Plant pathogens and integrated defence responses to infection
By Jeffery L. Dangl, Jonathan D. G. Jones. Nature, 2001
4,108 citations recorded by the source corpus.
Subfields: Plant Science
View Paper: https://www.semanticscholar.org/paper/6adf22736658f1e86c1447c9c0656f626706af7b
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In Plant Science
Citations in the corpus
- Recombination is suppressed in an alien introgression in peanut harboring Rma, a dominant root-knot nematode resistance gene (2010, background): “…a recognition-dependent disease resistance (R) gene belonging to one of the many known R-gene classes in plants, e.g., the superfamily of nucleotide binding site (NBS) leucine-rich repeat (LRR) encoding Rgenes (Meyers et al. 1999, 2003; Dangl and Jones 2001; Staskawicz 2001; Chisholm et al. 2006).”
- Receptor-like cytoplasmic kinases integrate signaling from multiple plant immune receptors and are targeted by a Pseudomonas syringae effector. (2010, background): “PBS1 may be an operational virulence target (van der Hoorn and Kamoun, 2008) that has evolved into a molecular sensor of AvrPphB (Dangl and Jones, 2001).”
- The Physiological, Biochemical and Molecular Roles of Brassinosteroids and Salicylic Acid in Plant Processes and Salt Tolerance (2010, background): “Many of these defense-related genes have been shown to be directly or indirectly involved in the synthesis of SA (Dangl and Jones, 2001; Metraux, 2002).”
- Type III secretion system effector proteins: double agents in bacterial disease and plant defense. (2004, background): “The guard hypothesis, which is central to this model, was proposed six years ago to explain how the prevalent class of NBS-LRR R proteins recognize Avr proteins (47, 162).”
- Signal signature and transcriptome changes of Arabidopsis during pathogen and insect attack. (2005, positive): “…by microbial pathogens and herbivorous insects, plants have evolved sophisticated defensive strategies to “perceive” attack by pathogens and insects, and to translate this “perception” into an appropriate defensive response (Dangl and Jones 2001; Dicke and Hilker 2003; Pieterse and Van Loon 2004).”
- Coffee resistance to the main diseases: leaf rust and coffee berry disease (2006, background): “…actin cytoskeleton involvement, changes in the levels of a subset of transcripts (Grant and Mansfield 1999; Guest et al., 1999; Heath, 2000a, Dangl and Jones, 2001; Peck, 2003), involvement of plasma-membrane-bound NADPH oxidases, cell-wall-bound peroxidases, amino oxidases in the apoplast…”
- Fitness costs of R-gene-mediated resistance in Arabidopsis thaliana (2003, background): “The second hypothesis is that basal levels of RPM1 indirectly induce plant defence responses as a consequence of interactions with other R-proteins, the targets they guard, and the bacterial effectors (Avr proteins) they recogniz”
- Characterization of the wheat-Stagonospora nodorum disease system: what is the molecular basis of this quantitative necrotrophic disease interaction?† (2010, methodology): “The gene-for-gene model was originally described by Flor (1956) using the flax rust interaction and later refined and expanded by a huge collection of research that has assembled a model for many biotrophic systems (reviewed by HammondKosack & Jones, 1996; Dangl & Jones, 2001).”
- Elicitors, effectors, and R genes: the new paradigm and a lifetime supply of questions. (2007, background): “Earlier findings about R genes have been widely reviewed (19, 39, 53, 69, 88).”
- The perspectives of polygenic resistance in breeding for durable disease resistance (2002, background): “This resistance is the most studied and well-known defence mechanism and dozens of race specific resistance genes have been isolated ( Dangl & Jones, 2001 ).”
- Recent Molecular and Genomic Studies on Stress Tolerance of Forage and Turf Grasses (2006, background): “Biotic stresses are caused by organisms such as bacteria, fungi, insects, nematodes, and viruses (Dangl and Jones, 2001).”
- Elicitor recognition, signal transduction and induced resistance in plants (2012, background): “The rice R gene Xa-21 combines the features of the second and third groups with an extracellular LRR domain and a cytoplasmic serine/threonine protein kinase (Dangl and Jones 2001 ).”