum Publishing Co., 1983: 431–442. (Hollander A, ed. vol 3).
Johal GS, Hulbert SH, Briggs SP. Disease lesion mimics of maize: A model for cell death in plants. Bioessays 1994; in press.
Greenberg JT, Ausubel FM. Arabidopsis mutants compromised for the control of cellular damage during pathogenesis and aging. Plant J. 1993;4:327–342.
Greenberg JT, Guo A, Klessig DF, Ausubel FM. Programmed cell death in plants: A pathogen-triggered response activated coordinately with multiple defense functions. Cell 1994;77:551–564.
Koch E, Slusarenko AJ. Arabidopsis is susceptible to infection by a downy mildew fungus. Plant Cell 1990;2:437–445.
Koch E, Slusarenko AJ. Fungal pathogens of Arabidopsis thaliana (L.) Heynh. Bot. HeIv. 1990;100:257–269.
Holub EB, Beynon JL, Crute IR. Phenotypic and genotypic characterization of interactions between isolates of Peronospora parasitica and accessions of Arabidopsis thaliana. Mol- Plant-Microbe Interact. 1994;7:223–239.
Liang P, Pardee A. Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction. Science 1992;257:967–971.
Liang P, Averbough L, Pardee AB. Distribution and cloning of eukaryotic mRNAs by means of differential display: refinements and optimizaton. Nucl. Acids Res. 1993;21:32693275.
Bauer B, Müller H, Reich J, et al. Identification of differentially expressed mRNA species by an improved display technique (DDRT-PCR). Nucl. Acids Res. 1993;21:4272–4280.
Metan M, Dong X, Endara ME, Davis KR, Ausubel FM, Peterman TK. An Arabidopsis thaliana lipoxygenase gene can be induced by pathogens, abscisic acid, and methyl jasmonate. Plant Physiol. 1993;101:441–450.
Manoil C, Beckwith J. TnphoA: A transposon probe for protein export signals. Proc. Natl. Acad. Sci., USA 1985;82:8129–8133.
Innes RW, Bent AF, Kunkel BN, Bisgrove SR, Staskawicz BJ. Molecular analysis of avirulence gene avrRpt2 and identification of a putative regulatory sequence common to all known Pseudomonas syringae avirulence genes. J. Bacteriol. 1993;175:4859–4869.
Shen H, Keen NT. Characterization of the promoter of avirulence gene D from Pseudomonas syringae pv. tomato. J. Bacteriol. 1993;175:5916–5924.
Niepold F, Anderson D, Mills D. Cloning determinants of pathogenicity from Pseudomonas syringae pathovar syringae. Proc. Natl. Acad. Sci., USA 1985;82:406–410.
Mukhopadhyay M, Williams J, Mills D. Molecular analysis of a pathogenicity locus in Pseudomonas syringae pv. syringae. J. Bacteriol. 1988;170:5479–5488.
Loubens L, Debarbieux L, Bohin A, Lacroix J-M, Bohin J-P. Homology between a genetic locus (mdoA) involved in the osmoregulated biosynthesis of periplasmic glucans in Escherichia colt and a genetic locus (hrpM) controlling pathogenicity in Pseudomonas syringae. Mol. Microbiol. 1993;10:329–340.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1994 Springer Science+Business Media Dordrecht
About this chapter
Cite this chapter
Dangl, J. et al. (1994). Plant and Pathogen Loci Determining Recognition and Cell Death in Arabidopsis Thaliana.. In: Daniels, M.J., Downie, J.A., Osbourn, A.E. (eds) Advances in Molecular Genetics of Plant-Microbe Interactions. Current Plant Science and Biotechnology in Agriculture, vol 21. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-0177-6_42
Download citation
DOI: https://doi.org/10.1007/978-94-011-0177-6_42
Publisher Name: Springer, Dordrecht
Print ISBN: 978-94-010-4079-2
Online ISBN: 978-94-011-0177-6
eBook Packages: Springer Book Archive